Luo Qiaoling, Zheng Qi, Tong Chunyan, Jia Hongwei, Liu Liqin, Yin Mou, Xie Jingzhong, Li Hongwei, Wang Hongxin, Chen Zeyang, Li Bin, He Fei, Li Zhensheng
State Key Laboratory of Plant Cell and Chromosome Engineering, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, 100101, China.
University of Chinese Academy of Sciences, Beijing, 100049, China.
Theor Appl Genet. 2025 Feb 1;138(2):41. doi: 10.1007/s00122-025-04826-x.
The location of alien chromatin in Xiaoyan 6 was identified using mc-GISH analysis, genetic mapping and whole genome re-sequencing, and its possible origin was discussed. As a founder parent, Xiaoyan 6 has played an important role in distant hybridization breeding in China. Although it came from the cross between common wheat and Thinopyrum ponticum (Podp.) Barkworth and D.R. Dewey, the location of its alien chromatin has not been determined using traditional genomic in situ hybridization (GISH). In the present study, chromosome variation in Xiaoyan 6 was discovered by multicolor GISH analysis. Four alien-specific markers were developed by specific-locus amplified fragment sequencing technique. Their amplified sequences were analyzed by basic local alignment search tool with the reference genome sequences of common wheat Chinese Spring (CS) and Th. elongatum, and the whole genome re-sequencing reads of Th. ponticum and CS. Furthermore, the four markers were mapped on three different chromosomes in two RIL populations. By dissecting the mapped reads depth of the whole genome re-sequencing of Xiaoyan 6, we found that the depth of nine chromosome regions was obviously lower than the average. Among these, three regions on 1A, 3A and 7B were demonstrated as the alien introgressions in Xiaoyan 6 by multiple methods. Finally, the genetic transmission of the alien chromatin was analyzed in a set of wheat-Th. ponticum introgression lines. Some stable QTLs for morphological and physiological traits have been mapped near the alien chromatin.
利用甲基化敏感基因组原位杂交(mc-GISH)分析、遗传作图和全基因组重测序确定了小偃6号中外源染色质的位置,并讨论了其可能的起源。作为一个骨干亲本,小偃6号在中国远缘杂交育种中发挥了重要作用。尽管它来自普通小麦与长穗偃麦草(Podp.)Barkworth和D.R. Dewey的杂交,但利用传统的基因组原位杂交(GISH)尚未确定其外源染色质的位置。在本研究中,通过多色GISH分析发现了小偃6号的染色体变异。利用特异位点扩增片段测序技术开发了4个外源特异标记。通过基本局部比对搜索工具,将其扩增序列与普通小麦中国春(CS)和长穗偃麦草的参考基因组序列以及长穗偃麦草和CS的全基因组重测序reads进行分析。此外,将这4个标记定位在两个重组自交系群体的3条不同染色体上。通过剖析小偃6号全基因组重测序的定位reads深度,发现9个染色体区域的深度明显低于平均值。其中,通过多种方法证明1A、3A和7B上的3个区域是小偃6号中的外源渐渗区域。最后,在一组小麦-长穗偃麦草渐渗系中分析了外源染色质的遗传传递。在靠近外源染色质的区域定位了一些形态和生理性状的稳定QTL。