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由基因座重复和缺失导致的小麦同源染色体间的共线性扰动与重组率相关。

Synteny perturbations between wheat homoeologous chromosomes caused by locus duplications and deletions correlate with recombination rates.

作者信息

Akhunov Eduard D, Akhunova Alina R, Linkiewicz Anna M, Dubcovsky Jorge, Hummel David, Lazo Gerry, Chao Shiaoman, Anderson Olin D, David Jacques, Qi Lili, Echalier Benjamin, Gill Bikram S, Gustafson J Perry, La Rota Mauricio, Sorrells Mark E, Zhang Deshui, Nguyen Henry T, Kalavacharla Venugopal, Hossain Khwaja, Kianian Shahryar F, Peng Junhua, Lapitan Nora L V, Wennerlind Emily J, Nduati Vivienne, Anderson James A, Sidhu Deepak, Gill Kulvinder S, McGuire Patrick E, Qualset Calvin O, Dvorak Jan

机构信息

Department of Agronomy and Range Science, University of California, Davis, CA 95616, USA.

出版信息

Proc Natl Acad Sci U S A. 2003 Sep 16;100(19):10836-41. doi: 10.1073/pnas.1934431100. Epub 2003 Sep 5.

DOI:10.1073/pnas.1934431100
PMID:12960374
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC196889/
Abstract

Loci detected by Southern blot hybridization of 3,977 expressed sequence tag unigenes were mapped into 159 chromosome bins delineated by breakpoints of a series of overlapping deletions. These data were used to assess synteny levels along homoeologous chromosomes of the wheat A, B, and D genomes, in relation to both bin position on the centromere-telomere axis and the gradient of recombination rates along chromosome arms. Synteny level decreased with the distance of a chromosome region from the centromere. It also decreased with an increase in recombination rates along the average chromosome arm. There were twice as many unique loci in the B genome than in the A and D genomes, and synteny levels between the B genome chromosomes and the A and D genome homoeologues were lower than those between the A and D genome homoeologues. These differences among the wheat genomes were attributed to differences in the mating systems of wheat diploid ancestors. Synteny perturbations were characterized in 31 paralogous sets of loci with perturbed synteny. Both insertions and deletions of loci were detected and both preferentially occurred in high recombination regions of chromosomes.

摘要

通过对3977个表达序列标签单基因进行Southern杂交检测到的基因座,被定位到由一系列重叠缺失的断点所界定的159个染色体区间中。这些数据用于评估小麦A、B和D基因组同源染色体上的同线性水平,这与着丝粒 - 端粒轴上的区间位置以及染色体臂上重组率的梯度有关。同线性水平随着染色体区域与着丝粒距离的增加而降低。它也随着沿平均染色体臂重组率的增加而降低。B基因组中的独特基因座数量是A和D基因组中的两倍,并且B基因组染色体与A和D基因组同源染色体之间的同线性水平低于A和D基因组同源染色体之间的同线性水平。小麦基因组之间的这些差异归因于小麦二倍体祖先交配系统的差异。在31组具有同线性扰动的旁系同源基因座中对同线性扰动进行了表征。检测到基因座的插入和缺失,并且两者都优先发生在染色体的高重组区域。

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