期刊文献+

Genetic analysis and molecular mapping of a presenescing leaf gene psll in rice (Oryza sativa L.) 被引量:16

Genetic analysis and molecular mapping of a presenescing leaf gene psl1 in rice (Oryza sativa L.)
原文传递
导出
摘要 A rice psl1 (presenescing leaf) mutant was obtained from a japonica variety Zhonghua 11 via radiation of 60Co-γ in M2 generation. Every leaf of the mutant began to wither after it reached the big-gest length,while the leaves of the wild variety could keep green for 25―35 d. In this study,genetic analysis and gene mapping were carried out for the mutant identified. The SSR marker analysis showed that the mutant was controlled by a single recessive gene (psl1) located on chromosome 2. Fine mapping of the psl1 locus was conducted with 34 new STS markers developed around psl1 anchored region based on the sequence diversity between Nippon-bare and 93-11. The psl1 was further mapped be-tween two STS markers,STS2-19 and STS2-26,with genetic distances of 0.43 and 0.11 cM,respectively,while cosegregated with STS2-25. A BAC contig was found to span the psl1 locus,the region being delim-ited to 48 kb. This result was very useful for cloning of the psl1 gene. A rice psl1 (presenescing leaf) mutant was obtained from a japonica variety Zhonghua 11 via radiation of ^60Co-γ in M2 generation. Every leaf of the mutant began to wither after it reached the biggest length, while the leaves of the wild variety could keep green for 25--35 d. In this study, genetic analysis and gene mapping were carried out for the mutant identified. The SSR marker analysis showed that the mutant was controlled by a single recessive gene (psl1) located on chromosome 2. Fine mapping of the psl1 locus was conducted with 34 new STS markers developed around psl1 anchored region based on the sequence diversity between Nipponbare and 93-11. The psl1 was further mapped between two STS markers, STS2-19 and STS2-26, with genetic distances of 0.43 and 0.11 cM, respectively, while cosegregated with STS2-25. A BAC contig was found to span the psl1 locus, the region being delimited to 48 kb. This result was very useful for cloning of the psl1 gene.
出处 《Chinese Science Bulletin》 SCIE EI CAS 2006年第24期2986-2992,共7页
基金 Acknowledgements This work was supported by the State Key Program of Basic Research of China (Grant No. 30530118) the National Natural Science Foundation of China (Grant Nos. 2003CB114303 & 2005CB120807), and the Key Program of the Bureau of Education, Jiangsu, China (Grant No. 05KAJ2012).
关键词 psIl基因 水稻 叶片早衰 遗传分析 分子图谱 rice, simple sequence repeat (SSR) marker, sequencetagged site (STS) marker, molecular mapping, BAC contlg.
  • 相关文献

同被引文献73

引证文献16

二级引证文献73

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部