Elvin C M, Vuocolo T, Smith W J, Eisemann C H, Riddles P W
CSIRO Division of Tropical Animal Production, Indooroopilly, Queensland, Australia.
Insect Mol Biol. 1994 May;3(2):105-15. doi: 10.1111/j.1365-2583.1994.tb00157.x.
A large and diverse family of serine protease genes was identified in first-instar larval cDNA of the sheep blowfly (Lucilia cuprina). This complex repertoire of genes was identified via a PCR approach using highly degenerate primers based on structurally conserved regions which surround the active site His and Ser residues found in all serine proteases. PCR products from entire first-instar larval cDNA, or from third-instar larval salivary glands or cardia, generated using a microscale RT-PCR method, were cloned into a plasmid vector. Comparison of the restriction fragment patterns of PCR products generated from the three different sources suggests a highly diverse tissue-specific pattern of serine protease expression in this organism. Detailed analysis of the restriction fragment patterns of sixty-nine randomly selected clones from entire first-instar larvae revealed forty-nine different classes of PCR product. Maximum likelihood analysis of these data indicate that between 125 and 220 different serine protease genes are expressed in first-instar larvae of L. cuprina. DNA sequence analysis of ten randomly-selected clones, derived from the three tissue sources, indicated that all ten encoded serine protease gene fragments. A frequently occurring PCR product, generated from both first-instar total cDNA and third-instar cardia cDNA, showed 73% amino acid identity to a digestive protease expressed in Drosophila melanogaster larval gut cells.
在羊绿蝇(Lucilia cuprina)一龄幼虫的cDNA中鉴定出了一个庞大且多样的丝氨酸蛋白酶基因家族。这个复杂的基因库是通过PCR方法鉴定出来的,该方法使用了基于所有丝氨酸蛋白酶活性位点组氨酸和丝氨酸残基周围结构保守区域的高度简并引物。使用微量RT-PCR方法从整个一龄幼虫cDNA或三龄幼虫唾液腺或贲门产生的PCR产物被克隆到质粒载体中。对来自三种不同来源的PCR产物的限制性片段模式进行比较,表明该生物体中丝氨酸蛋白酶表达具有高度多样的组织特异性模式。对从整个一龄幼虫中随机选择的69个克隆的限制性片段模式进行详细分析,揭示了49种不同类别的PCR产物。对这些数据的最大似然分析表明,在羊绿蝇一龄幼虫中表达了125至220个不同的丝氨酸蛋白酶基因。对来自三种组织来源的10个随机选择的克隆进行DNA序列分析,表明所有10个克隆都编码丝氨酸蛋白酶基因片段。一种常见的PCR产物,由一龄幼虫总cDNA和三龄幼虫贲门cDNA产生,与在黑腹果蝇幼虫肠道细胞中表达的一种消化蛋白酶具有73%的氨基酸同一性。