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细柱晶囊轮虫中两个β-微管蛋白基因的核苷酸序列与表达

Nucleotide sequence and expression of two beta-tubulin genes in Stylonychia lemnae.

作者信息

Conzelmann K K, Helftenbein E

机构信息

Universität Tübingen, Abt. Zellbiologie, F.R.G.

出版信息

J Mol Biol. 1987 Dec 20;198(4):643-53. doi: 10.1016/0022-2836(87)90207-5.

Abstract

The gene-sized macronuclear DNA of the hypotrichous ciliate Stylonychia lemnae contains one size class of DNA molecules of 1.85 kb (1 kb = 10(3) base-pairs) coding for beta-tubulin. These DNA molecules consist of two different beta-tubulin genes, beta 1 and beta 2, which are amplified to about 150,000 (beta 1) and 30,000 (beta 2) copies per macronucleus. Both genes were cloned and sequenced entirely. The coding sequences of the two molecules (1329 base-pairs including TGA) predict identical amino acid sequences for the proteins and show a nucleotide homology of 97.2%. The nucleotide as well as the encoded amino acid sequences are highly conserved, when compared to beta-tubulin genes from vertebrates. The ciliate-specific codon TAA specifying glutamine is present only in the beta 2-tubulin gene, whereas glutamine is encoded soley by CAA in the beta 1-tubulin gene. The 5' and 3'-non-coding regions of both beta-tubulin genes are similar in length, but differ extremely in nucleotide sequence. Both beta-tubulin genes are transcriptionally active in S. lemnae, although not all putative transcription-regulatory sequences known from higher eukaryotes can be detected within the non-coding regions. The two transcription products localized by S1-mapping experiments show a similar length of about 1.40 kb and transcription seems to be regulated differently for beta 1 and beta 2.

摘要

纤毛亚纲的纤细裸藻的基因大小的大核DNA含有一类大小为1.85 kb(1 kb = 10³个碱基对)的DNA分子,编码β-微管蛋白。这些DNA分子由两个不同的β-微管蛋白基因β1和β2组成,每个大核中β1基因扩增到约150,000个拷贝,β2基因扩增到约30,000个拷贝。两个基因都被完全克隆并测序。两个分子的编码序列(包括TGA共1329个碱基对)预测的蛋白质氨基酸序列相同,核苷酸同源性为97.2%。与脊椎动物的β-微管蛋白基因相比,核苷酸以及编码的氨基酸序列高度保守。特定于纤毛虫的编码谷氨酰胺的密码子TAA仅存在于β2-微管蛋白基因中,而在β1-微管蛋白基因中谷氨酰胺仅由CAA编码。两个β-微管蛋白基因的5'和3'-非编码区长度相似,但核苷酸序列差异极大。两个β-微管蛋白基因在纤细裸藻中都具有转录活性,尽管在非编码区中未检测到所有从高等真核生物中已知的推定转录调控序列。通过S1映射实验定位的两种转录产物长度相似,约为1.40 kb,并且β1和β2的转录调控似乎有所不同。

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