A microRNA feedback circuit in midbrain dopamine neurons

被引:947
作者
Kim, Jongpil
Inoue, Keiichi
Ishii, Jennifer
Vanti, William B.
Voronov, Sergey V.
Murchison, Elizabeth
Hannon, Gregory
Abeliovich, Asa
机构
[1] Columbia Univ, Coll Phys & Surg 15 403, Dept Pathol, Ctr Neurobiol & Behav, New York, NY 10032 USA
[2] Columbia Univ, Coll Phys & Surg 15 403, Dept Neurol, Ctr Neurobiol & Behav, New York, NY 10032 USA
[3] Columbia Univ, Coll Phys & Surg 15 403, Taub Inst, New York, NY 10032 USA
[4] Cold Spring Harbor Lab, Watson Sch Biol Sci, Cold Spring Harbor, NY 11724 USA
关键词
D O I
10.1126/science.1140481
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
MicroRNAs ( miRNAs) are evolutionarily conserved, 18- to 25- nucleotide, non-protein coding transcripts that posttranscriptionally regulate gene expression during development. miRNAs also occur in postmitotic cells, such as neurons in the mammalian central nervous system, but their function is less well characterized. We investigated the role of miRNAs in mammalian midbrain dopaminergic neurons ( DNs). We identified a miRNA, miR-133b, that is specifically expressed in midbrain DNs and is deficient in midbrain tissue from patients with Parkinson's disease. miR-133b regulates the maturation and function of midbrain DNs within a negative feedback circuit that includes the paired-like homeodomain transcription factor Pitx3. We propose a role for this feedback circuit in the fine-tuning of dopaminergic behaviors such as locomotion.
引用
收藏
页码:1220 / 1224
页数:5
相关论文
共 16 条
[1]   MicroRNA pathways in flies and worms: Growth, death, fat, stress, and timing [J].
Ambros, V .
CELL, 2003, 113 (06) :673-676
[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]   Engineering stability in gene networks by autoregulation [J].
Becskei, A ;
Serrano, L .
NATURE, 2000, 405 (6786) :590-593
[4]   Dopamine neurons mediate a fast excitatory signal via their glutamatergic synapses [J].
Chuhma, N ;
Zhang, H ;
Masson, J ;
Zhuang, XX ;
Sulzer, D ;
Hen, R ;
Rayport, S .
JOURNAL OF NEUROSCIENCE, 2004, 24 (04) :972-981
[5]   Highly efficient small interfering RNA delivery to primary mammalian neurons induces MicroRNA-like effects before mRNA degradation [J].
Davidson, TJ ;
Harel, S ;
Arboleda, VA ;
Prunell, GF ;
Shelanski, ML ;
Greene, LA ;
Troy, CM .
JOURNAL OF NEUROSCIENCE, 2004, 24 (45) :10040-10046
[6]   Micrornas: Small RNAs with a big role in gene regulation [J].
He, L ;
Hannon, GJ .
NATURE REVIEWS GENETICS, 2004, 5 (07) :522-531
[7]   Selective loss of dopaminergic neurons in the substantia nigra of Pitx3-deficient aphakia mice [J].
Hwang, DY ;
Ardayfio, P ;
Kang, UJ ;
Semina, EV ;
Kim, KS .
MOLECULAR BRAIN RESEARCH, 2003, 114 (02) :123-131
[8]   Human MicroRNA targets [J].
John, B ;
Enright, AJ ;
Aravin, A ;
Tuschl, T ;
Sander, C ;
Marks, DS .
PLOS BIOLOGY, 2004, 2 (11) :1862-1879
[9]   Dopamine neurons derived from embryonic stem cells function in an animal model of Parkinson's disease [J].
Kim, JH ;
Auerbach, JM ;
Rodríguez-Gómez, JA ;
Velasco, I ;
Gavin, D ;
Lumelsky, N ;
Lee, SH ;
Nguyen, J ;
Sánchez-Pernaute, R ;
Bankiewicz, K ;
McKay, R .
NATURE, 2002, 418 (6893) :50-56
[10]   Prediction of mammalian microRNA targets [J].
Lewis, BP ;
Shih, IH ;
Jones-Rhoades, MW ;
Bartel, DP ;
Burge, CB .
CELL, 2003, 115 (07) :787-798