首页> 美国卫生研究院文献>Cell Regulation >IRI-1 a LIN-15B Homologue Interacts with Inositol-145-Triphosphate Receptors and Regulates Gonadogenesis Defecation and Pharyngeal Pumping in Caenorhabditis elegans
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IRI-1 a LIN-15B Homologue Interacts with Inositol-145-Triphosphate Receptors and Regulates Gonadogenesis Defecation and Pharyngeal Pumping in Caenorhabditis elegans

机译:IRI-1一种LIN-15B同源物与肌醇145-三磷酸受体相互作用并调节秀丽隐杆线虫的性腺生成排便和咽部抽水。

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摘要

Inositol-1,4,5-triphosphate receptors (IP3Rs) are ligand-gated Ca2+ channels that control Ca2+ release from intracellular stores. They are central to a wide range of cellular responses. IP3Rs in Caenorhabditis elegans are encoded by a single gene, itr-1, and are widely expressed. Signaling through IP3 and IP3Rs is important in ovulation, control of the defecation cycle, modulation of pharyngeal pumping rate, and embryogenesis. To further elucidate the molecular basis of the diversity of IP3R function, we used a yeast two-hybrid screen to search for proteins that interact with ITR-1. We identified an interaction between ITR-1 and IRI-1, a previously uncharacterized protein with homology to LIN-15B. Iri-1 is widely expressed, and its expression overlaps significantly with that of itr-1. In agreement with this observation, iri-1 functions in known itr-1-mediated processes, namely, upregulation of pharyngeal pumping in response to food and control of the defecation cycle. Knockdown of iri-1 in an itr-1 loss-of-function mutant potentiates some of these effects and sheds light on the signaling pathways that control pharyngeal pumping rate. Knockdown of iri-1 expression also results in a sterile, evl phenotype, as a consequence of failures in early Z1/Z4 lineage divisions, such that gonadogenesis is severely disrupted.
机译:肌醇-1,4,5-三磷酸受体(IP3Rs)是配体门控的Ca 2 + 通道,可控制Ca 2 + 从细胞内存储中释放。它们对于广泛的细胞反应至关重要。秀丽隐杆线虫中的IP3R由单个基因itr-1编码,并被广泛表达。通过IP3和IP3Rs发出信号对于排卵,排便周期控制,咽抽动速率调节和胚胎发生均很重要。为了进一步阐明IP3R功能多样性的分子基础,我们使用了酵母双杂交筛选来寻找与ITR-1相互作用的蛋白质。我们确定了ITR-1和IRI-1之间的相互作用,IRI-1是以前未表征的蛋白,与LIN-15B具有同源性。 Iri-1被广泛表达,其表达与itr-1明显重叠。与该观察结果一致,iri-1在已知的itr-1介导的过程中起作用,即响应食物对咽部抽水的上调和排便周期的控制。降低itr-1功能丧失突变体中的iri-1可以增强其中的某些作用,并阐明控制咽部抽血速率的信号传导途径。由于早期Z1 / Z4谱系分裂失败,导致iri-1表达的抑制还导致无菌的evl表型,从而严重破坏了性腺发育。

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