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保守的Myc框2和Myc框3区域对于Myc在体内的功能很重要,但并非必不可少。

The conserved Myc box 2 and Myc box 3 regions are important, but not essential, for Myc function in vivo.

作者信息

Schwinkendorf D, Gallant P

机构信息

Zoologisches Institut, Universität Zürich, Zürich, Switzerland.

出版信息

Gene. 2009 May 1;436(1-2):90-100. doi: 10.1016/j.gene.2009.02.009. Epub 2009 Feb 24.

Abstract

Myc proto-oncoproteins are important regulators of growth and proliferation in development. Their functions have been evolutionarily conserved from insects to vertebrates, although the sequence conservation is limited to a few short domains. Here, we analyze the requirement for the most highly conserved domains, called Myc boxes 2 and 3 (MB2 and MB3), and for the weakly conserved N-terminus for the biological activity of the single Drosophila Myc protein in the animal in vivo. We find that a Myc mutant lacking the N-terminus retains very little activity, whereas Myc transgenes carrying a deletion of MB3 have a moderately increased ability to promote growth and apoptosis; mutation of MB2 reduces transcriptional output and the biological activities of Myc. Surprisingly though, Myc without MB2 retains enough activity to partially rescue the lethality of a Myc null mutation. Thus, although MB2 and MB3 are highly conserved in evolution, loss of either domain has comparatively mild consequences on Myc activity in vivo.

摘要

Myc原癌蛋白是发育过程中生长和增殖的重要调节因子。尽管序列保守性仅限于少数短结构域,但它们的功能从昆虫到脊椎动物在进化上是保守的。在这里,我们分析了果蝇体内单个Myc蛋白的生物活性对最保守的结构域(称为Myc框2和3,即MB2和MB3)以及弱保守的N端的需求。我们发现,缺失N端的Myc突变体活性极低,而携带MB3缺失的Myc转基因促进生长和凋亡的能力适度增加;MB2的突变会降低转录输出和Myc的生物活性。然而,令人惊讶的是,没有MB2的Myc仍保留足够的活性来部分挽救Myc基因敲除突变的致死性。因此,尽管MB2和MB3在进化中高度保守,但任一结构域的缺失对Myc在体内的活性影响相对较小。

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