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全基因组范围内启动子附近甲基化障碍的筛选和功能验证。

Genome-wide screening and functional validation of methylation barriers near promoters.

机构信息

College of Health Solutions, Arizona State University, Phoenix, AZ, USA.

Center for Personalized Diagnostics, Biodesign Institute, Arizona State University, Tempe, AZ, USA.

出版信息

Nucleic Acids Res. 2024 May 22;52(9):4857-4871. doi: 10.1093/nar/gkae302.

Abstract

CpG islands near promoters are normally unmethylated despite being surrounded by densely methylated regions. Aberrant hypermethylation of these CpG islands has been associated with the development of various human diseases. Although local genetic elements have been speculated to play a role in protecting promoters from methylation, only a limited number of methylation barriers have been identified. In this study, we conducted an integrated computational and experimental investigation of colorectal cancer methylomes. Our study revealed 610 genes with disrupted methylation barriers. Genomic sequences of these barriers shared a common 41-bp sequence motif (MB-41) that displayed homology to the chicken HS4 methylation barrier. Using the CDKN2A (P16) tumor suppressor gene promoter, we validated the protective function of MB-41 and showed that loss of such protection led to aberrant hypermethylation. Our findings highlight a novel sequence signature of cis-acting methylation barriers in the human genome that safeguard promoters from silencing.

摘要

CpG 岛位于启动子附近,尽管周围被高度甲基化区域环绕,但通常是非甲基化的。这些 CpG 岛的异常高甲基化与多种人类疾病的发展有关。虽然局部遗传元件被推测在保护启动子免受甲基化方面发挥作用,但只有有限数量的甲基化障碍被鉴定出来。在这项研究中,我们对结直肠癌甲基组进行了综合计算和实验研究。我们的研究揭示了 610 个具有破坏的甲基化障碍的基因。这些障碍的基因组序列共享一个常见的 41 个碱基对序列基序(MB-41),与鸡 HS4 甲基化障碍具有同源性。使用 CDKN2A(P16)肿瘤抑制基因启动子,我们验证了 MB-41 的保护功能,并表明这种保护的丧失导致异常的高甲基化。我们的发现强调了人类基因组中顺式作用甲基化障碍的新型序列特征,这些特征可以保护启动子免受沉默。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0ca/11109949/09b8532c97ba/gkae302figgra1.jpg

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