Global microRNA Expression Profiling of Caenorhabditis elegans Parkinson's Disease Models

被引:98
作者
Asikainen, Suvi [1 ,2 ]
Rudgalvyte, Martina [1 ,2 ]
Heikkinen, Liisa [1 ,2 ]
Louhiranta, Kristiina [1 ,2 ]
Lakso, Merja [1 ,2 ]
Wong, Garry [1 ,2 ]
Nass, Richard [3 ]
机构
[1] Univ Kuopio, Dept Neurobiol, AI Virtanen Inst Mol Sci, FIN-70211 Kuopio, Finland
[2] Univ Kuopio, Dept Biosci, FIN-70211 Kuopio, Finland
[3] Indiana Univ, Dept Pharmacol & Toxicol, Ctr Environm Hlth, Sch Med,Stark Neurosci Res Inst, Indianapolis, IN 46202 USA
关键词
microRNA; Parkinson's disease; Neurodegeneration; Microarray; qRT-PCR; Caenorhabditis elegans; ALPHA-SYNUCLEIN; GENE; RNAS; IDENTIFICATION; MUTATIONS; PATHOLOGY; ENCODES; MIR-84; FAMILY; DJ-1;
D O I
10.1007/s12031-009-9325-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
MicroRNAs (miRNAs) play an important role in human brain development and maintenance. To search for miRNAs that may be involved in the pathogenesis of Parkinsons disease (PD), we utilized miRNA microarrays to identify potential gene expression changes in 115 annotated miRNAs in PD-associated Caenorhabditis elegans models that either overexpress human A53T alpha-synuclein or have mutations within the vesicular catecholamine transporter (cat-1) or parkin (pdr-1) ortholog. Here, we show that 12 specific miRNAs are differentially regulated in the animals overexpressing alpha-synuclein, five in cat-1, and three in the pdr-1 mutants. The family of miR-64 and miR-65 are co-underexpressed in the alpha-synuclein transgenic and cat-1 strains, and members of let-7 family co-underexpressed in the alpha-synuclein and pdr-1 strains; mdl-1 and ptc-1 genes are target candidates for miR-64 and miR-65 and are overexpressed in alpha-synuclein transgenic as well as miR-64/65 (tm3711) knockout animals. These results indicate that miRNAs are differentially expressed in C. elegans PD models and suggest a role for these molecules in disease pathogenesis.
引用
收藏
页码:210 / 218
页数:9
相关论文
共 56 条
[1]
The let-7 microRNA family members mir-48, mir-84, and mir-241 function together to regulate developmental timing in Caenorhabditis elegans [J].
Abbott, AL ;
Alvarez-Saavedra, E ;
Miska, EA ;
Lau, NC ;
Bartel, DP ;
Horvitz, HR ;
Ambros, V .
DEVELOPMENTAL CELL, 2005, 9 (03) :403-414
[2]
The Caenorhabditis elegans hunchback-like gene lin-57/hbl-1 controls developmental time and is regulated by microRNAs [J].
Abrahante, JE ;
Daul, AL ;
Li, M ;
Volk, ML ;
Tennessen, JM ;
Miller, EA ;
Rougvie, AE .
DEVELOPMENTAL CELL, 2003, 4 (05) :625-637
[3]
MicroRNA functions in animal development and human disease [J].
Alvarez-Garcia, I ;
Miska, EA .
DEVELOPMENT, 2005, 132 (21) :4653-4662
[4]
MicroRNAs and other tiny endogenous RNAs in C-elegans [J].
Ambros, V ;
Lee, RC ;
Lavanway, A ;
Williams, PT ;
Jewell, D .
CURRENT BIOLOGY, 2003, 13 (10) :807-818
[5]
Staging of brain pathology related to sporadic Parkinson's disease [J].
Braak, H ;
Del Tredici, K ;
Rüb, U ;
de Vos, RAI ;
Steur, ENHJ ;
Braak, E .
NEUROBIOLOGY OF AGING, 2003, 24 (02) :197-211
[6]
BRENNER S, 1974, GENETICS, V77, P71
[7]
microRNAs as prime players in a combinatorial view of evolution [J].
Cacchiarelli, Davide ;
Santoni, Daniele ;
Bozzoni, Irene .
RNA BIOLOGY, 2008, 5 (03) :120-122
[8]
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
[9]
The cat-1 gene of Caenorhabditis elegans encodes a vesicular monoamine transporter required for specific monoamine-dependent behaviors [J].
Duerr, JS ;
Frisby, DL ;
Gaskin, J ;
Duke, A ;
Asermely, K ;
Huddleston, D ;
Eiden, LE ;
Rand, JB .
JOURNAL OF NEUROSCIENCE, 1999, 19 (01) :72-84
[10]
The genetics of disorders with synuclein pathology and parkinsonism [J].
Farrer, M ;
Gwinn-Hardy, K ;
Hutton, M ;
Hardy, J .
HUMAN MOLECULAR GENETICS, 1999, 8 (10) :1901-1905