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斑点叉尾鮰(Ictalurus punctatus)生长激素基因的结构及其进化意义。

Structure of the channel catfish (Ictalurus punctatus) growth hormone gene and its evolutionary implications.

作者信息

Tang Y, Lin C M, Chen T T, Kawauchi H, Dunham R A, Powers D A

机构信息

Department of Microbiology, University of Maryland, College Park 20742.

出版信息

Mol Mar Biol Biotechnol. 1993 Aug;2(4):198-206.

PMID:8293072
Abstract

A DNA fragment of 1.6 kilo base pairs (kb), encoding part of the channel catfish (Ictalurus punctatus) growth hormone (GH) gene, was generated by the polymerase chain reaction (PCR) using 2 degenerate synthetic oligonucleotides (30 and 33 mer) derived from the N- and C-terminal amino acid sequences of the catfish GH polypeptide as amplification primers and with catfish genomic DNA as a template. This DNA fragment was used as a probe for the isolation of a catfish GH gene from a genomic library constructed in a lambda phage cloning vector, lambda Dash II. Three positive clones were isolated, and their complete nucleotide sequences were determined. Nucleotide sequences from clones 1 and 3 were identical, whereas clone 2 had 2 base substitutions. The gene spans approximately 3 kb and is comprised of 5 exons and 4 introns. The initiation codon, the termination codon, and the canonical polyadenylation sequence were identified. The amino acid sequence deduced from the predicted coding region of the gene is in agreement with that of the native GH polypeptide sequence. A sequence (TATAAAA) matching the TATA box consensus sequence was located at nucleotide positions -30 to -23. Furthermore, 2 sequences corresponding to the mammalian Pit-1/GHF-1 binding sites (consensus sequence TT[AA]TATNCAT) were identified in the 5' flanking region starting at positions -113 and -134. Another sequence (GTACCAGTGA) conserved among the GH genes of the channel catfish and other known animal species was also identified at position -220. The biological functions of this sequence remain to be determined.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

利用聚合酶链反应(PCR),以2条简并合成寡核苷酸(分别为30聚体和33聚体)为扩增引物,这两条引物来源于鲶鱼生长激素(GH)多肽的N端和C端氨基酸序列,同时以鲶鱼基因组DNA为模板,产生了一个1.6千碱基对(kb)的DNA片段,该片段编码斑点叉尾鮰(Ictalurus punctatus)生长激素(GH)基因的一部分。这个DNA片段被用作探针,从构建于λ噬菌体克隆载体λ Dash II中的基因组文库中分离鲶鱼GH基因。分离出3个阳性克隆,并测定了它们的完整核苷酸序列。克隆1和克隆3的核苷酸序列相同,而克隆2有2个碱基替换。该基因跨度约3 kb,由5个外显子和4个内含子组成。确定了起始密码子、终止密码子和典型的聚腺苷酸化序列。从该基因预测编码区推导的氨基酸序列与天然GH多肽序列一致。一个与TATA框共有序列匹配的序列(TATAAAA)位于核苷酸位置-30至-23处。此外,在5'侧翼区域从位置-113和-134开始鉴定出2个与哺乳动物Pit-1/GHF-1结合位点相对应的序列(共有序列TT[AA]TATNCAT)。在-220位置还鉴定出另一个在斑点叉尾鮰和其他已知动物物种的GH基因中保守的序列(GTACCAGTGA)。该序列的生物学功能有待确定。(摘要截短至250字)

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