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遗传密码1990。展望。

Genetic code 1990. Outlook.

作者信息

Jukes T H

机构信息

Space Sciences Laboratory, University of California/Berkeley, Oakland 94608.

出版信息

Experientia. 1990 Dec 1;46(11-12):1149-57. doi: 10.1007/BF01936925.

Abstract

The genetic code is evolving as shown by 9 departures from the universal code: 6 of them are in mitochondria and 3 are in nuclear codes. We propose that these changes are preceded by disappearance of a codon from coding sequences in mRNA of an organism or organelle. The function of the codon that disappears is taken by other, synonymous codons, so that there is no change in amino acid sequences of proteins. The deleted codon then reappears with a new function. Wobble pairing between anticodons and codons has evolved, starting with a single UNN anticodon pairing with 4 codons. Directional mutation pressure affects codon usage and may produce codon reassignments, especially of stop codons. Selenocysteine is coded by UGA, which is also a stop codon, and this anomaly is discussed. The outlook for discovery of more changes in the code is favorable, and open reading frames should be compared with actual sequential analyses of protein molecules in this search.

摘要

遗传密码正在演变,这体现在与通用密码存在9处差异:其中6处存在于线粒体中,3处存在于核密码中。我们提出,这些变化之前,生物体或细胞器的mRNA编码序列中的一个密码子会消失。消失的密码子的功能由其他同义密码子承担,因此蛋白质的氨基酸序列不会发生变化。随后,缺失的密码子会以新的功能重新出现。反密码子与密码子之间的摆动配对已经进化,最初是单个UNN反密码子与4个密码子配对。定向突变压力影响密码子使用,可能导致密码子重新分配,尤其是终止密码子。硒代半胱氨酸由UGA编码,而UGA也是一个终止密码子,本文对此异常情况进行了讨论。发现密码中更多变化的前景是乐观的,在这一探索过程中,应将开放阅读框与蛋白质分子的实际序列分析进行比较。

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