Secretory Mechanisms and Dysfunctions Section, National Institute of Dental and Craniofacial Research, National Institutes of Health , Bethesda, Maryland.
Joint Institute for Food Safety and Applied Nutrition, University of Maryland , College Park, Maryland.
Physiol Genomics. 2018 Apr 1;50(4):263-271. doi: 10.1152/physiolgenomics.00124.2017. Epub 2018 Jan 26.
RNA-Seq was used to better understand the molecular nature of the biological differences among the three major exocrine salivary glands in mammals. Transcriptional profiling found that the adult murine parotid, submandibular, and sublingual salivary glands express greater than 14,300 protein-coding genes, and nearly 2,000 of these genes were differentially expressed. Principle component analysis of the differentially expressed genes revealed three distinct clusters according to gland type. The three salivary gland transcriptomes were dominated by a relatively few number of highly expressed genes (6.3%) that accounted for more than 90% of transcriptional output. Of the 912 transcription factors expressed in the major salivary glands, greater than 90% of them were detected in all three glands, while expression for ~2% of them was enriched in an individual gland. Expression of these unique transcription factors correlated with sublingual and parotid specific subsets of both highly expressed and differentially expressed genes. Gene ontology analyses revealed that the highly expressed genes common to all glands were associated with global functions, while many of the genes expressed in a single gland play a major role in the function of that gland. In summary, transcriptional profiling of the three murine major salivary glands identified a limited number of highly expressed genes, differentially expressed genes, and unique transcription factors that represent the transcriptional signatures underlying gland-specific biological properties.
RNA-Seq 被用于更好地理解哺乳动物三种主要外分泌唾液腺之间的生物学差异的分子本质。转录谱分析发现,成年鼠的腮腺、颌下腺和舌下腺表达了超过 14300 个编码蛋白的基因,其中近 2000 个基因的表达存在差异。差异表达基因的主成分分析根据腺体类型揭示了三个明显的簇。这三种唾液腺转录组主要由少数高度表达的基因(6.3%)主导,这些基因占转录输出的 90%以上。在主要唾液腺中表达的 912 个转录因子中,超过 90%的转录因子在所有三个腺体中都被检测到,而约 2%的转录因子在单个腺体中富集。这些独特的转录因子的表达与舌下腺和腮腺特有的高表达和差异表达基因子集相关。基因本体分析表明,所有腺体共有的高度表达基因与全局功能相关,而许多在单个腺体中表达的基因在该腺体的功能中起着主要作用。总之,对三种鼠类主要唾液腺的转录组分析确定了数量有限的高度表达基因、差异表达基因和独特的转录因子,它们代表了腺体特异性生物学特性的转录特征。