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可变剪接与起始位点:来自类颗粒头蛋白家族的启示

Alternative splicing and start sites: Lessons from the Grainyhead-like family.

作者信息

Miles Lee B, Dworkin Sebastian, Darido Charbel

机构信息

Department of Physiology, Anatomy and Microbiology, La Trobe University, Bundoora, VIC 3086, Australia.

Division of Cancer Research, Peter MacCallum Cancer Centre, Grattan Street, Parkville, VIC 3052, Australia; Sir Peter MacCallum Department of Oncology, The University of Melbourne, VIC 3052, Australia.

出版信息

Dev Biol. 2017 Sep 1;429(1):12-19. doi: 10.1016/j.ydbio.2017.06.018. Epub 2017 Jun 17.

Abstract

The two main mechanisms that expand the proteomic output of eukaryotic genes are alternative splicing and alternative translation initiation signals. Despite being essential to generate isoforms of gene products that create functional diversity during development, the impact of these mechanisms on fine-tuning regulatory gene networks is still underappreciated. In this review, we use the Grainyhead-like (Grhl) family as a case study to illustrate the importance of isoforms when investigating transcription factor family function during development and disease, and highlight the potential for differential modulation of downstream target genes. We provide insights into the importance of considering alternative gene products when designing, undertaking, and analysing primary research, and the effect that isoforms may have on development. This review also covers known mutations in Grhl family members, and postulates how genetic changes may dictate transcriptional specificity between the Grhl family members. It also contrasts and compares the available literature on the function and importance of the Grhl isoforms, and highlights current gaps in our understanding of their regulatory gene networks in development and disease.

摘要

扩展真核基因蛋白质组输出的两个主要机制是可变剪接和可变翻译起始信号。尽管这些机制对于产生在发育过程中创造功能多样性的基因产物异构体至关重要,但它们对微调调控基因网络的影响仍未得到充分认识。在本综述中,我们以类颗粒头(Grhl)家族为例,说明异构体在研究发育和疾病过程中转录因子家族功能时的重要性,并强调下游靶基因差异调节的潜力。我们深入探讨了在设计、开展和分析基础研究时考虑可变基因产物的重要性,以及异构体可能对发育产生的影响。本综述还涵盖了Grhl家族成员中的已知突变,并推测基因变化如何决定Grhl家族成员之间的转录特异性。它还对比和比较了关于Grhl异构体功能和重要性的现有文献,并突出了我们目前在理解其在发育和疾病中的调控基因网络方面的差距。

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