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诱变剂诱导的T型细胞质玉米rf1核育性恢复基因的突变改变了T-urf13线粒体转录本的积累。

Mutator-induced mutations of the rf1 nuclear fertility restorer of T-cytoplasm maize alter the accumulation of T-urf13 mitochondrial transcripts.

作者信息

Wise R P, Dill C L, Schnable P S

机构信息

USDA-Agricultural Research Service, Iowa State University, Ames 50011, USA.

出版信息

Genetics. 1996 Jul;143(3):1383-94. doi: 10.1093/genetics/143.3.1383.

DOI:10.1093/genetics/143.3.1383
PMID:8807309
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1207406/
Abstract

Dominant alleles of the rf1 and rf2 nuclear-encoded fertility restorer genes are necessary for restoration of pollen fertility in T-cytoplasm maize. To further characterize fertility restoration mediated by the Rf1 allele, 123,500 gametes derived from plants carrying the Mutator transposable element family were screened for rf1-mutant alleles (rf1-m) Four heritable rf1-m alleles were recovered from these populations. Three rf1-m alleles were derived from the progenitor allele Rf1-IA153 and one was derived from Rf1-Ky21. Cosegregation analysis revealed 5.5- and 2.4-kb Mu1-hybridizing EcoRI restriction fragments in all of the male-sterile and none of the male-fertile plants in families segregating for rf1-m3207 and rf1-m3310, respectively. Mitochondrial RNA gel blot analyses indicated that all four rf1-m alleles in male-sterile plants cosegregated with the altered steady-state accumulation of 1.6- and 0.6-kb T-urf13 transcripts, demonstrating that these transcripts are Rf1 dependent. Plants carrying a leaky mutant, rf1-m7323, revealed variable levels of Rf1-associated, T-urf13 transcripts and the degree of pollen fertility. The ability to obtain rf1-m derivatives from Rf1 indicates that Rf1 alleles produce a functional gene product necessary for the accumulation of specific T-urf13 transcripts in T-cytoplasm maize.

摘要

rf1和rf2这两个核编码育性恢复基因的显性等位基因是恢复T型细胞质玉米花粉育性所必需的。为了进一步表征由Rf1等位基因介导的育性恢复,对携带Mutator转座子家族的植物产生的123,500个配子进行了rf1突变等位基因(rf1-m)筛选。从这些群体中获得了四个可遗传的rf1-m等位基因。三个rf1-m等位基因源自祖先等位基因Rf1-IA153,一个源自Rf1-Ky21。共分离分析显示,在分别针对rf1-m3207和rf1-m3310进行分离的家系中,所有雄性不育植株均有5.5 kb和2.4 kb的Mu1杂交EcoRI限制性片段,而所有雄性可育植株均无此片段。线粒体RNA凝胶印迹分析表明,雄性不育植株中的所有四个rf1-m等位基因均与1.6 kb和0.6 kb的T-urf13转录本稳态积累的改变共分离,表明这些转录本依赖于Rf1。携带渗漏突变体rf1-m7323的植株显示出不同水平的与Rf1相关的T-urf13转录本以及花粉育性程度。从Rf1获得rf1-m衍生物的能力表明,Rf1等位基因产生了T型细胞质玉米中特定T-urf13转录本积累所必需的功能性基因产物。

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