Searching the Resource Information Network

Our searching services are busy right now. Please try again later

  • Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes
Norway

PMID:17553428  

microRNA modulation of circadian-clock period and entrainment.

Hai-Ying M Cheng | Joseph W Papp | Olga Varlamova | Heather Dziema | Brandon Russell | John P Curfman | Takanobu Nakazawa | Kimiko Shimizu | Hitoshi Okamura | Soren Impey | Karl Obrietan
Neuron | 2007

microRNAs (miRNAs) are a class of small, noncoding RNAs that regulate the stability or translation of mRNA transcripts. Although recent work has implicated miRNAs in development and in disease, the expression and function of miRNAs in the adult mammalian nervous system have not been extensively characterized. Here, we examine the role of two brain-specific miRNAs, miR-219 and miR-132, in modulating the circadian clock located in the suprachiasmatic nucleus. miR-219 is a target of the CLOCK and BMAL1 complex, exhibits robust circadian rhythms of expression, and the in vivo knockdown of miR-219 lengthens the circadian period. miR-132 is induced by photic entrainment cues via a MAPK/CREB-dependent mechanism, modulates clock-gene expression, and attenuates the entraining effects of light. Collectively, these data reveal miRNAs as clock- and light-regulated genes and provide a mechanistic examination of their roles as effectors of pacemaker activity and entrainment.

Pubmed ID: 17553428

Research resources used in this publication

None found

Additional research tools detected in this publication

Antibodies used in this publication

None found

Associated grants

  • Agency: NIMH NIH HHS, United States
    Id: R01 MH062335-05
  • Agency: NINDS NIH HHS, United States
    Id: NS47176
  • Agency: NINDS NIH HHS, United States
    Id: 5P30NS045758
  • Agency: NIMH NIH HHS, United States
    Id: MH64954
  • Agency: NIMH NIH HHS, United States
    Id: MH62335
  • Agency: NINDS NIH HHS, United States
    Id: R01 NS047176-03
  • Agency: NINDS NIH HHS, United States
    Id: P30 NS045758
  • Agency: NIMH NIH HHS, United States
    Id: R01 MH062335-06
  • Agency: NIMH NIH HHS, United States
    Id: R01 MH062335
  • Agency: NINDS NIH HHS, United States
    Id: R01 NS047176
  • Agency: NIMH NIH HHS, United States
    Id: K01 MH064954

Publication data is provided by the National Library of Medicine ® and PubMed ®. Data is retrieved from PubMed ® on a weekly schedule. For terms and conditions see the National Library of Medicine Terms and Conditions.

This is a list of tools and resources that we have found mentioned in this publication.


microRNA.org (tool)

RRID:SCR_006997

Database of microRNA target predictions and expression profiles. Target predictions are based on a development of the miRanda algorithm which incorporates current biological knowledge on target rules and on the use of an up-to-date compendium of mammalian microRNAs. MicroRNA expression profiles are derived from a comprehensive sequencing project of a large set of mammalian tissues and cell lines of normal and disease origin. This website enables users to explore: * The set of genes that are potentially regulated by a particular microRNA. * The implied cooperativity of multiple microRNAs on a particular mRNA. * MicroRNA expression profiles in various mammalian tissues. The web resource provides users with functional information about the growing number of microRNAs and their interaction with target genes in many species and facilitates novel discoveries in microRNA gene regulation. The microRNA Target Detection Software, miRanda, is an algorithm for finding genomic targets for microRNAs. This algorithm has been written in C and is available as an open-source method under the GPL.

View all literature mentions

TargetScan (tool)

RRID:SCR_010845

Web tool to predict biological targets of miRNAs by searching for presence of conserved 8mer, 7mer and 6mer sites that match seed region of each miRNA. Nonconserved sites are also predicted and sites with mismatches in seed region that are compensated by conserved 3' pairing. Used to search for predicted microRNA targets in mammals.

View all literature mentions