Genetic mapping of the gene for brittle rachis in a Triticum aestivum—Aegilops triuncialis introgression line

2011 ◽  
Vol 59 (1) ◽  
pp. 67-72 ◽  
Author(s):  
K. Yoshiya ◽  
N. Watanabe ◽  
T. Kuboyama ◽  
I. F. Lapochkina
1980 ◽  
Vol 22 (2) ◽  
pp. 197-212
Author(s):  
S. S. Maan

The Triticum aestivum L. (2n = 42; AABBDD) and T. durum Desf. (2n = 28; AABB) genomes were substituted into the cytoplasm of two Aegilops triuncialis L. (2n = 28; CCCuCu) accessions. In F1 (ABCCu) and in a 42-chromosome backcross plant (AABBCCu) meiotic pairing between the C- and Cu-genome chromosomes was substantially reduced. Therefore, some of the pairing in the F1 of Ae. caudata L. (2n = 14; CC) × Ae. umbellulata Zhuk. (2n = 14; CuCu) may have been of the homoelogous type. In early backcrosses with T. aestivum, the euploid gametes or zygotes did not function in plants having Aegilops chromosome(s), but euploid plants with Ae. triuncialis cytoplasm were obtained in the fifth backcross. These plants were used as the cytoplasmic source to substitute the T. durum genomes into Ae. triuncialis cytoplasm; euploid durum plants were obtained in the second backcross. Alloplasmic T. durum and T. aestivum plants with Ae. triuncialis cytoplasm had closer resemblance to the plants with Ae. umbellulata cytoplasm than to those with Ae. caudata cytoplasm. These nucleo-cytoplasmic interactions indicated cytoplasmic similarity between Ae. umbellulata and Ae. triuncialis.


2011 ◽  
Vol 41 (No. 2) ◽  
pp. 39-44 ◽  
Author(s):  
N. Watanabe ◽  
N. Takesada ◽  
Y. Fujii ◽  
P. Martinek

The brittle rachis phenotype is of adaptive value in wild grass species because it causes spontaneous spike shattering. The genes on the homoeologous group 3 chromosomes determine the brittle rachis in Triticeae. A few genotypes with brittle rachis have also been found in the cultivated Triticum. Using microsatellite markers, the homoeologous genes for brittle rachis were mapped in hexaploid wheat (Triticum aestivum L.), durum wheat (Triticum turgidum L. conv. durum /Desf./) and Aegilops tauschii Coss. On chromosome 3AS, the gene for brittle rachis, Br<sub>2</sub>, was linked with the centromeric marker, Xgwm32, at the distance of 13.3 cM. Br<sub>3 </sub>was located on chromosome 3BS and linked with the centromeric marker,<br />Xgwm72 (14.2 cM). Br<sub>1 </sub>was located on chromosome 3DS. The distance from the centromeric marker Xgdm72 was 23.6 cM. The loci Br<sub>1</sub>, Br<sub>2</sub> and Br<sub>3</sub> determine disarticulation of rachides above the junction of the rachilla with the rachis so that a fragment of rachis is attached below each spikelet. The rachides of Ae. tauschii are brittle at every joint, so that the mature spike disarticulates into barrel type. The brittle rachis was determined by a dominant gene, Br<sup>t</sup>, which was linked to the centromeric marker, Xgdm72 (19.7 cM), on chromosome 3DS. A D-genome introgression line, R-61, was derived from the cross Bet Hashita/Ae. tauschii, whose rachis disarticulated as a wedge type. The gene for brittle rachis of R-61, tentatively designated as Br<sup>61</sup>, was distally located on chromosome 3DS, and was linked with the centromeric marker, Xgdm72 (27.5 cM). We discussed how the brittle rachis of R-61 originated genetically. &nbsp; &nbsp;


2016 ◽  
Vol 129 (6) ◽  
pp. 1127-1137 ◽  
Author(s):  
I. N. Bheema Lingeswara Reddy ◽  
K. Chandrasekhar ◽  
Y. Zewdu ◽  
A. Dinoor ◽  
B. Keller ◽  
...  

2006 ◽  
Vol 113 (7) ◽  
pp. 1271-1281 ◽  
Author(s):  
M. J. Hayden ◽  
P. Stephenson ◽  
A. M. Logojan ◽  
D. Khatkar ◽  
C. Rogers ◽  
...  

Genome ◽  
2004 ◽  
Vol 47 (6) ◽  
pp. 1130-1136 ◽  
Author(s):  
Xiu-Qiang Huang ◽  
Sai L.K Hsam ◽  
Volker Mohler ◽  
Marion S Röder ◽  
Friedrich J Zeller

A set of differential isolates of Blumeria graminis f.sp. tritici was used to identify 10 alleles at the Pm3 locus on the short arm of chromosome 1A. Three F3 populations were used to map Pm3h in Abessi, Pm3i in line N324, and Pm3j alleles in GUS 122 relative to microsatellite markers. In total, 13 marker loci were mapped on chromosome 1AS and 1 marker on 1AL. The order of marker loci in the 3 mapping populations is consistent with previously published maps. All 3 alleles were mapped in the distal region of chromosome 1AS. The present study indicated that microsatellite markers are an ideal marker system for comparative mapping of alleles at the same gene locus in different mapping populations. The linkage distances of the closest microsatellite marker, Xgwm905–1A, to Pm3h, Pm3i, and Pm3j were 3.7 cM, 7.2 cM, and 1.2 cM, respectively. The microsatellite marker Xgwm905–1A cannot be used to distinguish between Pm3 alleles. The development of specific markers for individual Pm3 alleles is discussed on the basis of the recently cloned Pm3b allele.Key words: genetic mapping, marker-assisted selection, microsatellite markers, Pm3 locus, powdery mildew resistance, Triticum aestivum.


2008 ◽  
Vol 22 (4) ◽  
pp. 675-685 ◽  
Author(s):  
Fanguo Chen ◽  
Chunhui Xu ◽  
Mengzhu Chen ◽  
Yanhui Wang ◽  
Guangmin Xia

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