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一个定位在Ph1亚显微缺失区域内的DNA片段,Ph1是多倍体小麦中的一个染色体配对调控基因。

A DNA fragment mapped within the submicroscopic deletion of Ph1, a chromosome pairing regulator gene in polyploid wheat.

作者信息

Gill K S, Gill B S

机构信息

Department of Plant Pathology, Kansas State University, Manhattan 66506-5502.

出版信息

Genetics. 1991 Sep;129(1):257-9. doi: 10.1093/genetics/129.1.257.

Abstract

Bread wheat is an allohexaploid consisting of three genetically related (homoeologous) genomes. The homoeologous chromosomes are capable of pairing but strict homologous pairing is observed at metaphase 1. The diploid-like pairing is regulated predominantly by Ph1, a gene mapped on long arm of chromosome 5B. We report direct evidence that a mutant of the gene (ph1b) arose from a submicroscopic deletion. A probe (XksuS1-5) detects the same missing fragment in two independent mutants ph1b and ph1c and a higher intensity fragment in a duplication of the Ph1 gene. It is likely that XksuS1-5 lies adjacent to Ph1 on the same chromosome fragment that is deleted in ph1b and ph1c. XksuS1-5 can be used to tag Ph1 gene to facilitate incorporation of genetic material from homoeologous genomes of the Triticeae. It may also be a useful marker in cloning Ph1 gene by chromosome walking.

摘要

普通小麦是一种异源六倍体,由三个基因相关(同源)的基因组组成。同源染色体能够配对,但在中期Ⅰ观察到严格的同源配对。类二倍体配对主要受位于5B染色体长臂上的Ph1基因调控。我们报告了该基因的一个突变体(ph1b)源自亚显微缺失的直接证据。一个探针(XksuS1-5)在两个独立的突变体ph1b和ph1c中检测到相同的缺失片段,在Ph1基因的一个重复中检测到一个强度更高的片段。XksuS1-5很可能位于与Ph1相同的染色体片段上,该片段在ph1b和ph1c中缺失。XksuS1-5可用于标记Ph1基因,以促进来自小麦族同源基因组的遗传物质的整合。它也可能是通过染色体步移克隆Ph1基因的一个有用标记。

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