Tissue-specific RNA-seq defines genes governing male tail tip morphogenesis in C. elegans.

IF 3.7 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY Development Pub Date : 2024-09-15 Epub Date: 2024-09-24 DOI:10.1242/dev.202787
Karin C Kiontke, R Antonio Herrera, D Adam Mason, Alyssa Woronik, Stephanie Vernooy, Yash Patel, David H A Fitch
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Abstract

Caenorhabditis elegans males undergo sex-specific tail tip morphogenesis (TTM) under the control of the DM-domain 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 versus dmd-3(-) males and hermaphrodites. The transcription profile of dmd-3(-) 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 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 co-regulated by DMD-3, among them the chondroitin synthesis pathway and the hypertonic stress response.

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组织特异性RNA-seq确定了管理秀丽隐杆线虫雄性尾尖形态发生的基因。
雄性秀丽隐杆线虫(Caenorhabditis elegans)在DM-domain转录因子DMD-3的控制下进行性别特异性尾尖形态发生(TTM)。为了找到受DMD-3调控的基因,我们对激光解剖的尾尖进行了RNA-seq分析。我们在野生型雄性与 dmd-3(-)雄性和雌雄同体中发现了 564 个差异表达基因(DE)。dmd-3(-)尾尖的转录谱与雌雄同体相似。为了进行验证,我们分析了 49 个基因的转录报告,发现 26 个基因的表达具有雄性特异性或雄性偏向性。只有 11 个 DE 基因与之前针对 TTM 缺陷的 RNAi 筛选中发现的基因重叠。对 DE 基因的 GO 富集分析发现,未折叠蛋白反应途径中的基因上调,而参与角质层维护的基因下调。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,而且可能是模块化的。我们提出了在 TTM 中共同作用并受 DMD-3 核心调节的基因模块,其中包括软骨素合成途径和高渗应激反应。
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来源期刊
Development
Development 生物-发育生物学
CiteScore
6.70
自引率
4.30%
发文量
433
审稿时长
3 months
期刊介绍: Development’s scope covers all aspects of plant and animal development, including stem cell biology and regeneration. The single most important criterion for acceptance in Development is scientific excellence. Research papers (articles and reports) should therefore pose and test a significant hypothesis or address a significant question, and should provide novel perspectives that advance our understanding of development. We also encourage submission of papers that use computational methods or mathematical models to obtain significant new insights into developmental biology topics. Manuscripts that are descriptive in nature will be considered only when they lay important groundwork for a field and/or provide novel resources for understanding developmental processes of broad interest to the community. Development includes a Techniques and Resources section for the publication of new methods, datasets, and other types of resources. Papers describing new techniques should include a proof-of-principle demonstration that the technique is valuable to the developmental biology community; they need not include in-depth follow-up analysis. The technique must be described in sufficient detail to be easily replicated by other investigators. Development will also consider protocol-type papers of exceptional interest to the community. We welcome submission of Resource papers, for example those reporting new databases, systems-level datasets, or genetic resources of major value to the developmental biology community. For all papers, the data or resource described must be made available to the community with minimal restrictions upon publication. To aid navigability, Development has dedicated sections of the journal to stem cells & regeneration and to human development. The criteria for acceptance into these sections is identical to those outlined above. Authors and editors are encouraged to nominate appropriate manuscripts for inclusion in one of these sections.
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