1 Adeno-Associated Virus Biology Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USA.
J Dent Res. 2019 Feb;98(2):209-217. doi: 10.1177/0022034518806518. Epub 2018 Nov 4.
Significant effort has been applied to identify the genome-wide gene expression profiles associated with salivary gland development and pathophysiology. However, relatively little is known about the regulators that control salivary gland gene expression. We integrated data from DNase1 digital genomic footprinting, RNA-seq, and gene expression microarrays to comprehensively characterize the cis- and trans-regulatory components controlling gene expression of the healthy submandibular salivary gland. Analysis of 32 human tissues and 87 mouse tissues was performed to identify the highly expressed and tissue-enriched transcription factors driving salivary gland gene expression. Following RNA analysis, protein expression levels and subcellular localization of 39 salivary transcription factors were confirmed by immunohistochemistry. These expression analyses revealed that the salivary gland highly expresses transcription factors associated with endoplasmic reticulum stress, human T-cell lymphotrophic virus 1 expression, and Epstein-Barr virus reactivation. DNase1 digital genomic footprinting to a depth of 333,426,353 reads was performed and utilized to generate a salivary gland gene regulatory network describing the genome-wide chromatin accessibility and transcription factor binding of the salivary gland at a single-nucleotide resolution. Analysis of the DNase1 gene regulatory network identified dense interconnectivity among PLAG1, MYB, and 13 other transcription factors associated with balanced chromosomal translocations and salivary gland tumors. Collectively, these analyses provide a comprehensive atlas of the cis- and trans-regulators of the salivary gland and highlight known aberrantly regulated pathways of diseases affecting the salivary glands.
已经投入了大量的努力来识别与唾液腺发育和病理生理学相关的全基因组基因表达谱。然而,对于控制唾液腺基因表达的调节因子,人们知之甚少。我们整合了来自 DNase1 数字基因组足迹、RNA-seq 和基因表达微阵列的数据,以全面描述控制健康颌下唾液腺基因表达的顺式和反式调控元件。对 32 个人类组织和 87 种小鼠组织进行了分析,以鉴定高度表达和组织富集的转录因子,这些转录因子驱动唾液腺基因表达。进行 RNA 分析后,通过免疫组织化学证实了 39 种唾液腺转录因子的蛋白表达水平和亚细胞定位。这些表达分析表明,唾液腺高度表达与内质网应激、人类 T 细胞白血病病毒 1 表达和 Epstein-Barr 病毒激活相关的转录因子。进行了深度为 333,426,353 个读取的 DNase1 数字基因组足迹分析,并利用该分析生成了唾液腺基因调控网络,该网络描述了唾液腺在单核苷酸分辨率下的全基因组染色质可及性和转录因子结合。DNase1 基因调控网络分析确定了 PLAG1、MYB 和其他 13 个与平衡染色体易位和唾液腺肿瘤相关的转录因子之间的密集相互连接。总之,这些分析提供了唾液腺顺式和反式调控因子的综合图谱,并强调了已知影响唾液腺的疾病的异常调节途径。