Abete-Luzi Patricia, Eisenmann David M
Department of Biological Sciences, University of Maryland Baltimore County, Baltimore, Maryland, 21250.
Genesis. 2018 May;56(5). doi: 10.1002/dvg.23106. Epub 2018 Apr 23.
The cuticle, the outer covering of the nematode C. elegans, is synthesized five times during the worm's life by the underlying hypodermis. Cuticle collagens, the major cuticle component, are encoded by a large family of col genes and, interestingly, many of these genes express predominantly at a single developmental stage. This temporal preference motivated us to investigate the mechanisms underlying col gene expression and here we focus on a subset of col genes expressed in the L4 stage. We identified minimal promoter regions of <300 bp for col-38, col-49, and col-63. In these regions, we predicted cis-regulatory sequences and evaluated their function in vivo via mutagenesis of a col-38p::yfp reporter. We used RNAi to study the requirement for candidate transcription regulators ELT-1 and ELT-3, LIN-29, and the LIN-29 co-factor MAB-10, and found LIN-29 to be necessary for the expression of four L4-specific genes (col-38, col-49, col-63, and col-138). Temporal misexpression of LIN-29 was also sufficient to activate these genes at a different developmental stage. The LIN-29 DNA-binding domain bound the col-38, col-49, and col-63 minimal promoters in vitro. For col-38 we showed that the LIN-29 sites necessary for reporter expression in vivo are also bound in vitro: this is the first identification of specific binding sites for LIN-29 necessary for in vivo target gene expression.
线虫秀丽隐杆线虫的角质层是其外部覆盖物,在蠕虫的生命周期中由其下方的皮下组织合成五次。角质层胶原蛋白是角质层的主要成分,由一大类col基因编码,有趣的是,这些基因中的许多主要在单个发育阶段表达。这种时间偏好促使我们研究col基因表达的潜在机制,在这里我们专注于在L4阶段表达的col基因的一个子集。我们确定了col-38、col-49和col-63的小于300 bp的最小启动子区域。在这些区域中,我们预测了顺式调控序列,并通过对col-38p::yfp报告基因进行诱变来评估它们在体内的功能。我们使用RNA干扰来研究候选转录调节因子ELT-1和ELT-3、LIN-29以及LIN-29辅助因子MAB-10的需求,发现LIN-29对于四个L4特异性基因(col-38、col-49、col-63和col-138)的表达是必需的。LIN-29的时间错误表达也足以在不同的发育阶段激活这些基因。LIN-29 DNA结合结构域在体外与col-38、col-49和col-63的最小启动子结合。对于col-38,我们表明体内报告基因表达所需的LIN-29位点在体外也能结合:这是首次鉴定出体内靶基因表达所需的LIN-29的特异性结合位点。