4.7 Article

A Global Vista of the Epigenomic State of the Mouse Submandibular Gland

期刊

JOURNAL OF DENTAL RESEARCH
卷 100, 期 13, 页码 1492-1500

出版社

SAGE PUBLICATIONS INC
DOI: 10.1177/00220345211012000

关键词

salivary glands; ChIP-sequencing; histone modification; gene expression; epigenomics; regulatory regions

资金

  1. National Institutes of Health/National Institute of Dental and Craniofacial Research (NIH/NIDCR) [DE027660]
  2. State University of New York at Buffalo, School of Dental Medicine, Department of Oral Biology training grant (NIH/NIDCR) [DE023526]

向作者/读者索取更多资源

This study identified critical enhancers and super-enhancers of the mouse submandibular salivary gland through chromatin immunoprecipitation sequencing experiments. Additionally, it uncovered transcription factors that are likely to play important roles in SMG biology.
The parotid, submandibular, and sublingual glands represent a trio of oral secretory glands whose primary function is to produce saliva, facilitate digestion of food, provide protection against microbes, and maintain oral health. While recent studies have begun to shed light on the global gene expression patterns and profiles of salivary glands, particularly those of mice, relatively little is known about the location and identity of transcriptional control elements. Here we have established the epigenomic landscape of the mouse submandibular salivary gland (SMG) by performing chromatin immunoprecipitation sequencing experiments for 4 key histone marks. Our analysis of the comprehensive SMG data sets and comparisons with those from other adult organs have identified critical enhancers and super-enhancers of the mouse SMG. By further integrating these findings with complementary RNA-sequencing based gene expression data, we have unearthed a number of molecular regulators such as members of the Fox family of transcription factors that are enriched and likely to be functionally relevant for SMG biology. Overall, our studies provide a powerful atlas of cis-regulatory elements that can be leveraged for better understanding the transcriptional control mechanisms of the mouse SMG, discovery of novel genetic switches, and modulating tissue-specific gene expression in a targeted fashion.

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