Mach Núria, Berri Mustapha, Esquerré Diane, Chevaleyre Claire, Lemonnier Gaëtan, Billon Yvon, Lepage Patricia, Oswald Isabelle P, Doré Joël, Rogel-Gaillard Claire, Estellé Jordi
UMR1313 Génétique Animale et Biologie Intégrative, INRA, Jouy-en-Josas, France ; UMR1313 Génétique Animale et Biologie Intégrative, AgroParisTech, Jouy-en-Josas, France ; DSV/iRCM/SREIT/LREG, CEA, Jouy-en-Josas, France ; UMR1319 MICALIS, INRA, Jouy-en-Josas, France ; UMR1319 MICALIS, AgroParisTech, Jouy-en-Josas, France.
UMR1282 ISP, INRA, Nouzilly, France ; UMR1282 ISP, Université de Tours, Tours, France.
PLoS One. 2014 Feb 12;9(2):e88515. doi: 10.1371/journal.pone.0088515. eCollection 2014.
The aim of this study was to analyse gene expression along the small intestine (duodenum, jejunum, ileum) and in the ileal Peyer's patches in four young pigs with no clinical signs of disease by transcriptome sequencing. Multidimensional scaling evidenced that samples clustered by tissue type rather than by individual, thus prefiguring a relevant scenario to draw tissue-specific gene expression profiles. Accordingly, 1,349 genes were found differentially expressed between duodenum and jejunum, and up to 3,455 genes between duodenum and ileum. Additionally, a considerable number of differentially expressed genes were found by comparing duodenum (7,027 genes), jejunum (6,122 genes), and ileum (6,991 genes) with ileal Peyer's patches tissue. Functional analyses revealed that most of the significant differentially expressed genes along small intestinal tissues were involved in the regulation of general biological processes such as cell development, signalling, growth and proliferation, death and survival or cell function and maintenance. These results suggest that the intrinsic large turnover of intestinal tissues would have local specificities at duodenum, ileum and jejunum. In addition, in concordance with their biological function, enteric innate immune pathways were overrepresented in ileal Peyer's patches. The reported data provide an expression map of the cell pathway variation in the different small intestinal tissues. Furthermore, expression levels measured in healthy individuals could help to understand changes in gene expression that occur in dysbiosis or pathological states.
本研究的目的是通过转录组测序分析4头无疾病临床症状的幼猪小肠(十二指肠、空肠、回肠)及回肠派尔集合淋巴结中的基因表达情况。多维标度分析表明,样本按组织类型而非个体聚类,从而预示了绘制组织特异性基因表达谱的相关情况。据此,发现十二指肠和空肠之间有1349个基因差异表达,十二指肠和回肠之间多达3455个基因差异表达。此外,通过比较十二指肠(7027个基因)、空肠(6122个基因)、回肠(6991个基因)与回肠派尔集合淋巴结组织,发现了相当数量的差异表达基因。功能分析显示,小肠组织中大多数显著差异表达基因参与一般生物学过程的调控,如细胞发育、信号传导、生长与增殖、死亡与存活或细胞功能与维持。这些结果表明,肠道组织内在的高更新率在十二指肠、回肠和空肠具有局部特异性。此外,与它们的生物学功能一致,肠道固有免疫途径在回肠派尔集合淋巴结中过度表达。所报道的数据提供了不同小肠组织中细胞途径变化的表达图谱。此外,在健康个体中测得的表达水平有助于理解在生态失调或病理状态下发生的基因表达变化。