Werner J E, Endo T R, Gill B S
Department of Plant Pathology, Kansas State University, Manhattan 66506-5502.
Proc Natl Acad Sci U S A. 1992 Dec 1;89(23):11307-11. doi: 10.1073/pnas.89.23.11307.
Bread wheat (Triticum aestivum L. em Thell) is well suited for cytogenetic analysis because the genome, buffered by polyploidy, can tolerate structurally and numerically engineered chromosomes for analysis over infinite generations. This feature of polyploidy can be used in developing a high-resolution, cytogenetically based physical map of the wheat genome. We show that numerous deletions, observed in the progeny of a monosomic addition of a chromosome from Triticum cylindricum in wheat, result from single breakpoints and a concomitant loss of distal fragments. Breakages occurred in euchromatic and heterochromatic regions. Forty-one deletions for chromosomes 7A, 7B, and 7D, and a set of genetically mapped DNA probes, were used to construct physical maps. Recombination was low in proximal chromosomal regions and very high toward the distal ends. Deletion mapping was more efficient than genetic mapping in resolving the order of proximal loci. Despite variation in size and arm ratio, relative gene position was largely conserved among chromosomes 7A, 7B, and 7D and a consensus group 7 physical map was constructed. Several molecularly tagged chromosome regions (MTCRs) of approximately one to a few million base pairs were identified that may be resolved by long-range mapping of DNA fragments. Thus, a cytogenetically based physical map may be used to integrate chromosome and DNA-based maps. The MTCRs may simplify strategies for cloning of agronomically useful genes despite the genetic complexity and the large genome size of wheat.
面包小麦(Triticum aestivum L. em Thell)非常适合进行细胞遗传学分析,因为其基因组由多倍体缓冲,能够耐受经过结构和数量改造的染色体,以便在无数代中进行分析。多倍体的这一特性可用于构建基于细胞遗传学的小麦基因组高分辨率物理图谱。我们发现,在小麦中添加来自圆柱小麦的一条染色体的单体附加系后代中观察到的大量缺失,是由单个断点以及远端片段的伴随丢失导致的。断裂发生在常染色质和异染色质区域。利用7A、7B和7D染色体的41个缺失以及一组遗传定位的DNA探针构建了物理图谱。近端染色体区域的重组率较低,而远端的重组率非常高。在解析近端基因座的顺序方面,缺失作图比遗传作图更有效。尽管大小和臂比存在差异,但7A、7B和7D染色体之间的相对基因位置在很大程度上是保守的,并构建了一个第7组的共识物理图谱。鉴定出了几个大小约为100万至数百万碱基对的分子标记染色体区域(MTCR),这些区域可能通过DNA片段的长程作图来解析。因此,基于细胞遗传学的物理图谱可用于整合基于染色体和基于DNA的图谱。尽管小麦的遗传复杂性高且基因组大,但MTCR可能会简化克隆具有农艺价值基因的策略。