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高等植物叶绿体和胞质中的3-磷酸甘油酸激酶:内共生基因替代的一个实例。

Higher-plant chloroplast and cytosolic 3-phosphoglycerate kinases: a case of endosymbiotic gene replacement.

作者信息

Brinkmann H, Martin W

机构信息

Institut für Botanik, Technische Universität Braunschweig, Germany.

出版信息

Plant Mol Biol. 1996 Jan;30(1):65-75. doi: 10.1007/BF00017803.

Abstract

Previous studies indicated that plant nuclear genes for chloroplast and cytosolic isoenzymes of 3-phosphoglycerate kinase (PGK) arose through recombination between a preexisting gene of the eukaryotic host nucleus for the cytosolic enzyme and an endosymbiont-derived gene for the chloroplast enzyme. We readdressed the evolution of eukaryotic pgk genes through isolation and characterisation of a pgk gene from the extreme halophilic, photosynthetic archaebacterium Haloarcula vallismortis and analysis of PGK sequences from the three urkingdoms. A very high calculated net negative charge of 63 for PGK from H. vallismortis was found which is suggested to result from selection for enzyme solubility in this extremely halophilic cytosol. We refute the recombination hypothesis proposed for the origin of plant PGK isoenzymes. The data indicate that the ancestral gene from which contemporary homologues for the Calvin cycle/glycolytic isoenzymes in higher plants derive was acquired by the nucleus from (endosymbiotic) eubacteria. Gene duplication subsequent to separation of Chlamydomonas and land plant lineages gave rise to the contemporary genes for chloroplast and cytosolic PGK isoenzymes in higher plants, and resulted in replacement of the preexisting gene for PGK of the eukaryotic cytosol. Evidence suggesting a eubacterial origin of plant genes for PGK via endosymbiotic gene replacement indicates that plant nuclear genomes are more highly chimaeric, i.e. contain more genes of eubacterial origin, than is generally assumed.

摘要

先前的研究表明,叶绿体和胞质3-磷酸甘油酸激酶(PGK)同工酶的植物核基因是通过真核宿主细胞核中胞质酶的一个预先存在的基因与叶绿体酶的一个内共生体衍生基因之间的重组产生的。我们通过从极端嗜盐光合古细菌死谷嗜盐菌中分离和鉴定一个pgk基因,并分析三个超界的PGK序列,重新探讨了真核pgk基因的进化。我们发现死谷嗜盐菌的PGK计算出的净负电荷非常高,为63,这被认为是由于在这种极端嗜盐的细胞质中选择酶的溶解性所致。我们反驳了为植物PGK同工酶起源提出的重组假说。数据表明,高等植物卡尔文循环/糖酵解同工酶的当代同源物所源自的祖先基因是细胞核从(内共生)真细菌获得的。衣藻和陆地植物谱系分离后的基因复制产生了高等植物中叶绿体和胞质PGK同工酶的当代基因,并导致真核细胞质中预先存在的PGK基因被取代。通过内共生基因替代表明植物PGK基因起源于真细菌的证据表明,植物核基因组比一般认为的更具嵌合性,即包含更多源自真细菌的基因。

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