Identification and evolution of two insulin receptor genes involved in Tribolium castaneum development and reproduction

被引:52
作者
Sang, Ming [1 ]
Li, Chengjun [1 ]
Wu, Wei [1 ]
Li, Bin [1 ]
机构
[1] Nanjing Normal Univ, Coll Life Sci, Jiangsu Key Lab Biodivers & Biotechnol, Nanjing 210023, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Insulin receptor; Evolution; RNA interference; Development; Reproduction; Tribolium castaneum; RED FLOUR BEETLE; EXTENDS LIFE-SPAN; SIGNALING PATHWAY; TYROSINE KINASE; HONEY-BEE; EXPRESSION; GROWTH; PEPTIDES; HOMOLOG; TRANSDUCTION;
D O I
10.1016/j.gene.2016.02.034
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The insulin and insulin-like signaling (IIS) pathway exists in a wide range of organisms from mammals to invertebrates and regulates several vital physiological functions. A phylogenetic analysis have indicated that insulin receptors have been duplicated at least twice among vertebrates, whereas only one duplication occurred in insects before the differentiation of Coleoptera, Hymenoptera, and Hemiptera. Thus, we cloned two putative insulin receptor genes, Tcas-ir1 and T.cas-ir2, from T. castaneum and determined that Tcas-ir1 is most strongly expressed during the late adult and early pupal stages, whereas T.cas-ir2 is most strongly expressed during the late larval stage. We found that larval RNAi against T.cas-ir1 and Tcas-ir2 causes 100% and 42.0% insect death, respectively, and that parental RNAi against T.cas-ir1 and T.cas-ir2 leads to 100% and 33.3% reductions in beetle fecundity, respectively. The hatching rate of ds-ir2 insects was 66.2%. Moreover, ANAL against these two genes increased the expression of the pkc, foxo, jnk, cdc42, ikk, and mekk genes but decreased erk gene expression. Despite these similarities, these two genes act via distinct regulatory pathways. These results indicate that these two receptors have functionally diverged with respect to the development and reproduction of T. castaneum, even though they retain some common regulatory signaling pathways. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:196 / 204
页数:9
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