Iwamuro Shawichi, Kobayashi Tetsuya
Department of Biology, Faculty of Science, Toho University, Funabashi, Chiba, Japan.
Methods Mol Biol. 2010;615:159-76. doi: 10.1007/978-1-60761-535-4_13.
Antimicrobial peptides (AMPs) play an important role in the host's innate defence system in many organisms. Amphibian skin is expected to be a particularly rich source of novel AMPs. In amphibians, AMPs are produced from precursor proteins via specific cleavage by processing enzymes. While the nucleotide sequences of the AMP coding region in precursors are hypervariable, those of other regions, including the 5(')- and 3(')-untranslated regions (UTRs), are highly or relatively conserved in different precursors. Such nucleotide sequence conservation suggests an efficient strategy for molecular cloning of the antimicrobial peptide genes by 3(')-rapid amplification of cDNA ends (3(')-RACE) and reverse transcriptase polymerase chain reaction (RT-PCR) methods using specific primers. With this strategy in mind we have established an efficient protocol suitable for amplification of multiple cDNAs encoding amphibian AMP precursor proteins.
抗菌肽(AMPs)在许多生物体的宿主天然防御系统中发挥着重要作用。两栖动物的皮肤有望成为新型抗菌肽的特别丰富来源。在两栖动物中,抗菌肽由前体蛋白通过加工酶的特异性切割产生。虽然前体中抗菌肽编码区的核苷酸序列高度可变,但其他区域的序列,包括5′和3′非翻译区(UTRs),在不同的前体中高度或相对保守。这种核苷酸序列保守性提示了一种通过使用特异性引物的3′-cDNA末端快速扩增(3′-RACE)和逆转录聚合酶链反应(RT-PCR)方法来分子克隆抗菌肽基因的有效策略。基于这一策略,我们建立了一种适用于扩增多个编码两栖动物抗菌肽前体蛋白的cDNA的有效方案。