Oustitch T L, Peters L E, Utkin Yu N, Tsetlin V I
Eppendorf 5 Prime, Inc., 6531 Gunbarrel Av., Boulder, CO 80301, USA.
IUBMB Life. 2003 Jan;55(1):43-7. doi: 10.1080/1521654021000061664.
Selective cloning of the cDNA coding for a weak neurotoxin (WTX) from cobra N. kaouthia including the 5'- and 3'-non-translated regions (NTR) is described. The known amino acid sequence of WTX was used together with the nucleotide sequence of a weak neurotoxin NNAM2 from cobra Naja atra, to design WTX-specific primers for direct amplification of an internal WTX cDNA fragment by RT- PCR. The sequence of the complete WTX cDNA was determined in sequencing runs on internal PCR products, cloned 3'- and 5'-RACE-fragments and several full-length cDNA clones. The cDNA coding sequence is in excellent agreement with the previously determined WTX amino acid sequence, has a high homology with other known weak toxin cDNAs, whereas even higher homology (up to 96%) with several classes of 3-finger toxins was detected in the 59 bp 3'-NTR consensus sequence. A possible function of the highly conserved nucleotide sequence elements is discussed.
描述了从眼镜蛇舟山眼镜蛇中选择性克隆编码弱神经毒素(WTX)的cDNA,包括5'-和3'-非翻译区(NTR)。使用WTX已知的氨基酸序列以及眼镜蛇中华眼镜蛇弱神经毒素NNAM2的核苷酸序列,设计WTX特异性引物,通过RT-PCR直接扩增WTX内部cDNA片段。完整WTX cDNA的序列通过对内部PCR产物、克隆的3'-和5'-RACE片段以及几个全长cDNA克隆进行测序来确定。cDNA编码序列与先前确定的WTX氨基酸序列高度一致,与其他已知弱毒素cDNA具有高度同源性,而在59 bp 3'-NTR共有序列中检测到与几类三指毒素的同源性更高(高达96%)。讨论了高度保守的核苷酸序列元件的可能功能。