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黄色粘球菌发育过程中的基因表达。蛋白质S相关基因的分析。

Gene expression during development of Myxococcus xanthus. Analysis of the genes for protein S.

作者信息

Downard J S, Kupfer D, Zusman D R

出版信息

J Mol Biol. 1984 Jun 5;175(4):469-92. doi: 10.1016/0022-2836(84)90180-3.

Abstract

Protein S is an abundant spore coat protein produced during fruiting body formation (development) of the bacterium Myxococcus xanthus. We have cloned the DNA which codes for protein S and have found that this DNA hybridizes to three protein S RNA species from developmental cells but does not hybridize to RNA from vegetative cells. The half-life of protein S RNA was found to be unusually long, about 38 minutes, which, at least in part, accounts for the high level of protein S synthesis observed during development. Hybridization of restriction fragments from cloned M. xanthus DNA to the developmental RNAs enabled us to show that M. xanthus has two directly repeated genes for protein S (gene 1 and gene 2) which are separated by about 10(3) base-pairs on the bacterial chromosome. To study the expression of the protein S genes in M. xanthus, eight M. xanthus strains were isolated with Tn5 insertions at various positions in the DNA which codes for protein S. The strains which contained insertions in gene 1 or between gene 1 and gene 2 synthesized all three protein S RNA species and exhibited normal levels of protein S on spores. In contrast, M. xanthus strains exhibited normal levels of protein S on spores. In contrast, M. xanthus strains with insertions in gene 2 had no detectable protein S on spores and lacked protein S RNA. Thus, gene 2 is responsible for most if not all of the production of protein S during M. xanthus development. M. xanthus strains containing insertions in gene 1, gene 2 or both genes, were found to aggregate and sporulate normally even though strains bearing insertions in gene 2 contained no detectable protein S. We examined the expression of gene 1 in more detail by constructing a fusion between the lacZ gene of Escherichia coli and the N-terminal portion of protein S gene 1 of M. xanthus. The expression of beta-galactosidase activity in an M. xanthus strain containing the gene fusion was shown to be under developmental control. This result suggests that gene 1 is also expressed during development although apparently at a much lower level than gene 2.

摘要

蛋白质S是一种在黄色粘球菌子实体形成(发育)过程中产生的丰富的孢子外壳蛋白。我们已经克隆了编码蛋白质S的DNA,并发现该DNA与发育细胞中的三种蛋白质S RNA物种杂交,但不与营养细胞的RNA杂交。蛋白质S RNA的半衰期异常长,约为38分钟,这至少部分解释了在发育过程中观察到的蛋白质S的高水平合成。将克隆的黄色粘球菌DNA的限制性片段与发育RNA杂交,使我们能够证明黄色粘球菌有两个直接重复的蛋白质S基因(基因1和基因2),它们在细菌染色体上相隔约10³个碱基对。为了研究黄色粘球菌中蛋白质S基因的表达,分离了八个在编码蛋白质S的DNA的不同位置有Tn5插入的黄色粘球菌菌株。在基因1中或基因1与基因2之间含有插入的菌株合成了所有三种蛋白质S RNA物种,并在孢子上表现出正常水平的蛋白质S。相比之下,黄色粘球菌菌株在孢子上表现出正常水平的蛋白质S。相比之下,在基因2中含有插入的黄色粘球菌菌株在孢子上没有可检测到的蛋白质S,并且缺乏蛋白质S RNA。因此,基因2负责黄色粘球菌发育过程中大部分(如果不是全部)蛋白质S的产生。发现含有基因1、基因2或两个基因中插入的黄色粘球菌菌株即使在基因2中含有插入的菌株没有可检测到的蛋白质S时也能正常聚集和形成孢子。我们通过构建大肠杆菌的lacZ基因与黄色粘球菌蛋白质S基因1的N端部分之间的融合体,更详细地研究了基因1的表达。在含有基因融合体的黄色粘球菌菌株中β-半乳糖苷酶活性的表达显示受发育控制。这一结果表明基因1在发育过程中也有表达,尽管显然其水平比基因2低得多。

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