Expression profile analysis of microRNA (miRNA) in mouse central nervous system using a new miRNA detection system that examines hybridization signals at every step of washing

被引:69
作者
Hohjoh, Hirohiko
Fukushima, Tatsunobu
机构
[1] Natl Inst Neurosci, NCNP, Tokyo 1878502, Japan
[2] Mitsubishi Rayon Co Ltd, Yokohama Res Labs, Tsurumi Ku, Yokohama, Kanagawa 2300053, Japan
关键词
microRNA; DNA microarray; expression profile; fluorescence; real-time detection; central nervous system; GENES; BRAIN;
D O I
10.1016/j.gene.2006.11.018
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
MicroRNAs (miRNAs) are small noncoding RNAs, with a length of 19 to 23 nucleotides, which appear to be involved in the regulation of gene expression by inhibiting the translation of messenger RNA. Expression profile analysis of miRNAs is necessary to understand their complex role in the regulation of gene expression during the development and differentiation of cells and in various tissues. We describe here a detection system for miRNA expression profiles, using a new type of DNA chip and fluorescent labeled cellular RNAs, which allows real-time detection of hybridization signals at every step of washing and results in highly reproducible miRNA expression profiles. Using the system, we investigated the expression profiles of miRNA in the mouse central nervous system (CNS), namely the spinal cord, medulla oblongata, pons, cerebellum, midbrain, diencephalons, and cerebral hemispheres. The results indicated that although the CNS subregions expressed similar miRNA genes, the expression levels of the miRNAs varied among the subregions, suggesting that the CNS subregions specialized for different functions possess different expression profiles of miRNAs. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:39 / 44
页数:6
相关论文
共 17 条
[1]   Probing microRNAs with microarrays: Tissue specificity and functional inference [J].
Babak, T ;
Zhang, W ;
Morris, Q ;
Blencowe, BJ ;
Hughes, TR .
RNA, 2004, 10 (11) :1813-1819
[2]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[3]   Frequent deletions and down-regulation of micro-RNA genes miR15 and miR16 at 13q14 in chronic lymphocytic leukemia [J].
Calin, GA ;
Dumitru, CD ;
Shimizu, M ;
Bichi, R ;
Zupo, S ;
Noch, E ;
Aldler, H ;
Rattan, S ;
Keating, M ;
Rai, K ;
Rassenti, L ;
Kipps, T ;
Negrini, M ;
Bullrich, F ;
Croce, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (24) :15524-15529
[4]   Antisense inhibition of human miRNAs and indications for an involvement of miRNA in cell growth and apoptosis [J].
Cheng, AM ;
Byrom, MW ;
Shelton, J ;
Ford, LP .
NUCLEIC ACIDS RESEARCH, 2005, 33 (04) :1290-1297
[5]   Processing of primary microRNAs by the Microprocessor complex [J].
Denli, AM ;
Tops, BBJ ;
Plasterk, RHA ;
Ketting, RF ;
Hannon, GJ .
NATURE, 2004, 432 (7014) :231-235
[6]   siRNAs can function as miRNAs [J].
Doench, JG ;
Petersen, CP ;
Sharp, PA .
GENES & DEVELOPMENT, 2003, 17 (04) :438-442
[7]   Accumulation of miR-155 and BIC RNA in human B cell lymphomas [J].
Eis, PS ;
Tam, W ;
Sun, LP ;
Chadburn, A ;
Li, ZD ;
Gomez, MF ;
Lund, E ;
Dahlberg, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (10) :3627-3632
[8]   A microRNA polycistron as a potential human oncogene [J].
He, L ;
Thomson, JM ;
Hemann, MT ;
Hernando-Monge, E ;
Mu, D ;
Goodson, S ;
Powers, S ;
Cordon-Cardo, C ;
Lowe, SW ;
Hannon, GJ ;
Hammond, SM .
NATURE, 2005, 435 (7043) :828-833
[9]   A microRNA in a multiple-turnover RNAi enzyme complex [J].
Hutvágner, G ;
Zamore, PD .
SCIENCE, 2002, 297 (5589) :2056-2060
[10]  
Johnson SM, 2005, CELL, V120, P635, DOI 10.1016/j.cell.2005.01.014