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磷酸丙糖异构酶叶绿体同工酶的遗传学与进化

Genetics and evolution of chloroplast isozymes of triosephosphate isomerase.

作者信息

Feierabend J, Kurzok H G, Schmidt M

机构信息

Botanisches Institut, J.W. Goethe-Universität, Frankfurt am Main, F.R.G.

出版信息

Prog Clin Biol Res. 1990;344:665-82.

PMID:2392479
Abstract

Triosephosphate isomerase is an ubiquitous and highly conservative dimeric enzyme, consisting of subunits of Mr 26,000-27,000. Plants usually contain one cytosolic and one plastid isozyme. While 2x wheats also contain one plastid isozyme, 4x wheats contain 3, and 6x cultural wheats contain five plastid isozymes. The multiplicity of the isozyme pattern in 6x wheats is explainable by the presence of three different genomes (AABBDD), each contributing a distinct triosephosphate isomerase gene (alpha',beta,delta), and by the formation of homodimeric and heterodimeric isozyme forms. While the beta beta-form was, as expected, also found in Aegilops speltoides which is regarded as donor of the B genome, the descent of the other genes for plastid triosephosphate isomerase did not occur in accordance with common contentions on the evolution of 6x cultural wheat and its presumptive ancestors. In the reciprocal intergeneric hybrids between wheat and rye, Secalotricum and Triticale, the patterns of both the cytosolic and the plastid-specific triosephosphate isomerases were biparentally inherited, indicating also that the plastid isozyme was nuclear-encoded. Data which are available about amino acid sequences and gene organization and immunological observations show that the cytosolic triosephosphate isomerase of plants is strongly related to other eukaryotic animal triosephosphate isomerase genes. Multiple evidence has been presented that the plastid- specific isozyme represents a distinct polypeptide and is specified by a distinct gene, relative to the cytosolic isozyme. Immunological comparisons indicate that the plastid isozyme shares homologies with the cytosolic isozyme but is not related to the enzyme from prokaryotic cyanobacteria or bacteria. To enable a more precise comparison, plastid triosephosphate isomerase has been cloned from a cDNA library from rye, and cDNA clones are being sequenced. The plastid enzyme of triosephosphate isomerase appears to have evolved from a duplication on an ancestral nuclear gene of the primordial plant cell. For other plastid-specific isozymes evidence exists that their genes were incorporated into the nucleus by gene transfer from a prokaryotic endosymbiont.

摘要

磷酸丙糖异构酶是一种普遍存在且高度保守的二聚体酶,由分子量为26,000 - 27,000的亚基组成。植物通常含有一种胞质异构酶和一种质体异构酶。二倍体小麦也含有一种质体异构酶,四倍体小麦含有3种,而六倍体栽培小麦含有5种质体异构酶。六倍体小麦中异构酶模式的多样性可以通过存在三种不同的基因组(AABBDD)来解释,每个基因组贡献一个独特的磷酸丙糖异构酶基因(α'、β、δ),并通过形成同二聚体和异二聚体异构酶形式来解释。正如预期的那样,在被视为B基因组供体的斯卑尔脱山羊草中也发现了ββ形式,而质体磷酸丙糖异构酶其他基因的起源并不符合关于六倍体栽培小麦及其假定祖先进化的普遍观点。在小麦与黑麦、黑小麦和小黑麦的正反交属间杂种中,胞质和质体特异性磷酸丙糖异构酶的模式都是双亲遗传的,这也表明质体异构酶是由核编码的。关于氨基酸序列、基因组织和免疫学观察的现有数据表明,植物的胞质磷酸丙糖异构酶与其他真核动物的磷酸丙糖异构酶基因密切相关。有多项证据表明,相对于胞质异构酶,质体特异性异构酶代表一种独特的多肽,并由一个独特的基因指定。免疫学比较表明,质体异构酶与胞质异构酶有同源性,但与原核蓝细菌或细菌的酶无关。为了进行更精确的比较,已从黑麦的cDNA文库中克隆了质体磷酸丙糖异构酶,并对cDNA克隆进行测序。磷酸丙糖异构酶的质体酶似乎是从原始植物细胞的一个祖先核基因的复制进化而来的。对于其他质体特异性异构酶,有证据表明它们的基因是通过从原核内共生体的基因转移而整合到细胞核中的。

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