Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.
PLoS One. 2011;6(10):e25997. doi: 10.1371/journal.pone.0025997. Epub 2011 Oct 11.
To investigate the expression of pancreatic microRNAs (miRNAs) during the period of perinatal beta-cell expansion and maturation in rats, determine the localization of these miRNAs and perform a pathway analysis with predicted target mRNAs expressed in perinatal pancreas.
RNA was extracted from whole pancreas at embryonic day 20 (E20), on the day of birth (P0) and two days after birth (P2) and hybridized to miRNA microarrays. Differentially expressed miRNAs were verified by northern blotting and their pancreatic localization determined by in situ hybridization. Pathway analysis was done using regulated sets of mRNAs predicted as targets of the miRNAs. Possible target genes were tested using reporter-gene analysis in INS-1E cells.
Nine miRNAs were differentially expressed perinatally, seven were confirmed to be regulated at the level of the mature miRNA. The localization studies showed endocrine localization of six of these miRNAs (miR-21, -23a, -29a, -125b-5p, -376b-3p and -451), and all were expressed in exocrine cells at one time point at least. Pathways involving metabolic processes, terpenoid and sterol metabolism were selectively affected by concomitant regulation by miRNAs and mRNAs, and Srebf1 was validated as a target of miR-21.
The findings suggest that miRNAs are involved in the functional maturation of pancreatic exocrine and endocrine tissue following birth. Pathway analysis of target genes identify changes in sterol metabolism around birth as being selectively affected by differential miRNA expression during this period.
研究大鼠围产期胰岛β细胞增殖和成熟过程中胰腺 microRNAs(miRNAs)的表达情况,确定这些 miRNAs 的定位,并对围生期胰腺中表达的预测靶 mRNAs 进行途径分析。
从胚胎第 20 天(E20)、出生当天(P0)和出生后两天(P2)的整个胰腺中提取 RNA,并用 miRNA 微阵列进行杂交。通过 northern 印迹验证差异表达的 miRNAs,并通过原位杂交确定其在胰腺中的定位。利用受调控的靶 mRNAs 预测作为 miRNA 靶点的方法进行途径分析。使用 INS-1E 细胞中的报告基因分析测试可能的靶基因。
围生期有 9 个 miRNAs 差异表达,其中 7 个在成熟 miRNA 水平上被证实受到调控。定位研究显示其中 6 个 miRNAs(miR-21、-23a、-29a、-125b-5p、-376b-3p 和 -451)具有内分泌定位,至少有一个在某个时间点在胰腺外分泌细胞中表达。涉及代谢过程、萜类和固醇代谢的途径受到 miRNA 和 mRNAs 同时调节的选择性影响,并且 Srebf1 被验证为 miR-21 的靶基因。
这些发现表明,miRNAs 参与了出生后胰腺外分泌和内分泌组织的功能成熟。靶基因的途径分析表明,出生前后固醇代谢的变化选择性地受到该时期差异表达的 miRNA 的影响。