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悬浮细胞、愈伤组织培养和再生诱导的甜菜线粒体 DNA 重排。

Rearrangements in sugar beet mitochondrial DNA induced by cell suspension, callus cultures and regeneration.

机构信息

Institute of Cytology and Genetics, Academy of Sciences of the USSR, Siberian Department, 630090, Novosibirsk, USSR.

出版信息

Theor Appl Genet. 1993 Jul;86(6):699-704. doi: 10.1007/BF00222659.

Abstract

Structural alterations in mitochondrial DNAs (mtDNAs) from a plant of a sterile sugar beet line, callus derived from it, suspension-cultured cells and plants regenerated from the callus were studied. BamHI restriction analysis revealed that structural alterations between the mtDNAs of the callus and the control plant had occurred. Multiple rearrangements were also demonstrated in the mtDNA from the suspension culture, of which some were similar to those appearing in the callus, and others had arisen de novo. Rearrangements were also identified by means of blot hybridization of BamHI-digested mtDNA from suspension-cultured cells with the genes encoding subunit II of cytochrome oxidase (cox II) and subunit 1 of NADH-dehydrogenase (Nd1). No alterations were observed in the mitochondrial genome of the callus and regenerants. The location of the genes for the α-subunit of F1-ATPase (atpA) and apocytochrome b (cob) in the mtDNA remained unchanged.Our salient finding was of a plant with an altered mitochondrial genome as judged by EcoRI and BamHI restriction analysis. This exceptional plant had retained the sterile phenotype like all of the other regenerants and the parent. The set of plasmid-like molecules of mtDNA remained the same as that in the control plant and in all of the regenerants, callus and suspension-cultured cells. The only type of plasmid-like molecule found in all of the DNAs was the 1.6-kbp minicircle, which is a feature of sterile cytoplasms. These structural changes in mtDNA were obviously a consequence of somaclonal variation during the in vitro cultivation of the sugar beet cells.

摘要

对不育甜菜品系的植株、其愈伤组织、悬浮培养细胞以及由愈伤组织再生的植株的线粒体 DNA(mtDNA)的结构改变进行了研究。BamHI 限制分析显示,愈伤组织与对照植株的 mtDNA 之间发生了结构改变。悬浮培养的 mtDNA 还显示出多种重排,其中一些与愈伤组织中的相似,而另一些则是新出现的。通过用 BamHI 消化的悬浮培养细胞的 mtDNA 与编码细胞色素氧化酶亚基 II(cox II)和 NADH 脱氢酶亚基 1(Nd1)的基因进行斑点杂交,也鉴定出了重排。在愈伤组织和再生体的线粒体基因组中未观察到改变。F1-ATP 酶(atpA)的α亚基和细胞色素 b(cob)基因在 mtDNA 中的位置没有改变。我们的主要发现是,通过 EcoRI 和 BamHI 限制分析判断,一种线粒体基因组发生改变的植物。这种特殊的植物保留了与其他再生体和亲本相同的不育表型。mtDNA 的质粒样分子集合与对照植物和所有再生体、愈伤组织和悬浮培养细胞中的相同。在所有 DNA 中发现的唯一类型的质粒样分子是 1.6-kbp 的小型环,这是不育细胞质的特征。这些 mtDNA 的结构变化显然是甜菜细胞体外培养过程中体细胞变异的结果。

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