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矮牵牛中与雄性不育相关的pcf基因和正常的atp9 - 1基因位于不同的线粒体DNA分子上。

The male sterility-associated pcf gene and the normal atp9-1 gene in Petunia are located on different mitochondrial DNA molecules.

作者信息

Folkerts O, Hanson M R

机构信息

Section of Genetics and Development, Cornell University, Ithaca, New York 14853.

出版信息

Genetics. 1991 Nov;129(3):885-95. doi: 10.1093/genetics/129.3.885.

Abstract

A mitochondrial DNA (mtDNA) region termed the S-pcf locus has previously been correlated with cytoplasmic male sterility (CMS) in Petunia. In order to understand the relationship of the S-pcf locus to homologous sequences found elsewhere in mtDNAs of both CMS and fertile lines, the structure of the mitochondrial genome of CMS Petunia line 3688 was determined by cosmid walking. The S-pcf locus, which includes the only copies of genes for NADH dehydrogenase subunit 3 (nad3) and small ribosomal subunit protein 12 (rps12) was found to be located on a circular map of 396 kb, while a second almost identical circular map of 407 kb carries the only copies of the genes for 18S and 5S rRNA (rrn18 and rrn5), the only copy of a conserved unidentified gene (orf25), and the only known functional copy of atp9. Three different copies of a recombination repeat were found in six genomic environments, predicting sub-genomic circles of 277, 266 and 130 kb. The ratio of atp9 to S-pcf mtDNA sequences was approximately 1.5 to 1, indicating that sub-genomic molecules carrying these genes differ in abundance. Comparison of the mtDNA organization of the CMS line with that of the master circle of fertile Petunia line 3704 reveals numerous changes in order and orientation of ten different sectors.

摘要

一个被称为S-pcf位点的线粒体DNA(mtDNA)区域先前已被证明与矮牵牛的细胞质雄性不育(CMS)相关。为了了解S-pcf位点与CMS系和可育系mtDNA中其他地方发现的同源序列之间的关系,通过黏粒步移法确定了CMS矮牵牛系3688线粒体基因组的结构。发现包含NADH脱氢酶亚基3(nad3)和小核糖体亚基蛋白12(rps12)基因唯一拷贝的S-pcf位点位于一个396 kb的环状图谱上,而另一个407 kb的几乎相同的环状图谱携带18S和5S rRNA(rrn18和rrn5)基因的唯一拷贝、一个保守的未鉴定基因(orf25)的唯一拷贝以及atp9的唯一已知功能拷贝。在六个基因组环境中发现了重组重复的三个不同拷贝,预测有277、266和130 kb的亚基因组环。atp9与S-pcf mtDNA序列的比例约为1.5比1,表明携带这些基因的亚基因组分子在丰度上有所不同。将CMS系的mtDNA组织与可育矮牵牛系3704的主环进行比较,发现十个不同区段的顺序和方向有许多变化。

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