CATALOGUE OF GENE SYMBOLS FOR WHEAT:  2004 Supplement

 

R.A. McIntosh1, K.M. Devos2, J. Dubcovsky3 and W.J. Rogers4

 

1Plant Breeding Institute, The University of Sydney, 107 Cobbitty Road, Cobbitty, N.S.W., Australia, 2570.

2Departments of Crop and Soil Sciences, and Plant Biology, University of Georgia, Athens, GA 30602, U.S.A.

3Department of Agronomy and Range Science, University of California, Davis, CA 95616, U.S.A.

4Facultad de Agronomía, Universidad Nacional del Centro de la Provincia de Buenos Aires, C.C. 47, (7300) Azul, Argentina.

The most recent edition of the Catalogue, produced and presented at the 10th International Wheat Genetics Symposium is available on CD.  MacGene was produced by Y. Yamazaki in collaboration with R.A. McIntosh.  The Catalogue is also displayed on the GrainGenes Website: http://wheat.pw.usda.gov .

 

INTRODUCTION

1. Recommended Rules for Gene Symbolisation in Wheat

2.2.  Add:  'Where a molecule is composed of sub-units produced by different genes, a further capital letter may be added to the basic symbol to describe a particular sub-unit; for example, AhasL refers to a large sub-unit of the complex enzyme acetohydroxyacid synthase.'.

6.2.2.  Add to end of existing entry:  'R2 values, where given, indicate the proportion of variation explained by a QTL.'.

12.  Add to this rule: 'The entire sequence (134.540 bp) and a genetic map of the circular wheat chloroplast genome is provided in {10036}.  A total of 30 tRNA genes and 75 protein-encoding genes were identified.'.

 

9. Laboratory Designators for DNA markers

 

eco

Fedak, G.

fedakga@agr.gc.ca

Eastern Cereal and Oilseed* Research Centre,

Agriculture and Agri-Food Canada,

960 Carling Ave, Building 50,

Ottawa, ON K1A 0C6,

Canada

 

cfa

(T. monococcum clones)

Sourdille, Pierre

sourdil@clermont.inra.fr

UMR Amelioration et Sante des Plantes,

Domaine de Crouelle,

234, Avenue du Brezet,

63039, Clermont-Ferrand,

Cedex 2,

France

 

 

fwm

Sourdille, Pierre

sourdil@clermont.inra.fr

UMR Amelioration et Sante des Plantes,

Domaine de Crouelle,

234, Avenue du Brezet,

63039, Clermont-Ferrand,

Cedex 2,

France

 

nau

Chen, Piedu,

pdchen@njau.edu.cn

Cytogenetics Institute,

Nanjing Agricultural University,

Nanjing,

Jiangsu, 210095,

China

 

pur

Ohm, H.

hohm@purdue.edu

Department of Agronomy,

Purdue University,

West Lafayette,

IN, 47907-2054,

USA

 

umn

Muehlbauer, G.

muehl003@umn.edu

Department of Agronomy and Plant Genetics,

University of Minnesota,

St Paul,

MN,

USA

 

wgp

Chen, Xianming

xianming@mail.wsu.edu

USDA-ARS,

Department of Plant Pathlogy,   

Washington State University, Pullman,   

Washington 99164-6430                   

U.S.A.  

 

10. Organisation of the Catalogue

4. Stock listings:

After tv2: add new group: sutv: = Chromosome substitutions into tetraploid wheat.

 

DNA Markers

Add at end of introductory section:

‘Approximately 8000 ESTs have been mapped on a set of 101 deletion lines, containing 159 deletions distributed over the 42 wheat chromosome arms.  The allocation of these ESTs to chromosome ‘bins’ can be viewed on http://wheat.pw.usda.gov/NSF/progress_mapping.html.  Manuscripts resulting from this work include {10041} and {10042}.’

 

Group 1S

Add:

XBmac0213-1R {10081}.

 

Barley SSR.

 

Xcfd61-1A {10071}.

 

CFD 61 F/CFD 61 R.

 

Xeco406-1A,B,D {10047}.

 

Ta01_04b06.

 

Xiag95-1R {10081,10074}.

 

STS marker.

 

Xksu946(NBS-LRR)-1A,B,D {10052}.

 

KSU946.

(2B, 3A).

Xksuk951(Kin)-1D {10052}.

 

KSUK951.

(1A, 1BL, 3D, 6D, 7B).

Xpsr960-1R {10081}.

 

PSR960.

 

XSCM9-1R {10081}.

 

Rye SSR.

 

 

Group 1L

Add:

Xcdo346-1A {10071}.

 

CDO346.

 

Xeco702-1A,B {10047}.

 

Ta01_07h02.

 

Xeco812-1D {10047}.

 

Ta01_08f12.

(6A,B,D).

Xfbb275-1A {10071}.

 

FBB275.

 

Xgwm601-1A {10071}.

 

WMS 601 F/WMS601 R.

 

Xksuk951(Kin)-1B {10052}.

 

KSUK951.

(1A, 1DS, 3D, 6D, 7B).

 

Group 1

Add:

Xbcd1514-1A {10048}.

 

BCD1514.

 

Xbcd1562-1A {10048}.

 

BCD1562.

 

Xbcd1930-1B {10048}.

 

BCD1930.

 

Xcfd92-1D {10071}.

 

CFD 92 F/CFD 92 R.

 

Xfba118-1B {10048}.

 

FBA118.

 

Xfba165-1B {10048}.

 

FBA165.

 

Xfba294-1A {10048}.

 

FBA294.

 

Xfba298-1B {10048}.

 

FBA298.

 

Xfbb90-1A {10048}.

 

FBB90.

 

Xfbb160-1D {10048}.

 

FBB160.

 

Xfbb190-1A {10048}.

 

FBB190.

 

Xfbb196-1B {10048}.

 

FBB196.

 

Xfbb278-1A,B {10048}.

 

FBB278.

 

Xksu36-1A,D {10048}.

 

AFLP-36F/AFLP-36R.

 

Xksu940(NBS-LRR)-1A,B,D {10052}.

 

KSU940.

 

Xksu941(NBS-LRR)-1B,D {10052}.

 

KSU941.

 

Xksu942(NBS-LRR)-1B,D {10052}.

 

KSU942.

 

Xksu945(NBS-LRR)-1B {10052}.

 

KSU945.

(2D).

Xksuk950(Kin)-1A,B,D {10052}.

 

KSUK950.

 

Xksuk951(Kin)-1A {10052}.

 

KSUK951.

(1BL, 1DS, 3D, 6D, 7B).

Xksuk955(Kin)-1D {10052}.

 

KSUK955.

(2B, 5A,D, 6A,B).

Xksuk959(Kin)-1A,B {10052}.

 

KSUK959.

(4B).

Xksuk963(Kin)-1D {10052}.

 

KSUK963.

(2B, 3B,D, 5D).

Xksuk969(Kin)-1D {10052}.

 

KSUK969.

 

Xksuk970(Kin)-1A {10052}.

 

KSUK970.

(3B, 5D).

Xksuk971(Kin)-1D {10052}.

 

KSUK971.

(2D, 3A, 7B).

Xnau1(NBS)-1A,B {10084}.

 

RGA WN20.

 

Wag-1A, B, D {10078}.                                               {10078}

 

Probe 386-bp of the 3’ end of GenBank accession AB084577.

 

 

Group 2S

Amendments:

Xgdm5-2A.  Change the first column to ‘Xgdm5-2A {0173}, 2D {10055}.’.

Xpsr102(Sam)-2A,B,D. Add: ‘The development of locus-specific primers for the A, B and D loci was reported in {0049}.’.

Xpsr112-2A,B,D. Add:  ‘The development of locus-specific primers for the A, B, D and R loci was reported in {0049}.’.

 

Add:

Xbcd348-2N {10073}.

 

BCD348.

 

Xcmwg682-2N {10073}.

 

CMWG682.

 

Xeco509-2A,B,D {10047}.

 

Ta01_05h09.

(7A,B,D).

Xfbb67-2B {10071}.

 

FBB67.

 

Xgwm400-2A{10071}.

 

WMS 400 F/WMS 400 R.

 

Xgwm429-2B {10071}.

 

WMS 429 F/WMS 429 R.

 

Xgwm682-2B {10055}.

 

WMS F682/WMS R682.

 

Xgwm726-2A {10047}.

 

WMS F726/WMS R726.

 

Xgwm830-2A {10055}.

 

WMS F830/WMS R830.

 

Xgwm886-2D {10055}.

 

WMS F886/WMS R886.

 

Xgwm895-2A {10055}.

 

WMS F895/WMS R895.

 

Xgwm1045-2A {10055}.

 

WMS F1045/WMS R1045.

 

Xgwm1052-2A {10055}.

 

WMS F1052/WMS R1052.

 

Xgwm1115-2A {10055}.

 

WMS F1115/WMS R1115.

 

XHak2-2A {9932,10073}.

 

HvHAK2.

 

Xgwm1128-2B {10055}.

 

WMS F1128/WMS R1128.

 

XksuH9-2N {10073}.

 

KSUH9.

 

XksuD18-2N {10073}.

 

KSUD18.

 

Xpsr150-2N {10073}.

 

PSR150.

 

 

Xpsr933.1-2N {10073}.

 

PSR933.

 

 

Xvrga1-2N {0213,10073}.

 

VRGA1.

 

 

5.Group 2L

Add:

Xcsl107-2B {10013}.

 

G4-5', G035-5', G035-3'.

(2D).

Xcsl107-2D {10013}.

 

G4-5', G035-5', G035-3'.

(2B).

Xeco203-2A,B,D {10047}.

 

Ta01_02b03.

 

Xeco208(L38)-2D {10047}.

 

Ta01_02g08.

 

Xfba259-2B {10071}.

 

FBA259.

 

Xgwm761-2A {10055}.

 

WMS F761/WMS R761.

 

Xgwm940-2B [{10055}].

[Xgwm940a-2B {0455}].

WMS F940/WMS R940.

 

Xgwm1027-2B {10055}.

 

WMS F1027/WMS R1027.

 

Xgwm1204-2D {10055}.

 

WMS F1204/WMS R1204.

 

Xgwm1249-2B {10055}.

 

WMS F1249/WMS R1249.

 

Xgwm1256-2A {10055}.

 

WMS F1256/WMS R1256.

 

Xgwm1264-2D {10055}.

 

WMS F1264/WMS R1264.

 

Xksu944(NBS-LRR)-2A {10052}.

 

KSU944.

(5D).

Xksu946(NBS-LRR)-2B {10052}.

 

KSU946.

(1A,B,D, 3A).

XksuK965(Kin)-2A,B {10052}.

 

KSUK965.

 

Note: The location of the XksuK965-2A locus was ambiguous as the same fragment was missing in both N5B and N2A.  It is likely, however, that the absence of the fragment in N5B was caused by rearrangements due to the absence of Ph1 {10053}.

Xwmc474-2B {10055}.

 

WMC 474F/WMC 474R.

(2A).

Xwmc477-2B {10055}.

 

WMC 477F/WMC 477R.

 

Xwgp17(Rga)-2B  {10117}.

 

S2/AS3.

 

Xwgp18(Rga)-2B

{10117}.

 

S2/AS3.

 

Xwgp19(Rga)-2B {10117}.

 

RLRR Rev/LM638.

 

Xwgp20(Rga)-2B {10117}.

 

RLRR Rev/LM638.

 

Xwgp21(Rga)-2B {10117}.

 

Pto kin11N/Pto kin21N.

 

Xwgp22(Rga)-2B {10117}.

 

Cr33LR-R/Pto kin2.

 

Xwgp23(Rga)-2B {10117}.

 

Cr33LR-R/Pto kin2.

 

Xwgp24(Rga)-2B {10117}.

 

Xa1LR-F/Pto kin4.

 

Xwgp25(Rga)-2B {10117}.

 

XLRR Rev/Pto kin1.

 

Xwgp26(Rga)-2B {10117}.

 

Pto kin2/AS3-INV.

 

Xwgp27(Rga)-2B {10117}.

 

CLRR-INV2/Pto kin1.

 

Xwgp28(Rga)-2B {10117}.

 

RLRR Rev/Pto kin4.

 

Xwgp29(Rga)-2B {10117}.

 

RLK-Rev/Xa1 NBS-F.

 

Xwgp30(Rga)-2B {10117}.

 

LM638/S2.

 

Xwgp31(Rga)-2B {10117}.

 

Pto kin2/RLK-For.

 

Xwgp32(Rga)-2B {10117}.

 

Pto kin2/NLRR-INV1.

 

 

Group 2

Add:

Xfbb255-2B{10069}.

 

FBB255.

 

Xgwm448-2D {10071}.

 

WMS 448 F/ WMS 448 R.

 

Xgwm496-2D {10085}.

 

WMS 496 F/ WMS 496 R.

 

Xgwm817-2A {10031}.

 

WMS F817/WMS R817.

 

Xksu945(NBS-LRR)-2D {10052}.

 

KSU945.

(1B).

XksuK948(Kin)-2A,B,D {10052}.

 

KSUK948.

 

Note: The location of the XksuK948-2A locus was ambiguous as the same fragment was missing in both N5B and N2A.  It is likely, however, that the absence of the fragment in N5B was caused by rearrangements due to the absence of Ph1 {10053}.

Xksuk955(Kin)-2B {10052}.

 

KSUK955.

(1D, 5A,D, 6A,B).

Xksuk963(Kin)-2B {10052}.

 

KSUK963.

(1D, 3B,D, 5D).

Xksuk971(Kin)-2D {10052}.

 

KSUK971.

(1D, 3A, 7B).

Xnau2(NBS)-2A,D {10084}.

 

 

RGA N9.

 

 

Xwmc474-2B {10067}.

 

WMC474F/WMC474R.

 

 

Xwmc499-2B {10067}

 

WMC499F/WMC499R

 

 

Group 3S

Add:

Xbarc12-3A {10044}.

 

BARC 12F/BARC 12R.

 

Xbarc57-3A {10044).

 

BARC 57F/BARC 57R.

 

Xbarc86-3A {10044}.

 

BARC 86F/BARC 86R.

 

Xcfd79-3A {10071}.

 

CFD 79 F/CFD 79 R.

 

Xcmwg680-3A {10044).

 

cMWG680.

 

Xgwm892-3D {10055}.

 

WMS F892/WMS R892.

 

Xgwm1034-3B {10076}.

 

WMS 1034 F/WMS 1034 R.

 

Xwmc505-3A {10067}.

 

WMC505F/WMC505R.

 

 

Group 3L

Add:

Xfwm-3B {10080}.

 

FWM 4 F / FWM 4 R.

 

Xeco604(Glb3)-3A,B,D {10047}.

 

Ta01_06f04.

 

Xgwm234-3B {10071}.

 

WMS 234 F / WMS 234 R.

 

Xgwm344-4A {10071}.

 

WMS 344 F / WMS 344 R.

 

Xgwm1088-3D {10055}.

 

WMS F1088/WMS R1088.

 

Xksu946(NBS-LRR)-3A {10052}.

 

KSUK946.

(1A,B,D, 2B).

Xwmc322-3A {10067}.

 

WMC322F/WMC322R.

 

 

Xwmc56-3B {10067}.

 

WMC56F/WMC56R.

 

 

 

Group 3

Add:

Xksuk951(Kin)-3D {10052}.

 

KSUK951.

(1A,B,D, 6D, 7B).

Xksuk953(Kin)-3B {10052}.

 

KSUK953.

(6A,B,D).

Xksuk954(Kin)-3A,B,D {10052}.

 

KSUK954.

 

Xksuk963(Kin)-3B,D {10052}.

 

KSUK963.

(1D, 2B, 5D).

Xksuk967(Kin)-3D {10052}.

 

KSUK967.

(5B).

Xksuk970(Kin)-3B {10052}.

 

KSUK970.

(1A, 5D).

Xksuk971(Kin)-3A {10052}.

 

KSUK971.

(1D, 2D, 7B).

 

Group 4S (4AL:4BS:4DS)

Add:

Xeco903(a-Tub)-4A,B,D {10047}.

 

Ta01_09a03.

(6A)

Note: {10047} states that marker Ta01_09a03 detects loci on 4AS, 4BS, 4DS.  Most likely, this should read 4AL, 4BS, 4DS.

Xeco901(L2)-4A,B,D {10047}.

 

Ta01_09f01.

(5A,B,D).

Note: {10047} states that marker Ta01_09a03 detects loci on 4AS, 4BS, 4DS.  Most likely, this should read 4AL, 4BS, 4DS.

Xgwm742-4A {10055}.

 

WMS F742/WMS R742.

 

Xgwm832-4A {10055}.

 

WMS F832/WMS R832.

 

Xgwm894-4A {10055}.

 

WMS F894/WMS R894.

 

Xgwm959-4A {10055}.

 

WMS F959/WMS R959.

 

 

Group 4L (4AS:4BL:4DL)

Add:

XBx1-4A,B,D [{10103}].

[TaBx1-4A,B,D {10103}].

Primers based on maize Bx1.

 

XBx2-4A,B,D [{10103}].

[TaBx2-4A,B,D {10103}].

Primers based on maize Bx1.

 

Xgwm929-4A {10055}.

 

WMS F929/WMS R929.

 

Xpsr103-4AL {10080}.

 

PSR103.

 

XksuG30-4BL{10080}.

 

KSUG30.

 

Xgwm1093-4A {10055}.

 

WMS F1093/WMS R1093.

 

 

Group 4

Add:

Xksu943(NBS-LRR)-4B {10052}.

 

KSU943.

 

Xksuk958(Kin)-4A {10052}.

 

KSUK958.

(5B, 6B).

Xksuk959(Kin)-4B {10052}.

 

KSUK959.

(1A,B).

 

Group 5S

Add:

Xbarc56-5A {10076}.

 

BARC 56 F/BARC 56 R.

 

XBx3-5A,B.1,D [{10103}].

[TaBx3-5A,B,D {10103}].

Primers based on maize Bx3.

(5BL).

XBx4-5A,B,D [{10103}].

[TaBx4-5A,B,D {10103}].

Primers based on maize Bx4.

 

XBx5-5A,B.1,D [{10103}].

[TaBx5-5A,B,D {10103}].

Primers based on maize Bx5.

(5BS).

XBx5-5B.2 [{10103}].

[TaBx5-5B {10103}].

 

(5BS).

Xeco608-5A {10047}.

 

Ta01_06h08.

(6B, 7B).

Xeco901(L2)-5A,B,D {10047}.

 

Ta01_09f01.

(4A,B,D).

Xgwm1057-5A {10076}.

 

WMS 1057 F/WMS 1057 R.

 

Xksuk960(Kin)-5B {10052}.

 

KSUK960.

(6B, 7A,B,D).

 

Group 5L

Add:

XBx3-5B.2 [{10103}].

[TaBX3-5B {10103}].

Primers based on maize Bx1.

(5AS,BS,DS).

Xcfa255-5A {10071}.

 

CFA 255 F/ CFA 255 R.

 

Xcfa2155-5A {10080}.

 

CFA 2155 F/CFA 2155 R.

 

Xcfa2163-5A {10080}.

 

CFA 2163 F/CFA 2163 R.

 

Xfbb166-5A {10080}.

 

FBB166.

 

Xgwm271-5A {10071}.

 

WMS 271 F/WMS 271 R.

 

Xgwm810-5B {10007}.

 

WMS F810/WMS R810.

 

Xksu944(NBS-LRR)-5D {10052}.

 

KSU944.

(2A).

Xksuk952(Kin)-5A {10052}.

 

KSUK952.

(5B,D, 6A,B).

XksuP16-5A {0048}.

 

pTtksuP16.

 

Xgwm843-5B {10056}.

 

WMS F843/WMS R843.

 

Xgwm1016-5B {10007}.

 

WMS F1016/WMS R1016.

 

Xgwm1043-5B {10007}.

 

WMS F1043/WMS R1043.

 

Xmwg2062-5A {10079}.

 

MWG2062.

 

Xgwm1180-5B{10007}.

 

WMS F1180/WMS R1180.

 

XSnf2P-5A {10098}.

 

Complete sequence from BAC AY485644.

 

Xucw1(Nuc)-5A {10098}.

 

UCW1 (Barley Nucellin gene).

 

Xucw2-5A {10098}.

 

UCW2.

 

Xucw26-5A {10109}.

 

UCW26.

 

Xucw90(Cbf3)-5A {10079}.

[XCbf3 {10079}].

Barley CBF3.

 

 

Group 5

Add:

Xgwm271-5A {10069}.

 

WMS271F/WMS271R.

 

Xksuk952(Kin)-5A,B,D {10052}.

 

KSUK952.

(6A,B).

Xksuk955(Kin)-5A,D {10052}.

 

KSUK955.

(1D, 2B, 6A,B).

Xksuk956(Kin)-5A,B {10052}.

 

KSUK956.

 

Xksuk957(Kin)-5A,B,D {10052}.

 

KSUK957.

 

Xksuk958(Kin)-5B {10052}.

 

KSUK958.

(4A, 6B).

Xksuk963(Kin)-5D {10052}.

 

KSUK963.

(1D, 2B, 3B,D).

Xksuk967(Kin)-5B {10052}.

 

KSUK967.

(3D).

Xksuk968(Kin)-5B {10052}.

 

KSUK968.

(6B).

Xksuk970(Kin)-5D {10052}.

 

KSUK970.

(1A, 3B).

Xksuk972(Kin)-5B,D {10052}.

 

KSUK972.

 

Xksuk973(Kin)-5B {10052}.

 

KSUK973.

 

Xmta15-5A{10069}.

 

MTA15.

 

Xnau3(NBS)-5B,D {10084}.

 

RGA N9.

 

Xnau4(NBS)-5B {10084}.              

 

RGA WN16.

 

 

Group 6S

Add:

Xeco608-6B {10047}.

 

Ta01_06h08.

(5A, 7B).

Xeco812-6A,B,D {10047}.

 

Ta01_08f12.

(1D).

Xeco903(a-Tub)-6A {10047}.

 

Ta01_09a03.

(4A,B,D).

Xgwm680-6B {10055}.

 

WMS F680/WMS R680.

 

Xgwm771-6B {10055}.

 

WMS F771/WMS R771.

 

Xgwm825-6B {10055}.

 

WMS F825/WMS R825.

 

Xgwm889-6B {10055}.

 

WMS F889/WMS R889.

 

Xgwm935-6B {10060}.

 

WMS F935/WMS R935.

(7B).

Xgwm1255-6B {10055}.

 

WMS F1255/WMS R1255.

 

Xksuk953(Kin)-6B {10052}.

 

KSUK953.

(6A,D, 3B).

Xksuk958(Kin)-6B {10052}.

 

KSUK958.

(4A, 5B).

Xksuk960(Kin)-6B {10052}.

 

KSUK960.

(5B, 7A,B,D).

 

26. Group 6L

Amendments:

Xcdo347-6B {0220}.     CDO347.     (7A,7D).

 

Add:

Xeco501-6A,B,D {10047}.

 

Ta01_05a01.

 

Xwmc182-6B {0348}.

 

WMC 182F/WMC 182R.

 

Xwmc341-6B {10067}.

 

WMC341F/WMC341R

 

 

Group 6

Add:

Xcdo347-6A,6B,6D (0220}.

 

CDO347.

(6A,B,D) (7A,D).

Xksuk949(Kin)-6B,D {10052}.

 

KSUK949.

(7A).

Xksuk951(Kin)-6D. {10052}.

 

KSUK951.

(1A,B,D, 3D, 7B).

Xksuk952(Kin)-6A,B {10052}.

 

KSUK952.

(5A,B,D).

Xksuk953(Kin)-6A,B,D {10052}.

 

KSUK953.

(3B).

Xksuk955(Kin)-6A,B {10052}.

 

KSUK955.

(1D, 2B, 5A,D).

Xksuk961(Kin)-6A,B {10052}.

 

KSUK961.

 

Xksuk966(Kin)-6A,B,D {10052}.

 

KSUK966.

 

Xksuk968(Kin)-6B {10052}.

 

KSUK968.

(5B).

 

 

Group 7S

Amendments:

Xgwm935-7B.  Add ‘(6B).’ in the last column.

 

Add:

Xcfd2-7D {10071}.

 

CFD 2 F/ CFD 2 R.

 

Xeco509-7A,B,D {10047}.

 

Ta01_05h09.

(2A,B,D).

Xeco608-7B {10047}.

 

Ta01_06h08.

(5A, 6B).

It is not known whether Xeco608-7B belongs to group 7S or to group 7AS:4AL:7DS.

Xgwm302-7A {10071}.

 

WMS 302 F / WMS 302 R.

 

Xgwm1014-7D {10055}.

 

WMS F1014/WMS R1014.

 

Xgwm1171-7A {10055}.

 

WMS F1171/WMS R1171.

 

 

7AS:4AL:7DS

Add:

Xksu947(NBS-LRR)-7A,4A {10052}.

 

KSU947.

 

Note: The location of the Xksu947 locus was ambiguous as the same fragment was missing in both N5B and N7A.  It is likely, however, that the absence of the fragment in N5B was caused by rearrangements due to the absence of Ph1 {10053}.

Xksuk962(Kin)-7A {10052}.

 

KSUK962.

 

 

Group 7L

Amendments:

Xcdo347-7A.    Add: ‘(6B)’ to the last column.

Xcdo347-7B     Add: ‘(6B)’ to the last column.

 

Add:

Xeco811(Gapd2)-7A,B,D {10047}.

 

Ta01_08d11.

 

Xgwm783-7B {0258}.

 

WMS 783 F/WMS 783 R.

 

Xgwm883-7B{0258}.

 

WMS 883 F/WMS 883 R.

 

Xgwm984-7B {0258}.

 

WMS 984 F/WMS 984 R.

 

Xgwm1144-7B {0258}.

 

WMS 1144 F/WMS 1144 R .

 

Xgwm1175-7B {0258}.

 

WMS 1175 F/WMS 1175 R.

 

Xgwm1267-7B {0258}.

 

WMS 1267 F/WMS 1267 R.

 

Xgwm1498-7B {0258}.

 

WMS 1498 F/WMS 1498 R.

 

Xwmc182-7B {10080}.

 

WMC182 F/WMC182 R.

 

Xwmc500-7B {10067}.

 

WMC500F/WMC500R.

 

 

Group 7

Add:

Xbcd1930-7A {10071}.

 

BCD1930.

 

Xksu23-7A,D {10050}.

 

AFLP-23F/AFLP-23R.

 

Xksuk949(Kin)-7A {10052}.

 

KSUK949.

(6B,D).

Xksuk951(Kin)-7B {10052}.

 

KSUK951.

(1A,B,D, 3D, 6D).

Xksuk960(Kin)-7A,B,D {10052}.

 

KSUK960.

(5B, 6B).

Xksuk964(Kin)-7A,B,D {10052}.

 

KSUK964.

 

Xksuk971(Kin)-7B {10052}.

 

KSUK971.

(1D, 2D, 3A).

 

Morphological and Physiological Traits

1. Gross Morphology: Spike Characteristics

1.2. Club/Compact spike

QTL: Two additional QTLs for spike compactness were detected in Courtot/Chinese Spring {10080} on chromosome arms 5DL (QCp.icf-5D) and 6DL (QCp.icf-6D). Markers Xcfd26-5D and Xcfd38-6D explained 13.6% and 12.2% of the variance in spike compactness, respectively {10080}.

 

6.Awnedness

6.1 Dominant inhibitors

6.1.2. Tipped 1

B1.     v:  WAWHT2046 {10040}.     ma: Xgwm6a-5A - 13.5cm - B1 - 12.2cM - Yr34 {10040}.

 

9. Brittle Rachis (revised section)

Br-A1{10061}.      [Br1 {9970}].         3DS{9970}.            v:  T. aestivum var. tibetanum{9970}.

Br-A2{10061}.      [Br2 {0130}].         3A{0130}.   3AS {10061}.   sutv:  LDN(DIC 3A){0130}.

Br-A3{10061}.      [Br3 {0130}].         3B{0130}.   3BS {10061}.    sutv:  LTN(DIC 3B){0130}.

 

 

Evidence for an orthologous series extending to many related species is discussed in {0130} and {10061}.

 

Br4 {10082}.     2A {10082}.     tv:  T. dicoccoides {10082}.    ma: 33 cM distal to Xgwm294-2A (LOD= 6.3, R2= 14.4%) {10082}.

 

11. Cadmium Uptake

11.1. Low cadmium uptake

Add the following:

Cdu1.     5BL {10104}.  v:  Kyle*2/Biodur (10104}.

cdu1.     v:  Kofa {10104}.

 

18. Ear Emergence

QTLs for ear emergence were detected in the cross Renan/Recital {10069}. LOD scores and percent of variation explained by the QTL (R2) are averages of three years of field tests.

 

QEet.inra-2B {10069}.                        ma: 2B linked to Xgwm148 (LOD= 5.7, R2= 11.9.2%).

QEet.inra-2D{10069}.                         ma: 2D linked to XksuE3 (LOD= 2.7, R2= 6.5%).

QEet.inra-7D {10069}.                        ma: 7D linked to Pch1 (LOD= 3.9, R2= 7.3%).

 

19. Earliness Per Se

Eps-5BL1 {10075}.      5BL (10074}.     ma: QTL mapped on chromosome 5BL, linked to Xwmc73-5B (this QTL explained 8% of the variance in flowering time, P<0.03) {10074}. 

 

Eps-5BL2 {10074}.       5BL {10074}.     ma: QTL mapped on chromosome 5BL, linked to Xgwm499-5B (this QTL explained 6% of the variance in flowering time) {10074}. 

 

QTLs

Two QTL for narrow-sense earliness were detected on chromosome 2B in a CS/T. spelta var. duhamelianum KT19-1 RI population {10057}.  The QTL were associated with markers Xpsr135-2B and Xabc451-2B {10057}.  For both QTL, earliness was conferred by the CS allele.

 

20. Flowering time

Insert at beginning of section:  ‘The isolation of wheat genes orthologous to the Arabidopsis Co and rice Hd1 gene was reported in {10054}.  The genomic clones TaHd1-1, TaHd1-2 and TaHd1-3 originate from the long arms of chromosomes 6A, 6B and 6D, respectively.  The orthology of the TaHd1 genes with Co/Hd1 has been demonstrated by complementation of a rice line deficient in Hd1 function with the TaHd1-1 genomic clone.  It should be noted that the wheat TaHd1 and rice Hd1 genes are located in non-syntenic locations {10054}.  To date, no variation for flowering time has been identified on the wheat group 6 chromosomes.’

 

23. Frost Resistance

Fr-A2 {10079}.     dv: Triticum monococcum. Frost tolerant parent G3116, frost susceptible parent DV92.     ma: The QTL mapped on chromosome 5AL has a LOD score of  9 and explained 49% of the variation in frost tolerance. Closest markers: Xbcd508-5A and Xucw90(Cbf3)-5A. These markers are 30 cM proximal to Xwg644-5A, which is closely linked to frost tolerance locus Fr-1. QTLs for frost tolerance in the Fr-2 region have been also identified in wheat chromosome 5B (Fr-B2 {10079}) and in barley chromosome 5H (Fr-H2 {10083}).

 

Fr-B2      [Fr-B1 {10075}].     ma: QTL mapped on chromosome 5BL, linked to Xgwm639-5B (this QTL explained 12-31% of the variance in frost tolerance) {10075}.  Xgwm639-5B mapped close to Xmwg914-5B, and to Xbcd508-5B, a marker located at the peak of the Fr-A2 QTL {10075}. This data suggests that this locus is more likely orthologous to Fr-2 than to Fr-1.

 

24.1. Gametocidal activity

Gc2-Sl1b.     ma: an EMS-induced Gc-2 mutant was mapped to a wheat-Aegilops sharonensis T4B-4Ssh#1 translocation chromosome {10068}.

 

28. Grain Hardness/Endosperm Texture

Add at end of section:  ‘QTL:  Two QTL were detected for grain hardness in RILs of the ITMI population (Synthetic / Opata 85) {10051}.  The QTL on the short arm of chromosome 5D is associated with Xmta10-5D, and increased hardness is contributed by Opata {10051}.  The locus located proximally on the long arm of 5D is associated with Xbcd450-5D and increased hardness is contributed by the Synthetic allele {10051}.’.

 

Add at the end of the section:

‘Using proteomic analysis of 2D-protein gels applied to 101 lines of the Opata/W-7984 (ITMI) RI mapping population, and after a preliminary study of a sub-group of these lines {10086}, 446 amphiphilic protein spots were resolved, 170 specific to either of the two parents and 276 common to both {10087}. An important category of these proteins comprises the puroindolines. Seventy-two loci encoding amphiphilic proteins were conclusively assigned to 15 chromosomes. At least one Protein Quantity Locus (PQL) was associated with each of 96 spots out of the 170 spots segregating; these PQL were distributed throughout the genome. The majority of the amphiphilic proteins were shown to be associated with plant membranes and/or play a role in plant defence against external invasions. Not only the puroindolines were associated with kernel hardness – a number of other amphiphilic proteins were also found to influence this trait.’

 

31. Grain Weight

Grain weight

QGw1.inra-2B {10071}.

 

v:

Renan/Recital; favourable allele from Renan {10071}.  (R2= 10.7 - 19.7%) {10071}.

 

ma:

Xgwm374-2B - Xgwm388-2B

 

QGw1.inra-5B {10071}.    

 

v:

Renan/Recital; favourable allele from Recital {10071}. (R2= 4.9 – 10.4%) {10071}.

 

ma:

Xgwm639-5B - Xgwm604-5B

 

QGw1.inra-7A {10071}. 

 

v:

Renan/Recital; favourable allele from Recital {10071}.  (R2= 5.2 – 10.3%) {10071}.

 

ma:

Xcfa2049-7A - Xbcd1930-7A (R2= 5.2 – 10.3%) {10071}.

 

39.3.  Reduced Height: QTL

QTLs for height detected in the cross Renan/Recital {10069}. LOD scores and percent of variation explained by the QTL (R2) are averages of three years of field tests.

 

QHt.inra-2B {10069}.

ma:

Associated with Xgwm249-2B  (LOD= 5.8, R2= 15.4%).

QHt.inra-4A {10069}.

ma:

Associated with Xfba243-4A (LOD= 6.5, R2= 15.0%).

QHt.inra-5A {10069}.

ma:

Associated with Xgwm639b-5A (LOD= 5.7, R2= 10.8%).

QHt.inra-6D {10069}.

ma:

Associated with Xcfd76-6D (LOD= 3.7, R2= 8.1%).

QHt.inra-7A {10069}.

ma:

Associated with Xcdo545-7A  (LOD= 3.2, R2= 7.7%).

 

QHt.riso-3A {10067}.

ma:

Mapped on the centromeric region between SSR markers Xwmc505-3A and Xwmc264-3A (LOD>6) {10067}.

 

40. Herbicide Response

40.4.  Imidazolinone resistance

Resistance alleles found in mutagenised populations were incompletely dominant and additive in effect {10099}. Resistance is due to single base pair changes in acetohydroxyacid synthase.

Imi1 {10099}.    

6DL {10101}.   

[AhasL-D1 {10101},Fs-4 {10100}].    

 

v:

BW755 = Grandin*3 / Fidel-FS-4 {10099}; CDS Teal IMI 1A {10099}; CDC Teal IMI 9A {10099}; CDC Teal IMI 10A = Fidel-FS-2 {10099}; Clearfield WHS Janz = Janz*4/Fidel-FS-2; Clearfield WHS Stiletto = Stiletto*3//Spear/ fidel-FS-3; Fidel-FS-2 = ATCC 40997{10100}.    

 

v2:

CDC Teal IMI 15A = PTA 3955 Imi3 {10099}.

 

Imi2 {10099}.   

6BL {10101}.    

[AhasL-B1 {10101}].    

 

v:

CDC Teal IMI 11A = PTA 3953 {10099}.

 

Imi3 {10099}.    

6AL {10101}.    

[AhasL-A1 {10101}].    

 

v2:

CDC Teal IMI 15A Imi3 {10099}.    

 

dv:

T. monococcum mutant EM2 (mutant of susceptible line TM23 {10102}.

Mutant EM2 has a serine to asparagine substitution near the carboxyl end of the enzyme. The same change has led to imidazolinone resistance in hexaploid wheat, rice and Arabidopsis {10102}.

 

57. Red grain Colour

Add at beginning of the preamble:  Red colour is probably due to the polyphenol compounds phlobaphene or proanthocyanidin, synthesised through the flavanoid pathway.  Himi & Noda {10107} provided evidence that the D genes were wheat forms of Myb-type transcription factors (Myb10-3A, Myb10-3B, Myb-3D).

 

61. Response to Vernalization

Add to genotype list following Vrn-A1a:

Triple Dirk F: Vrn-A1b Vrn-B1b Vrn-D1b Vrn-D5a: Yes

Triple Dirk C: Vrn-A1b Vrn-B1b Vrn-D1b Vrn-D5b: Yes     Winter type.

 

Vrn-1.  Add to end of first section.

Diploid wheat:

Vrn1 {10014}.    

Spring type.

v:

G2528 (10014}.

vrn1 {10014}.    

Winter type.

v:

DV 92 {10014}; G1777 {10014}; G3116 {10014}.    

 

ma:

Vrn1 was completely linked to MADS-box genes AP1 and AGLG1.  AP1was considered a better candidate than AGLG1 and differences between winter and spring genotypes appeared to be related to differences in the promoter region of AP1 {10014}.  The involvement of AP1 in vernalization response conditioned by Vrn-1 was also reported in {10019}.

 

Vrn-B1a.      Add  v:  T. spelta var. duhamelianum KT19-1 {10057}.     ma: Vrn-B1a - 1.6cM - Xwg644-5B - 2.5cM - Xgwm408-5B {10004}. Closely linked to Xgwm408-5B in Diamant I*/ Mironovskaya 808 5A // Bezostaya 1 {10007}. A close association of Vrn-B1 with Xcdo1326-5B was reported in {10057}.

 

Replace the current Vrn4 section with the following:

Vrn4.     After the second sentence in the comments following germplasm entries insert: ‘Goncharov {10108} confirmed the existence of Vrn4 but failed to confirm its location on chromosome 5D.’.

 

Vrn5 {10004}.  To date only Vrn-D5 has been detected.

Vrn-D5a [{10004}].    

[Vrn-D5 {10004}, Vrn4 {1172}].    

5D {10002}, 5DL {10004}.    

 

i:

Triple Dirk F.    

 

v2:

Gabo Vrn-B1a {1172}; IL47 Vrn-A1a {10005}. 

 

ma:

Xgdm3-5D - 11.5 & 4.5 cM - Vrn-D5a {10004}.

Eight land races with only Vrn-D5a were detected in {10003}; others combined Vrn-D5a with other Vrn genes. Stelmakh {1424} doubted the existence of Vrn-D5a. Goncharov {10108} confirmed the existence of Vrn-D5a but failed to confirm its location on chromosome 5D. References to additional studies are given in {1424}.

 

QTL:  Add:  ‘A QTL on chromosome 5BL was linked to Xgwm604-5B (this QTL explained 11% of the variance in flowering time) {10075}.’.

 

72. Yield Components

72.1. Grain weight

72.1.2. 1000-grain weight

QTkwt.unl-3A.1 {10044}.

3AS {10044}.

v:

Cheyenne/Cheyenne (Wichita 3A) RI mapping population {10044}; a higher kernel weight of 0.27g was contributed by Cheyenne and the QTL explained 12.7 % of the phenotypic variation {10044}.   The QTL coincided with QTLs for grain yield, kernel number per square meter and kernels per spike {10044}.

 

ma:

Associated with Xbarc12-3A and Xtam55-3A {10044}.

 

72.3. Grain number per spike

QKps.unl-3A.1 {10044}.

3AS {10044}.

v:

Cheyenne/Cheyenne (Wichita 3A) RI mapping population {10044}; a higher kernel number of 0.3 kernels was contributed by Wichita and the QTL explained 15.5 % of the phenotypic variation {10044}.   The QTL coincided with QTLs for grain yield, kernel number per square meter and 1000-kernel weight {10044}.

 

ma:

Associated with Xbarc12-3A {10044}.

QKps.unl-3A.2 [{10044}].

3A {10044}.

v:

Cheyenne/Cheyenne (Wichita 3A) RI mapping population {10044}; a higher kernel number of 0.3 kernels was contributed by Cheyenne and the QTL explained 9.5 % of the phenotypic variation {10044}.  

 

ma:

Associated with Xbcd141-3A {10044}.

 

72.9. Grain yield

QGyld.unl-3A.1 {10044}.

3AS {10044}.

v:

Cheyenne/Cheyenne (Wichita 3A) RI mapping population {10044}; a higher grain yield of 32 kg/ha was contributed by Wichita and the QTL explained 6.6 % of the phenotypic variation {10044}.  The QTL coincided with QTLs for kernel number per square meter, 1000-kernel weight and kernels per spike {10044}.

QGyld.unl-3A.2 {10044}.

3A {04100}.

v:

Cheyenne/Cheyenne (Wichita 3A) RI mapping population {10044}; a higher grain yield of 82 kg/ha was contributed by Wichita and the QTL explained 28.1 % of the phenotypic variation {10044}.  The QTL coincided with a QTL for kernel number per square meter {10044}.

 

ma:

Associated with Xbarc67-3A and Xbcd366-3A {10044}.

QYld.inra-7D {10071}.

 

v:

Renan/Recital {10071}.

 

ma:

 

Xcdf69-7D (R2= 3.7 – 15.7%).

 

72.10. Kernel number per square meter

QKpsm.unl-3A.1 {10044}.

3AS {10044}.

v:

Cheyenne/Cheyenne (Wichita 3A) RI mapping population {10044}; higher kernel number (170 kernels) was contributed by Wichita and the QTL explained 14.6 % of the phenotypic variation {10044}.   The QTL coincided with QTLs for grain yield, 1000-kernel weight and kernels per spike {10044}.

 

ma:

Associated with Xbarc12-3A {10044}.

QKpsm.unl-3A.2 {10044}.

3A {10044}.

v:

Cheyenne/Cheyenne (Wichita 3A) RI mapping population {10044}; higher kernel number (195 kernels) was contributed by Wichita and the QTL explained 19.1 % of the phenotypic variation {10044}.   The QTL coincided with a QTL for grain yield {10044}.

 

ma:

Associated with Xbarc67-3A {10044}.

 

72.11 Grain volume weight

QGvwt.unl-3A.1 [{10044}].

3A {10044}.

v:

Cheyenne/Cheyenne (Wichita 3A) RI mapping population {10044}; higher grain volume weight (+23 kg/hL)) was contributed by Wichita and the QTL explained 43.1 % of the phenotypic variation {10044}.   The QTL coincided with a QTL for spikes per square meter {10044}.

 

ma:

Associated with Xbcd1380-3A {10044}.

 

 

74.1. Grain protein content

Insert as a note before the first XGpc.ccsu entry:  ‘Thirteen QTL for grain protein content were identified in a RI population from the cross WL711 (low protein content) and PH132 (high grain protein content) {10055}.  The QTLs that were identified using more than one method or in more than one environment are listed below.  Also listed is a QTL that was identified in the mean over the four environments and was therefore deemed important {10055}.’.

Replace the existing entry for XGpcccsu-2D.

QGpc.ccsu-2B.1 {10055}.

2BL {10055}.

v:

WL711/PH132 RI mapping population {10055}; higher protein content was contributed by PH132 and the QTL explained 13.4% of the phenotypic variation {10055}. 

 

ma:

Associated with Xgwm1249-2B {10055}.

QGpc.ccsu-2D.1 {0015,10055}.

2DL {0015,10055}.

v:

WL711/PH132 RI mapping population {0015,10055}; higher protein content was contributed by PH132 and the QTL explained 19% {0015} and 14% {10055} of the phenotypic variation.

 

ma:

Associated with Xgwm1264-2D {10055}.

QGpc.ccsu-3D.1 {10055}.

3DS {10055}.

v:

WL711/PH132 RI mapping population {10055}; higher protein content was contributed by PH132 and the QTL explained 16.3% of the phenotypic variation {10055}.

 

ma:

Associated with Xgwm456-3D {10055}.

QGpc.ccsu-3D.2 {10055}.

3DS {10055}.

v:

WL711/PH132 RI mapping population {10055}; higher protein content was contributed by PH132 and the QTL explained 14% of the phenotypic variation {10055}.

 

ma:

Associated with Xgwm892-3D {10055}.

QGpc.ccsu-7A.1 {10055}.

7AS {10055}.

v:

WL711/PH132 RI mapping population {10055}; higher protein content was contributed by PH132 and the QTL explained 32.4% of the phenotypic variation {10055}.

 

ma:

Associated with Xgwm1171-7A {10055}.

QPro.inra-2A {10071}.

2A {10071}.

v:

Renan/Recital {10071}.

 

ma:

XksuD18-2A - Xgwm614-2A (R2= 4.4 - 8.9%) {10071}.

QPro.inra-3A {10071}.

3A {10071}.

v:

Renan/Recital {10071}.

 

ma:

Xcfd79-3A - Xfbb250-3A (R2= 4.1 – 8.3%) {10071}.

QPro.inra-4D {10071}.

4D {10071}.

v:

Renan/Recital {10071}.

 

ma:

Linked to Xcfd71-4D (R2= 4.6 – 10.3%) {10071}.

QPro.inra-7D {10071}.

7D {10071}.

v:

Renan/Recital {10071}.

 

ma:

Xcfd69-7D - Pch1 (R2= 6.4 – 10.4%) {10071}.

For QTLs conferring grain protein content detected in the cross Renan/Recital {10071}, only QTLs stable over at least 4 of the 6 locations are presented. Renan contributed the four alleles for high grain protein content.

 

74.2.22. NADH dehydrogenase

74.2.22.3. Ndh-3

Insert as a note following the Ndh-D3 entry:  ‘A Ndh locus, designated Nadhd2, was mapped 27 cM from Est-D10 in an Ae. tauschii F2 population derived from VIR-1954/VIR-1345 {10046}.  This locus may be homologous to Ndh-D3.’.

 

74.2.27. Catalase

A catalase locus, designated Cat2, was mapped 6 cM proximal to Aco-D2 in an Ae. tauschii F2 population derived from VIR-1954/VIR-1345 cross {10046}.  This locus may be orthologous to Cat-B1 {10046}. 

 

74.2.30. Benzoxinones

The putative role of benzoinones sets Bx-1 to Bx-5 is to catalyse the pathway Indole-3-glycerol phosphate to DIBOA. Primers designed from maize sequences were used to generate RT-PCR products utilised to screen a cDNA library from CS seedlings. Full-length cDNAs were heterologously expressed in yeast and the Bx gene products had enzymatic action. The Bx genes located by Southern analysis of CS deletion stocks occurred as clustered groups in homoeologous groups 4 (Bx-1, Bx-2) and 5 (Bx-3.1,.2, Bx-4, Bx-5) {10103}.

 

74.2.31. Acetohydroxyacid synthase (EC 4.1.3.18)

An orthologous series was mapped as the active target sites of imidazolinone herbicides.  See section 40.4.

 

AhasL-A1 [{10101}].    

[Imi3 {10099}].    

6AL {10101}.    

 

v2:

CDC Teal IMI 15A Imi3 {10099}.    

 

dv:

T. monococcum mutant EM2 (mutant of susceptible line TM23 {10102}.

 

AhasL-B1 [{10101}].    

[Imi2 {10099}].    

6BL {10101}.     

 

v:

CDC Teal IMI 11A = PTA 3953 {10099}.

 

AhasL-D1 [{10101}].    

[Imi1 {10099}].    

6DL {10101}.    

 

v:

BW755 = Grandin*3 / Fidel-FS-4 {10099}.

 

74.3. Endosperm storage proteins

 

74.3.1.1 Glu-1

In the preamble, in the sentence that reads ‘No 'y-type' protein from the Glu-A1 locus has been demonstrated in hexaploid wheat {1118}, although they are found in diploid wheats {1535,798}, and sequencing experiments have shown the presence of a terminating sequence inside the transcribed portion of the gene {373}.’, replace the last part of the sentence with ‘and sequencing experiments have shown the presence of two stop codons in the transcribed portion of the gene {10088}.’

 

Glu-B1

In the text that follows the Glu-B1 listing, after the sentence that reads ‘Possible low gene expression at Glu-B1 was noted for Glu-B1w, where subunits 6*+8* stain very faintly {1146}.’ (par 2), add the following text: ‘Many of the cultivars carrying the over-expressed subunit 7 encoded by Glu-B1al show %UPP values that transcend the normal range observed for cultivars that lack this subunit {10089}, which presumably is associated in some way with its unusually high amount in the grain. The underlying cause of the increased amount may be due to an increased transcriptional rate compared to other alleles, for which a known difference in promoter sequence compared to other alleles expressing normal levels of this subunit {10090} may be responsible.’

 

Glu-D1

Add:

Glu-D1bo [{10091}].

5’+12 {10091}.

v:

W958 {10091}.

Note: this putative new allele encodes two subunits that have very similar electrophoretic mobilities compared to subunits 5+12 encoded by Glu-D1h, but analysis using the specific PCR primers for Dx5 described in {10092} and {10093} shows that the x-type subunit of Glu-D1bo, provisionally denominated 5’ {10091}, does not appear to be the same protein as subunit 5 {10091}. Definitive evidence awaits sequencing information (See note to allele Glu-D1-1s).

Correction: in the opening words of the paragraph following the Glu-D1 listing, replace ‘Glu-D1 {421}’ with ‘Glu-D1k {421}’. Also, correct the spelling, from ‘arison’ to ‘arisen’, in the same phrase.

 

Glu-D1-1

Allele Glu-D1-r needs to be placed in the correct order.

Add:

Glu-D1-1s [{10091}].

5’ {10091}.

v:

W958 {10091}.

Note: this putative new allele encodes a subunit, provisionally denominated 5’ {10091}, that has a very similar electrophoretic mobility compared to subunit 5 encoded by Glu-D1-1d, but analysis using the specific PCR primers for Dx5 described in {10092} and {10093} shows that it does not appear to be the same protein as subunit 5 {10091}. Definitive evidence awaits sequencing information. (See note to allele Glu-D1bo).

 

Glu-R1

Add after the Glu-R1 listing:

‘Five new x-type subunits (plus the null allele) and four y-type subunits were reported in {10094}. They vary principally through duplications and deletions of the tri-, hexa- and nona-peptide motifs found in the central repetitive region of the subunits. Orthologous genes were found to be more closely related than paralogous genes, supporting the hypothesis that gene duplication occurred before Triticeae speciation {10095,10094}.’

 

Glu-B3

Add:

Glu-B3z [{10116}].

6.1 {10116}.

tv:

Buck Cristal {10116}.

Note: the designation of this protein (subunit 6.1) as an allele of Glu-B3 was deduced from its electrophoretic mobility and awaits confirmation through mapping studies.

 

74.3.2. Gliadins

Add in the gliadin preamble (par. 3) at the end of ‘… families of gliadin alleles and some of their relationships were described {9988}.’.

‘Twenty eight gamma-gliadin gene sequences from Genbank were grouped into nine subgroups in {10063}.  Primers were developed against some of the subgroups and the chromosomal location of the gamma-gliadin genes was determined {10063}.’.

 

Add at the end of the preamble:

‘A new family of low-molecular-weight gliadin genes located on groups 4 and 7 were reported in {10117}. They appear to influence rheological properties and seem to be closely related to the 17 kDa e hordein, important in beer foam stability.’

 

74.5.6 Waxy proteins

Add at end of first par:  A multiplex PCR assay for identifying waxy genotypes is described in {10032}.

Wx-A1b. 

v:

California {10032}; Shino {10032}; Sturdy {10032}.   

 

v2:

Mochi-Otome Wx-B1b WxD1b {10032}; Nebarigoshi {10032}.

 

Wx-B1b.    

v:

{10032}; Reward {10032}; Yukon {10032}.     

 

v2:

Mochi-Otome Wx-A1b Wx-D1b {10032}: Nebarigoshi Wx-A1b {10032}.

 

 

Wx-D1b.    

v2:

Mochi-Otome Wx-A1b Wx-B1b {10032}.

 

Correction - in the entry:

Wx-D1d {0118}.

v:

K107wx1{0118}; EMS mutants{0118}; One Iranian and one Italian accession {03101}.

‘K107wx1’ should read ‘K107Wx1’ and ‘EMS mutants’ should read ‘K107Wx2’.

 

74.5.8. Puroindolines and Grain Softness Proteins

Pina-D1

Pina-D1d.    

dv:

Change the entry 'TA2521' to 'TA2512'

 

Add:

Pina-D1g {03105}.    

dv:

Ae. tauschii TA1583 (GenBank AY252029) Pinb-D1a, Gsp-D1b {03105}.

Pina-D1h {10118}.    

v:

X. Aegilotriticum CIGM86.946-1B-0B-0PR-0B (GenBank AY573898) Pinb-D1o {10118}.

Pina-D1i {10018}.

v:

X. Aegilotriticum CIGM87.2784-1B-0PR-0B (GenBank AY573899) Pinb-D1k {10118}.

Pina-D1j {10118}.    

v:

X. Aegilotriticum CIGM88.1363-0B (GenBank AY573900) Pinb-D1o {10118}.

Pina-D1j {10118}.    

v:

X. Aegilotriticum CIGM88.1363-0B (GenBank AY573900) Pinb-D1o {10118}.

Pina-D1k {10077}.    

s:

CS*/Red Egyptian 5D substitution line, Pinb-D1q, Gsp-D1i {10077}.

This locus has a large deletion encompassing genes Pina-D1, Pinb-D1 and Gsp-D1. This allelic combination confers a harder kernel texture than Pina-D1a/Pinb-D1b {10077}.

 

Pinb-D1

Pinb-D1l {10119}.    

v:

GaoCheng 8901 {10119}.

Pinb-D1m {10118}.    

v:

X. Aegilotriticum CIGM87.2783-1B-0PR-0B (GenBank AY573901) Pina-D1c {10118}.

Pinb-D1n {10118}.    

v:

X. Aegilotriticum CIGM92.1708 (GenBank AY573902) Pina-D1d {10118}.

Pinb-D1o {10118}.    

v:

X. Aegilotriticum CIGM93.247 (GenBank AY573903) Pina-D1e {10118}.

Pinb-D1p {10121}.    

v:

Nongda 3213 {10121}; Nongda 3395 {10121}.

Pinb-D1q {10077}.    

s:

CS*/Red Egyptian 5D substitution line, Pina-D1k, Gsp-D1i {10077}.

This locus has a large deletion encompassing genes Pina-D1, Pinb-D1 and Gsp-D1. This allelic combination confers a harder kernel texture than Pina-D1a/Pinb-D1b {10077}.

 

Add at end of section: 'In T. monococcum the gene order was reported to be: tel - Gsp-1 - Pina - Pinb {0083,10122} whereas in Ae. squarrosa it was: tel - Gsp-1 - Pinb - Pina {10037}.'.

 

74.5.9. Grain softness protein

Gsp-D1i {10120}.     

v:

Yecora Rojo (GenBank AY255771) Pina-D1b, Pinb-D1a {10120}.

Gsp-D1j {10077}.    

s:

CS*/Red Egyptian 5D substitution line, Pina-D1k, Pinb-D1q {10077}.

This locus has a large deletion encompassing genes Pina-D1, Pinb-D1 and Gsp-D1 {10077}.

 

Pathogenic Disease/Pest Reaction

 

76. Reaction to Blumeria graminis 
76.1. Designated genes for resistance
Pm3b.  Add at end of entry: The isolation of Pm3b is reported in {10064}.  The Pm3b gene (Genbank accession number AY325736) is a coiled-coil NBS-LRR type of disease resistance gene {10064}.

Pm24.

ma:

Xgwm789-1D/Xgwm603-1D - 2.4cM - Pm24 - 3.6cm - Xbarc229-1D {10109}.

Delete the comment at the end of the section.

 

Pm32 {10025}.   

Derived from Ae. speltoides {10025}.   

1B = 1BL.1SS {10025}.   

 

v:

L501 = Rodina*6/ Aeg. speltoides {10025}.

 

MlTd1055 {10029}.    

tv:

T. dicoccoides 1055 {10029}.

 

78. Reaction to Diuraphis noxia 
Dn7.  Add: ma: Xbcd1434-1B – 1.4 cM – Dn7 – 7.4 cM – XksuD14-1B {10059}.

 

79. Reaction to Fusarium spp.

79.1.  Disease:  Fusarium head scab, scab.

Type II resistance   Insert this heading after the disease name.

QFhs.ndsu.3B.     Insert comment after gene entry:  'Associated mainly with resistance to fungal spread {10073}'.

ma:  Add at end of first paragraph: ‘QFhs.ndsu-3B from Sumai 3 was associated with microsatellite loci Xgwm533-3B and Xgwm274-3B in certain Sumai 3 derivatives {10062}. In  Ning 894037 the QTL has the same location and similar SSR bands to Sumai 3 {10085}. STS marker SRST.3B1 was mapped between Xgwm533-3B and Xgwm389-3B and associated with QFhs.ndsu-3B {10072}. QFhs.ndsu.3B was associated with markers Xgwm533-3B, Xbarc133-3B, Xbarc147-3B and Xgwm493-3B {10073}.’

 

Qfhs.ifa-5A {10076}.  Associated mainly with resistance to fungal penetration {10073}.  5A {0240,10076}.  v:  Remus / CM-82036 {10076}.  ma: Associated with markers Xgwm293-5A, Xgwm304-5A, Xgwm1057-5A, Xbarc117-5A, Xbarc186-5A, Xbarc100-5A and Xbarc40-5A {10073}.

 

QTLs for resistance to Fusarium graminearum detected in the cross Renan/Recital {10069}. All resistance alleles, except QFhs.inra-3A, were contributed by Renan. LOD scores and percent of variation explained by the QTL (R2) are averages of three years of field tests.

QFhs.inra-2A {10069}.     

ma:

Associated with Xgwm382c-2A (LOD= 6.3, R2= 14.4%).

QFhs.inra-2B {10069}.     

ma:

Associated with Xgwm374-2B (LOD= 7.6, R2= 12%).

QFhs.inra-3A {10069}.     

ma:

Associated with Xbcd372-3A (LOD= 3.7, R2= 6.2%).

QFhs.inra-3B {10069}.     

ma:

Associated with Xgwm383b-3B (LOD= 5.4, R2=10.5% ).

QFhs.inra-5A.1 {10069}.  

ma:

Associated with Xpsr170a-5A (LOD= 3.8, R2= 5%).

QFhs.inra-5A.2{10069}.   

ma:

Associated with Xgwm639b-5A (LOD= 6.6, R2= 14%).