ELL2 影响转录延伸、剪接、Ig 分泌和生长。

Journal of mucosal immunology research Pub Date : 2019-01-01 Epub Date: 2019-07-12
Anthony Ghobrial, Nathaniel Flick, Ryan Daly, Malcolm Hoffman, Christine Milcarek
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摘要

ELL2 以前是作为超级延伸复合体的一个成员被发现的。它通过改变 RNA 处理模式,促进与浆细胞相关的重链免疫球蛋白(IgH)分泌形式的生成,从而参与推动 B 细胞向浆细胞的成熟。ELL2 影响抗体分泌细胞中 4,000 多个基因的表达和剪接模式。ELL2 基因与多发性骨髓瘤和唾液腺癌等癌症有关。最近证明,ELL 家族的一个成员(ELL1)通过 C 端 CEYLH 区域的一个高度保守的半胱氨酸残基,作为 E3 泛素连接酶作用于已知的原癌基因 c-Myc。序列同源性比较显示,该区域在 ELL 家族的三个成员之间是保守的,因此我们推测另外两个 ELL(2 号和 3 号)也能发挥同样的作用。在这篇综述中,我们总结了有关 ELL2 的已知信息,包括它在推动 B 细胞向浆细胞分化方面的作用,以及它在抑制肿瘤方面的潜在作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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ELL2 Influences Transcription Elongation, Splicing, Ig Secretion and Growth.

ELL2 was previously discovered as a member of the Super Elongation Complex. It is involved in driving the maturation of B cells to plasma cells through shifting patterns of RNA processing, favoring generation of the secretory form of heavy chain immunoglobulin (IgH) associated with plasma cells. ELL2 influences the expression and splicing patterns of more than 4,000 genes in antibody secreting cells. The ELL2 gene has been implicated in cancers such as multiple myeloma and salivary gland carcinoma. A member of the ELL family (ELL1) was recently proven to act as an E3 ubiquitin ligase to known proto-oncogene, c-Myc, through a highly conserved cysteine residue in the C-terminal CEYLH region. Comparison of sequence homology shows this region is conserved between the three members of the ELL family, leading us to hypothesize that the other two ELLs (2 and 3) could serve the same role. In this review, we summarize what is known about ELL2 with respect to its role in driving B cell to plasma cell differentiation as well as its potential role in tumor suppression.

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