MicroRNAs of rat articular cartilage at different developmental stages identified by Solexa sequencing

被引:34
作者
Sun, J. [1 ,2 ]
Zhong, N. [1 ,2 ]
Li, Q. [3 ]
Min, Z. [1 ,2 ]
Zhao, W. [1 ,2 ]
Sun, Q. [1 ,2 ]
Tian, L. [1 ,2 ]
Yu, H. [1 ,2 ]
Shi, Q. [1 ,2 ]
Zhang, F. [1 ,2 ]
Lu, S. [1 ,2 ,4 ]
机构
[1] Xi An Jiao Tong Univ, Dept Genet & Mol Biol, Coll Med, Xian 710061, Shaanxi, Peoples R China
[2] Xi An Jiao Tong Univ, Minist Educ, Key Lab Environm & Genes Related Dis, Xian 710061, Shaanxi, Peoples R China
[3] Beijing Genom Inst, Shenzhen 518083, Peoples R China
[4] Xi An Jiao Tong Univ, Dept Epidemiol & Hlth Stat, Sch Publ Hlth, Coll Med, Xian 710061, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
MicroRNAs; Solexa sequencing; Articular cartilage development; OSTEOBLAST DIFFERENTIATION; STEM-CELLS; EXPRESSION; MODEL; BONE;
D O I
10.1016/j.joca.2011.07.002
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Background: Expression profiles of microRNAs (miRNAs) can shape the repertoire of proteins expressed in development, differentiation and diseases. This study aimed to identify miRNA profile of articular cartilage at different developmental stages in rats. Methods: Three small RNA libraries were constructed from the femoral head cartilage of Sprague-Dawley (SD) rats at postnatal day 0, day 21 and day 42 and sequenced by a deep sequencing approach. Then a bioinformatics approach was employed to distinguish genuine miRNAs from small RNAs represented in the mass sequencing data. The expression of indicated miRNAs was determined by stem-loop RT-qPCR to valuate the consistency with Solexa sequencing. Results: Two hundred and fifty-eight of 310 known miRNA and miRNA* genes were organized into 91 compact clusters. Two hundred and forty-six miRNAs were detected in all three small RNA libraries of rat articular cartilage. Forty-six, fifty-two and fifty-six miRNA* genes were identified from three small RNA libraries, respectively, and 86 novel miRNA candidate genes were found simultaneously. In addition, 23 known miRNAs were up-regulated (fold change >= 4); six were down-regulated (fold change <= -4) during articular cartilage development. The predicted targets of differentially expressed miRNAs were locally secreted factors and transcription factors that regulate proliferation and differentiation of chondrocytes. The same expression tendency of indicated miRNAs during articular cartilage development stages was observed by using Solexa sequencing and stem-loop RT-qPCR. Conclusion: Our study provided a unique opportunity to decipher how the elaboration of the miRNA repertoire contributes to the development process of articular cartilage. (C) 2011 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1237 / 1245
页数:9
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