Kiontke Karin, Herrera R Antonio, Mason D Adam, Woronik Alyssa, Vernooy Stephanie, Patel Yash, Fitch David H A
Department of Biology, New York University, 100 Washington Square E., New York, NY 10003.
Baylor School, 171 Baylor School Road, Chattanooga, TN 37405.
bioRxiv. 2024 Jan 12:2024.01.12.575210. doi: 10.1101/2024.01.12.575210.
males undergo sex-specific tail tip morphogenesis (TTM) under the control of the transcription factor DMD-3. To find genes regulated by DMD-3, We performed RNA-seq of laser-dissected tail tips. We identified 564 genes differentially expressed (DE) in wild-type males vs. - males and hermaphrodites. The transcription profile of - tail tips is similar to that in hermaphrodites. For validation, we analyzed transcriptional reporters for 49 genes and found male-specific or male-biased expression for 26 genes. Only 11 DE genes overlapped with genes found in a previous RNAi screen for defective TTM. GO enrichment analysis of DE genes finds upregulation of genes within the UPR (unfolded protein response) pathway and downregulation of genes involved in cuticle maintenance. Of the DE genes, 40 are transcription factors, indicating that the gene network downstream of DMD-3 is complex and potentially modular. We propose modules of genes that act together in TTM and are coregulated by DMD-3, among them the chondroitin synthesis pathway and the hypertonic stress response.
雄性在转录因子DMD-3的控制下经历性别特异性的尾尖形态发生(TTM)。为了找到受DMD-3调控的基因,我们对激光切割的尾尖进行了RNA测序。我们鉴定出564个在野生型雄性与[缺失信息]雄性和雌雄同体中差异表达(DE)的基因。[缺失信息]尾尖的转录谱与雌雄同体中的相似。为了验证,我们分析了49个基因的转录报告基因,发现26个基因有雄性特异性或雄性偏向性表达。只有11个DE基因与先前针对缺陷TTM的RNAi筛选中发现的基因重叠。对DE基因的GO富集分析发现未折叠蛋白反应(UPR)途径中的基因上调,而参与角质层维持的基因下调。在DE基因中,有40个是转录因子,这表明DMD-3下游的基因网络是复杂的,并且可能是模块化的。我们提出了在TTM中共同起作用并由DMD-3共同调控的基因模块,其中包括硫酸软骨素合成途径和高渗应激反应。