Douglas Susan E, Patrzykat Aleksander, Pytyck Jennifer, Gallant Jeffrey W
Institute for Marine Biosciences, Halifax, Nova Scotia, Canada.
Eur J Biochem. 2003 Sep;270(18):3720-30. doi: 10.1046/j.1432-1033.2003.03758.x.
Antimicrobial peptides form one of the first lines of defense against invading pathogens by killing the microorganisms and/or mobilizing the host innate immune system. Although over 800 antimicrobial peptides have been isolated from many different species, especially insects, few have been reported from marine fish. Sequence analysis of two genomic clones (15.6 and 12.5 kb) from the winter flounder, Pseudopleuronectes americanus (Walbaum) resulted in the identification of multiple clustered genes for novel pleurocidin-like antimicrobial peptides. Four genes and three pseudogenes (Psi) are encoded in these clusters, all of which have similar intron/exon boundaries but specify putative antimicrobial peptides differing in sequence. Pseudogenes are easily detectable but have incorrect initiator codons (ACG) and often contain a frameshift(s). Potential promoters and binding sites for transcription factors implicated in regulation of expression of immune-related genes have been identified in upstream regions by comparative genomics. Using reverse transcription-PCR assays, we have shown for the first time that each gene is expressed in a tissue-specific and developmental stage-specific manner. In addition, synthetic peptides based on the sequences of both genes and pseudogenes have been produced and tested for antimicrobial activity. These data can be used as a basis for prediction of antimicrobial peptide candidates for both human and nonhuman therapeutants from genomic sequences and will aid in understanding the evolution and transcriptional regulation of expression of these peptides.
抗菌肽通过杀死微生物和/或调动宿主先天免疫系统,构成抵御入侵病原体的第一道防线之一。尽管已从许多不同物种,尤其是昆虫中分离出800多种抗菌肽,但从海洋鱼类中报道的却很少。对美洲拟庸鲽(Pseudopleuronectes americanus,Walbaum)的两个基因组克隆(15.6和12.5 kb)进行序列分析,鉴定出了多个新的类pleurocidin抗菌肽的成簇基因。这些簇中编码了四个基因和三个假基因(Psi),它们都具有相似的内含子/外显子边界,但所推测的抗菌肽序列不同。假基因很容易检测到,但起始密码子不正确(ACG),并且通常包含移码。通过比较基因组学,在上游区域已鉴定出与免疫相关基因表达调控有关的潜在启动子和转录因子结合位点。使用逆转录-聚合酶链反应分析,我们首次表明每个基因都以组织特异性和发育阶段特异性的方式表达。此外,已根据基因和假基因的序列合成了肽,并测试了其抗菌活性。这些数据可作为从基因组序列预测人类和非人类治疗用抗菌肽候选物的基础,并将有助于理解这些肽的进化和转录调控表达。