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来自东亚钳蝎(Buthus martensi Karsch)的三种对钾通道有活性的新型毒素的基因组结构。

Genomic organization of three novel toxins from the scorpion Buthus martensi Karsch that are active on potassium channels.

作者信息

Dai L, Wu J J, Gu Y H, Lan Z D, Ling M H, Chi C W

机构信息

State Key Laboratory of Molecular Biology, Shanghai Institute of Biochemistry, Academia Sinica, Shanghai 200031, People's Republic of China.

出版信息

Biochem J. 2000 Mar 15;346 Pt 3(Pt 3):805-9.

Abstract

The cDNA and genomic DNA of three novel toxins from the scorpion Buthus martensi Karsch that are active on K(+) channels, designated BmKTX (where KTX is kaliotoxin), BmTX1 and BmTX2, were cloned and sequenced. On the basis of their known amino acid sequences, gene-specific primers for 3' and 5' rapid amplification of cDNA ends (RACE) were designed and synthesized. By overlapping the two partial cDNA sequences obtained by 3' and 5' RACE, their full-length cDNA sequences were completed. BmKTX encodes a signal peptide of 22 amino acid residues and a mature toxin of 38 residues, whereas BmTX1 and BmTX2 encode signal peptides of 20 and 21 residues respectively and a mature toxin of 38 residues for each. Their cDNA-deduced amino acid sequences were totally consistent with those determined except that the C-terminus of BmKTX had an additional Gly residue, which was removed during post-translational processing and was indispensable for the amidation of its C-terminal Lys residue. In addition, the first deduced amino acid for both BmTX1 and BmTX2 is Gln instead of pyro-Glu in the reported toxins, which obviously also undergoes post-translational processing. The genomic DNA species of these three toxins were also amplified by PCR, then cloned and sequenced. They all consisted of two exons disrupted by a small single intron. All of these introns were inserted within the signal peptides at position -6 for BmKTX and at position -5 for both BmTX1 and BmTX2 upstream of the mature toxins, and consisted of 87, 87 and 80 bp respectively.

摘要

对来自东亚钳蝎(Buthus martensi Karsch)的三种对钾离子通道有活性的新型毒素的互补DNA(cDNA)和基因组DNA进行了克隆和测序,这三种毒素分别命名为BmKTX(其中KTX是钾离子通道毒素)、BmTX1和BmTX2。根据它们已知的氨基酸序列,设计并合成了用于3'和5' cDNA末端快速扩增(RACE)的基因特异性引物。通过重叠3'和5' RACE获得的两个部分cDNA序列,完成了它们的全长cDNA序列。BmKTX编码一个22个氨基酸残基的信号肽和一个38个残基的成熟毒素,而BmTX1和BmTX2分别编码20个和21个残基的信号肽以及各自一个38个残基的成熟毒素。它们的cDNA推导的氨基酸序列与所测定的序列完全一致,只是BmKTX的C末端有一个额外的甘氨酸残基,该残基在翻译后加工过程中被去除,并且对于其C末端赖氨酸残基酰胺化是必不可少的。此外,BmTX1和BmTX2推导的第一个氨基酸是谷氨酰胺,而不是所报道毒素中的焦谷氨酸,这显然也经历了翻译后加工。这三种毒素的基因组DNA片段也通过聚合酶链反应(PCR)进行了扩增,然后进行克隆和测序。它们均由两个外显子组成,中间被一个小的单内含子隔开。所有这些内含子均插入到成熟毒素上游信号肽内,BmKTX位于 -6位,BmTX1和BmTX2均位于 -5位,长度分别为87、87和80碱基对。

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