Regulation of a serine protease homolog by the JNK pathway during thoracic development of Drosophila melanogaster

被引:9
|
作者
Srivastava, Ajay [1 ,2 ,3 ]
Dong, Qian [2 ,3 ]
机构
[1] Yale Univ, Dept Genet, New Haven, CT USA
[2] Western Kentucky Univ, Dept Biol, Bowling Green, KY 42101 USA
[3] Western Kentucky Univ, Ctr Biotechnol, Bowling Green, KY 42101 USA
来源
FEBS OPEN BIO | 2015年 / 5卷
基金
美国国家卫生研究院;
关键词
Drosophila; JNK pathway; Thorax closure; Serine protease homolog; Imaginal disc; Scarface; BASEMENT-MEMBRANE; GENE-EXPRESSION; DISC EVERSION; MORPHOGENESIS; SCARFACE; CLOSURE; FOS;
D O I
10.1016/j.fob.2015.01.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The importance of the Jun N-terminal Kinase (JNK) pathway during normal development and tumor invasion has been well documented in Drosophila. Here, this pathway plays important roles in epithelial morphogenesis, wound healing, apoptosis, immunity and regulation of lifespan. However, which downstream molecules facilitate these effects is not very well elucidated. In this study, data are presented on a serine protease homolog (SPH), scarface. These data show that scarface is under regulatory control of the JNK pathway and that this pathway is both necessary and sufficient for its expression within the context of thoracic development. Consequently, down-regulation of scarface results in a thoracic-cleft phenotype that phenocopies the JNK pathway defect. A possible role of scarface during thoracic development in Drosophila is discussed. (C) 2015 The Authors. Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies. This is an open access article under the CC BY-NC-ND license
引用
收藏
页码:117 / 123
页数:7
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