Pan Zijin, Luo Jie, Tang Zongxiang, Fu Shulan
College of Agronomy, Sichuan Agricultural University, Wenjiang, Chengdu 611130, China.
Provincial Key Laboratory for Plant Genetics and Breeding, Sichuan Agricultural University, Wenjiang, Chengdu 611130, China.
Plants (Basel). 2022 Aug 15;11(16):2117. doi: 10.3390/plants11162117.
Single-copy FISH analysis is a useful tool to physically locate a given sequence on chromosome. Centromeric single-copy sequences can be used to locate the position of centromere and disclose the subtle differences among different centromeres. Nine centromeric single-copy sequences 1R1, 3R1, 4R1, 4R2, 5R1, 5R2, 6R2, 6R3, and 7R1 were cloned from Kustro ( L.). FISH analysis using these sequences as probes indicated that the signals of 1R1, 3R1, 4R1, 4R2, 5R1, 5R2, 6R1, 6R2, and 7R1 were located in the centromeric regions of rye 1R, 3R, 4R, 4R, 5R, 5R, 6R, 6R, and 7R chromosomes, respectively. In addition, for each of the centromeric single-copy sequences, high sequence similarity was observed among different species. Combined with rye genomic sequence, single-copy FISH analysis indicated that the 1BL.1RS translocations in wheat cultivar CN17 and wheat line 20T363-4 contained the centromeric segment of 1R chromosome from 349,498,361 to 349,501,266 bp, and the 1BL.1RS translocations in the other two wheat cultivars did not contain this segment. The nine sequences are useful in determining the centromere location on rye chromosomes, and they have the potential to disclose the accurate structural differences of centromeres among the wheat-rye centric fusion translocation chromosomes; therefore, more centromeric single-copy sequences are needed.
单拷贝荧光原位杂交(FISH)分析是在染色体上物理定位特定序列的有用工具。着丝粒单拷贝序列可用于定位着丝粒的位置,并揭示不同着丝粒之间的细微差异。从黑麦(L.)品种Kustro中克隆了9个着丝粒单拷贝序列1R1、3R1、4R1、4R2、5R1、5R2、6R2、6R3和7R1。以这些序列为探针进行FISH分析表明,1R1、3R1、4R1、4R2、5R1、5R2、6R1、6R2和7R1的信号分别位于黑麦1R、3R、4R、4R、5R、5R、6R、6R和7R染色体的着丝粒区域。此外,对于每个着丝粒单拷贝序列,在不同物种间观察到高度的序列相似性。结合黑麦基因组序列,单拷贝FISH分析表明,小麦品种CN17和小麦品系20T363 - 4中的1BL.1RS易位包含1R染色体349,498,361至349,501,266 bp的着丝粒区段,而其他两个小麦品种中的1BL.1RS易位不包含该区段。这九个序列有助于确定黑麦染色体上的着丝粒位置,并且有潜力揭示小麦 - 黑麦着丝粒融合易位染色体之间着丝粒的准确结构差异;因此,需要更多的着丝粒单拷贝序列。