The Developmental Intestinal Regulator ELT-2 Controls p38-Dependent Immune Responses in Adult C. elegans

被引:40
作者
Block, Dena H. S. [1 ]
Twumasi-Boateng, Kwame [1 ,2 ]
Kang, Hae Sung [1 ]
Carlisle, Jolie A. [1 ]
Hanganu, Alexandru [1 ]
Lai, Ty Yu-Jen [1 ]
Shapira, Michael [1 ,2 ]
机构
[1] Univ Calif Berkeley, Dept Integrat Biol, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Grad Grp Microbiol, Berkeley, CA 94720 USA
来源
PLOS GENETICS | 2015年 / 11卷 / 05期
基金
加拿大自然科学与工程研究理事会;
关键词
GATA TRANSCRIPTION FACTOR; ACTIVATED PROTEIN-KINASES; CAENORHABDITIS-ELEGANS; INNATE IMMUNITY; SIGNALING PATHWAYS; OXIDATIVE STRESS; EXPRESSED GENES; P38; LONGEVITY; EMBRYO;
D O I
10.1371/journal.pgen.1005265
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
GATA transcription factors play critical roles in cellular differentiation and development. However, their roles in mature tissues are less understood. In C. elegans larvae, the transcription factor ELT-2 regulates terminal differentiation of the intestine. It is also expressed in the adult intestine, where it was suggested to maintain intestinal structure and function, and where it was additionally shown to contribute to infection resistance. To study the function of elt-2 in adults we characterized elt-2-dependent gene expression following its knockdown specifically in adults. Microarray analysis identified two ELT-2-regulated gene subsets: one, enriched for hydrolytic enzymes, pointed at regulation of constitutive digestive functions as a dominant role of adult elt-2; the second was enriched for immune genes that are induced in response to Pseudomonas aeruginosa infection. Focusing on the latter, we used genetic analyses coupled to survival assays and quantitative RT-PCR to interrogate the mechanism(s) through which elt-2 contributes to immunity. We show that elt-2 controls p38-dependent gene induction, cooperating with two p38-activated transcription factors, ATF-7 and SKN-1. This demonstrates a mechanism through which the constitutively nuclear elt-2 can impact induced responses, and play a dominant role in C. elegans immunity.
引用
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页数:19
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