SOX2OT, a long non-coding RNA involved in autophagy regulation

M. S. Jazi
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Abstract

Human SOX2OT, located in chromosome 3q26.3 encodes for a nonprotein coding long RNA with different alternative splice variants (1). It was discovered as a gene associated with eye developmental disorders including microphthalmia and anophthalmia (2). The function of SOX2OT has been under investigation since its discovery. It has been shown that SOX2OT can regulate the embryonic stem cell in vertebrate (3) and also it has higher expression level in different tumor types taking role in pathogenesis of cancers(4). Article Type: Letter to Editor
人类SOX2OT位于染色体3q26.3,编码具有不同剪接变体的非蛋白编码长RNA(1)。该基因被发现与眼发育障碍(包括小眼症和眼失症)相关(2)。自发现以来,人们一直在研究SOX2OT的功能。研究表明SOX2OT可以调控脊椎动物的胚胎干细胞(3),并且在不同的肿瘤类型中具有较高的表达水平,在癌症的发病机制中发挥作用(4)。文章类型:致编辑信
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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