期刊文献+

MicroRNA-29a modulates axon branching by targeting doublecortin in primary neurons 被引量:2

MicroRNA-29a modulates axon branching by targeting doublecortin in primary neurons
原文传递
导出
摘要 MicroRNAs (miRNAs) are endogenously expressed small, non-coding transcripts that regulate protein expression. Substantial evidences suggest that miRNAs are enriched in central nervous system, where they are hypothesized to play pivotal roles during neural devel- opment. In the present study, we analyzed miRNAs expression in mice cerebral cortex and hippocampus at different developmental stages and found miR-29a increased dramatically at postnatal stages. In addition, we provided strong evidences that miR-29a is enriched in mature neurons both in vitro and in v/vo. Further investigation demonstrated that the activation of gluta- mate receptors induced endogenous miR-29a level in primary neurons. Moreover, we showed that miR-29a directly regulated its target protein Doublecortin (DCX) expression, which further modulated axon branching in primary culture. Together, our results suggested that miR-29a play an important role in neuronal development of mice cerebrum. MicroRNAs (miRNAs) are endogenously expressed small, non-coding transcripts that regulate protein expression. Substantial evidences suggest that miRNAs are enriched in central nervous system, where they are hypothesized to play pivotal roles during neural devel- opment. In the present study, we analyzed miRNAs expression in mice cerebral cortex and hippocampus at different developmental stages and found miR-29a increased dramatically at postnatal stages. In addition, we provided strong evidences that miR-29a is enriched in mature neurons both in vitro and in v/vo. Further investigation demonstrated that the activation of gluta- mate receptors induced endogenous miR-29a level in primary neurons. Moreover, we showed that miR-29a directly regulated its target protein Doublecortin (DCX) expression, which further modulated axon branching in primary culture. Together, our results suggested that miR-29a play an important role in neuronal development of mice cerebrum.
出处 《Protein & Cell》 SCIE CAS CSCD 2014年第2期160-169,共10页 蛋白质与细胞(英文版)
基金 This work was supported by grants from the National Natural Science Foundation of China (Grant Nos. 31000478, 31100777 and 31271378).
关键词 MiRNAs are approximately 21 nucleotide non-codingtranscripts that are derived from hairpin precursors which MiRNAs are approximately 21 nucleotide non-codingtranscripts that are derived from hairpin precursors, which
  • 相关文献

同被引文献20

  • 1Barrel D P. MieroRNAs: genomics, biogenesis, mechanism, and func- tion[J], cell, 2004, 116(2): 281-297.
  • 2Huang Y, Shen X J, Zou Q, et al. Biological functions of microRNAs: a review [J]. Journal of physiology and biochemistry, 2011, 67(1): 129-139.
  • 3Deng C X. The Use of Cre-loxP Technology and Inducible Systems to Generate Mouse Models of Cancer[M]. Genetically Engineered Mice for Cancer Research. Springer New York, 2012:17-36.
  • 4Horvath P, Barrengou R. CRISPR/Cas, the immune system of bacteria and archnea[J]. Science, 2010, 327(5962): 167-170.
  • 5Gaj T, Gersbach C A, Barbas C F. ZFN, TALEN, and CRISPR/Cas- based methods for genome engineering [J]. Trends in bioteehnology, 2013, 31(7): 397-405.
  • 6Hsu P D, Lander E S, Zhang F. Development and applications of CRISPR-Cas9 for genome engineering [J]. Cell, 2014, 157 (6): 1262-1278.
  • 7Wu Y, Liang D, Wang Y, et al. Correction of a genetic disease in mouse via use of CRISPR-Cas9 [J]. Cell stem cell, 2013, 13 (6): 659-662.
  • 8Van Tongelen A, Loriot A, De Backer O, et al. Application of CRISPR/eas9-Direeted Homologous Recombination to the Genera- tion of Human Tumor Cells with Conditional Knockout of an X-Linked MieroRNA Locus [J]. Gene Technology, 2015, 4 (2): e1000124.
  • 9Han J, Zhang J, Chert L, et al. Efficient in vivo deletion of a large im- printed IncRNA by CRISPR/Cas9 [J]. RNA biology, 2014, 11 (7): 829-835.
  • 10Sander J D, Joung J K. CRISPR-Cas systems for editing, regulating and targeting genomes [J]. Nature bioteclmology, 2014, 32 (4): 347-355.

引证文献2

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部