Kanazawa A, Tozuka A, Shimamoto Y
Laboratory of Plant Genetics and Evolution, Faculty of Agriculture, Hokkaido University, Sapporo, Japan.
Genes Genet Syst. 1998 Apr;73(2):111-9. doi: 10.1266/ggs.73.111.
Restriction fragment length polymorphisms (RFLPs) of EcoRI-and ClaI-digested chloroplast DNA (cpDNA) within the genus Glycine subgenus Soja were characterized. Two mutations were found to be responsible for the EcoRI and ClaI restriction site polymorphisms, and both were located in a region in which many ribosomal protein genes are clustered. This region is within the large single copy region of cpDNA and is located close to an inverted repeat. The locations of restriction sites of EcoRI and ClaI in the cpDNA region were analyzed by DNA gel-blot analyses and PCR amplification, which were followed by sequencing analyses. The EcoRI site polymorphism was found to have occurred in the intergenic spacer between rps11 and rpl36, while the ClaI site polymorphism was located within the 3' part of the coding region of rps3. The mutations that cause EcoRI and ClaI polymorphisms were both found to be single base substitutions. In addition to these polymorphisms, novel sequence variations in soybean cpDNA were detected near the sites of these mutations. Previously, it was shown that cultivated soybeans could be classified into three groups (I, II, and III) based on their cpDNA RFLPs. A comparison of the cpDNA sequences of soybeans in the present study was consistent with the notion that the cpDNA of group II soybeans is an intermediate between the cpDNAs of groups I and II.
对大豆属(Glycine)大豆亚属(Soja)内用EcoRI和ClaI消化的叶绿体DNA(cpDNA)的限制性片段长度多态性(RFLP)进行了表征。发现两个突变导致了EcoRI和ClaI限制性位点多态性,且二者均位于许多核糖体蛋白基因成簇的区域。该区域位于cpDNA的大单拷贝区域内,且靠近一个反向重复序列。通过DNA凝胶印迹分析和PCR扩增对cpDNA区域中EcoRI和ClaI限制性位点的位置进行了分析,随后进行了测序分析。发现EcoRI位点多态性发生在rps11和rpl36之间的基因间隔区,而ClaI位点多态性位于rps3编码区的3'部分内。导致EcoRI和ClaI多态性的突变均为单碱基替换。除了这些多态性外,在这些突变位点附近还检测到了大豆cpDNA中的新序列变异。此前研究表明,栽培大豆可根据其cpDNA RFLP分为三组(I、II和III)。本研究中大豆cpDNA序列的比较与II组大豆的cpDNA是I组和III组cpDNA之间的中间类型这一观点一致。