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向日葵属叶绿体DNA的变异性:DNA-DNA异源双链体的限制性分析和S1核酸酶图谱分析

Chloroplast DNA variability in the genus Helianthus: restriction analysis and S1 nuclease mapping of DNA-DNA heteroduplexes.

作者信息

Serror P, Heyraud F, Heizmann P

机构信息

Laboratoire de Biologie Cellulaire, Université Claude-Bernard, Lyon, France.

出版信息

Plant Mol Biol. 1990 Aug;15(2):269-80. doi: 10.1007/BF00036913.

Abstract

Chloroplast DNA (cpDNA) from 36 wild species of the genus Helianthus has been analysed with three restriction endonucleases (Bam HI, Hind III and Sst I). Out of the 71 restriction sites described on the reference cpDNA (sunflower cpDNA), three insertions/deletions and seven site modifications were detected during the survey of the other cpDNAs. Since restriction mapping showed only a very limited fraction of the DNA variability, we chose to adapt the S1 nuclease mapping technique to detect fine variations between chloroplast genomes. For this purpose, DNA-DNA heteroduplexes obtained between sunflower and wild-species DNAs were digested by S1 nuclease and the resulting mismatches were detected by classical endonuclease restriction and hybridization methods. The S1 nuclease mapping results were confirmed by sequencing one S1 nuclease-sensitive region detected between cultivated sunflower and two perennial wild-type species. As a result of these analyses, it appeared that the combination of restriction mapping and S1 nuclease mapping might be helpful to differentiate taxonomically close cytoplasms.

摘要

已用三种限制性内切酶(Bam HI、Hind III和Sst I)对36种野生向日葵属植物的叶绿体DNA(cpDNA)进行了分析。在参考cpDNA(向日葵cpDNA)上描述的71个限制性位点中,在对其他cpDNA的调查过程中检测到了三个插入/缺失和七个位点修饰。由于限制性图谱仅显示了DNA变异性的非常有限的部分,我们选择采用S1核酸酶图谱技术来检测叶绿体基因组之间的细微变异。为此,用S1核酸酶消化向日葵和野生种DNA之间获得的DNA-DNA异源双链体,并通过经典的内切酶限制性和杂交方法检测产生的错配。通过对栽培向日葵和两个多年生野生型物种之间检测到的一个S1核酸酶敏感区域进行测序,证实了S1核酸酶图谱结果。这些分析的结果表明,限制性图谱和S1核酸酶图谱的结合可能有助于区分分类学上相近的细胞质。

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