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Quantitating transcription factor redundancy: The relative roles of the ELT-2 and ELT-7 GATA factors in the C. elegans endoderm

机译:定量转录因子冗余:线虫内胚层中ELT-2和ELT-7 GATA因子的相对作用

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摘要

The two GATA transcription factors ELT-2 and ELT-7 function in the differentiation of the C. elegans intestine. ELT-2 loss causes lethality. ELT-7 loss causes no obvious phenotype but enhances the elt-2(−) intestinal phenotype. Thus, ELT-2 and ELT-7 appear partially redundant, with ELT-2 being more influential. To investigate the different regulatory roles of ELT-2 and ELT-7, we compared the transcriptional profiles of pure populations of wild-type, elt-2(−), elt-7(−), and elt-7(−); elt-2(−) double mutant L1-stage larvae. Consistent with the mutant phenotypes, loss of ELT-2 had a >25 fold greater influence on the number of significantly altered transcripts compared to the loss of ELT-7; nonetheless, the levels of numerous transcripts changed upon loss of ELT-7 in the elt-2(−) background. The quantitative responses of individual genes revealed a more complicated behaviour than simple redundancy/partial redundancy. In particular, genes expressed only in the intestine showed three distinguishable classes of response in the different mutant backgrounds. One class of genes responded as if ELT-2 is the major transcriptional activator and ELT-7 provides variable compensatory input. For a second class, transcript levels increased upon loss of ELT-2 but decreased upon further loss of ELT-7, suggesting that ELT-7 actually overcompensates for the loss of ELT-2. For a third class, transcript levels also increased upon loss of ELT-2 but remained elevated upon further loss of ELT-7, suggesting overcompensation by some other intestinal transcription factor(s). In spite of its minor loss-of-function phenotype and its limited sequence similarity to ELT-2, ELT-7 expressed under control of the elt-2 promoter is able to rescue elt-2(−) lethality. Indeed, appropriately expressed ELT-7, like appropriately expressed ELT-2, is able to replace all other core GATA factors in the C. elegans endodermal pathway. Overall, this study focuses attention on the quantitative intricacies behind apparent redundancy or partial redundancy of two related transcription factors.
机译:两个GATA转录因子ELT-2和ELT-7在秀丽隐杆线虫肠的分化中起作用。 ELT-2丢失会导致致命性。 ELT-7丢失不会引起明显的表型,但会增强elt-2(-)肠道表型。因此,ELT-2和ELT-7显得部分多余,而ELT-2更具影响力。为了研究ELT-2和ELT-7的不同调节作用,我们比较了野生型,elt-2(-),elt-7(-)和elt-7(-)纯种群的转录谱。 elt-2(-)双突变L1期幼虫。与突变表型一致,ELT-2的丢失对显着改变的转录本数量的影响比ELT-7的丢失大25倍以上。但是,许多转录本的水平在elt-2(-)背景下丢失ELT-7后发生了变化。单个基因的定量反应显示出比简单冗余/部分冗余更复杂的行为。特别地,仅在肠中表达的基因在不同的突变体背景中显示出三种可区分的响应类别。一类基因的反应似乎是ELT-2是主要的转录激活因子,而ELT-7提供了可变的补偿输入。对于第二类,转录水平在ELT-2丢失时增加,但在ELT-7进一步丢失时降低,这表明ELT-7实际上过度补偿了ELT-2的丢失。对于第三类,转录水平在ELT-2缺失时也增加,但在ELT-7进一步缺失时仍保持升高,表明被某些其他肠道转录因子过度补偿。尽管ELT-2具有轻微的功能丧失表型和有限的序列相似性,但在elt-2启动子的控制下表达的ELT-7能够挽救elt-2(-)的致死性。实际上,适当表达的ELT-7和适当表达的ELT-2一样,能够替代秀丽隐杆线虫内胚层途径中的所有其他核心GATA因子。总的来说,这项研究集中在两个相关转录因子的表观冗余或部分冗余背后的定量复杂性上。

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