Characterization of a novel cDNA encoding a short venom peptide derived from venom gland of scorpion Buthus martensii Karsch:: Trans-splicing may play an important role in the diversification of scorpion venom peptides

被引:14
作者
Zeng, XC [1 ]
Luo, F [1 ]
Li, WX [1 ]
机构
[1] Wuhan Univ, Coll Life Sci, Dept Biotechnol, Inst Virol,State Key Lab Virol, Wuhan 430072, Peoples R China
关键词
trans-splicing; venom peptide; evolution; peptide diversity; scorpion; Buthus martensii Karsch; intron; Na+-channel specific toxin;
D O I
10.1016/j.peptides.2005.07.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A novel cDNA clone (named BmKT-u) which is a hybrid molecule of the 5'-terminal region of BmKT' cDNA and the 3'-terminal region of an undocumented cDNA (named BmKu), was isolated from a cDNA library made from the venom gland of scorpion Buthus martensii Karsch. BmKT-u codes for a 30 amino acid residue precursor peptide composed of a 20-residue signal sequence, and a putative 10-residue novel mature peptide. Northern blot hybridization showed BmKT-u cDNA is generated from a transcript. RT-PCR experiments excluded the possibility that BmKT-u cDNA is an artifact generated during reverse transcription. Genomic amplifications performed with three pairs of BmKT-u gene-specific primers showed the BmKT-u gene does not exist in the genome of the scorpion as a single transcriptional unit. Genomic cloning for BmKT' showed that the BmKT' gene contains an intron of 509bp inserted into the region encoding the C-terminal region of the signal peptide. A sequence alignment comparison of the cDNA of BmKT-u with genomic BmKT' revealed that the junction site of the hybrid molecule is located at the 5'-splicing site of the intron. The data suggest that the BmKT-u transcript is a naturally occurring mature mRNA that is generated by trans-splicing. Trans-splicing may contribute to the diversity of venom peptides from venomous animals. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:675 / 681
页数:7
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