在daf-16突变体daer幼虫中,Hbl-1不会导致成体细胞命运标记的错误表达。

microPublication biology Pub Date : 2025-06-24 eCollection Date: 2025-01-01 DOI:10.17912/micropub.biology.001662
Matthew J Wirick, Xantha Karp
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引用次数: 0

摘要

在隐杆线虫幼虫中,FOXO同源物daf-16在外侧皮下反对col-19p::gfp成体细胞命运标记的表达。Daf-16部分通过lin-41起作用,lin-41是一种在非发育过程中促进幼虫缝细胞命运的异慢性基因。在这里,我们发现一个不同的异慢性基因,hbl-1,在daf-16的下游不发挥作用来调节冷-19p::gfp的表达。功能获得型hbl-1等位基因在daf-16 (0) daer幼虫中没有抑制异位col19p::gfp的表达,并且在对照组和daf-16 (0) daer幼虫中未检测到hbl-1蛋白。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
hbl-1 does not contribute to the misexpression of an adult cell fate marker in daf-16 mutant dauer larvae.

In Caenorhabditis elegans dauer larvae, the FOXO ortholog, daf-16 , opposes the expression of the col-19p::gfp adult cell fate marker in the lateral hypodermis. daf-16 acts in part via lin-41 , a heterochronic gene that promotes larval seam cell fate during non-dauer development. Here, we show that a different heterochronic gene, hbl-1 , does not function downstream of daf-16 to regulate col-19p::gfp expression during dauer. A gain-of-function hbl-1 allele did not suppress ectopic col-19p::gfp expression in daf-16 (0) dauer larvae, and HBL-1 protein was not detectable in control or daf-16 (0) dauer larvae.

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