Home LiteratureArticle Details
PMID: 19155321 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Uncoupling of lin-14 mRNA and protein repression by nutrient deprivation in Caenorhabditis elegans.

RNA (New York, N.Y.) ·Vol. 15 ·No. 3 ·2009-03-00 ·Pages 400-5

Holtz J, Pasquinelli AE

Abstract

In animals, microRNAs (miRNAs), typically, pair to sites of partial complementarity in the 3'-untranslated regions (3'UTRs) of target genes. Regulation by miRNAs often results in down-regulation of target mRNA and protein expression by mechanisms that are yet to be fully elucidated. Additionally, changes in environmental conditions have been shown to influence miRNA function in some cell culture systems. Here, we report the effect of nutrient deprivation on regulation of an endogenous miRNA target in developing worms. In Caenorhabditis elegans, the lin-4 miRNA recognizes multiple sites in the lin-14 3'UTR and directs mRNA degradation and translational repression, but it is unclear how these processes are coupled. In this study, we demonstrate that nutrient deprivation results in loss of lin-14 mRNA, but not protein, repression. In worms removed from feeding conditions, lin-14 mRNA reaccumulates despite the continued expression of lin-4 miRNA. The relative increase in lin-14 mRNA levels during nutrient deprivation is less pronounced in genetic mutants lacking lin-4 miRNA or the lin-14 3'UTR target sites. In conclusion, regulation of lin-14 at the mRNA and protein levels can be uncoupled by changes in culture conditions, indicating that miRNA function can be modulated by environment in multicellular organisms. The awareness that endogenous miRNA pathways can be sensitive to environment is an important consideration for elucidating the mechanism used by miRNAs to regulate target mRNA and protein expression.

MeSH Terms
3' Untranslated Regions/metabolism Animals Caenorhabditis elegans/genetics,physiology Caenorhabditis elegans Proteins/genetics,metabolism MicroRNAs/metabolism Nuclear Proteins/genetics,metabolism RNA, Messenger/metabolism
Chemicals
3' Untranslated Regions Caenorhabditis elegans Proteins LIN-14 protein, C elegans MicroRNAs Nuclear Proteins RNA, Messenger lin-4 microRNA, C elegans
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Holtz Janette
Department of Biology, University of California San Diego, La Jolla, California 92093-0349, USA.
Pasquinelli Amy E
References (18)
18 references, click to expand
  1. Two genetic circuits repress the Caenorhabditis elegans heterochronic gene lin-28 after translation initiation.
    Dev Biol. 2002 Mar 15;243(2):215-25 PMID: 11884032
  2. The 21-nucleotide let-7 RNA regulates developmental timing in Caenorhabditis elegans.
    Nature. 2000 Feb 24;403(6772):901-6 PMID: 10706289
  3. The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14.
    Cell. 1993 Dec 3;75(5):843-54 PMID: 8252621
  4. Posttranscriptional regulation of the heterochronic gene lin-14 by lin-4 mediates temporal pattern formation in C. elegans.
    Cell. 1993 Dec 3;75(5):855-62 PMID: 8252622
  5. Insulin and amino-acid regulation of mTOR signaling and kinase activity through the Rheb GTPase.
    Oncogene. 2006 Oct 16;25(48):6361-72 PMID: 17041622
  6. Stress-induced reversal of microRNA repression and mRNA P-body localization in human cells.
    Cold Spring Harb Symp Quant Biol. 2006;71:513-21 PMID: 17381334
  7. Mechanisms of post-transcriptional regulation by microRNAs: are the answers in sight?
    Nat Rev Genet. 2008 Feb;9(2):102-14 PMID: 18197166
  8. Regulation by let-7 and lin-4 miRNAs results in target mRNA degradation.
    Cell. 2005 Aug 26;122(4):553-63 PMID: 16122423
  9. The timing of lin-4 RNA accumulation controls the timing of postembryonic developmental events in Caenorhabditis elegans.
    Dev Biol. 1999 Jun 1;210(1):87-95 PMID: 10364429
  10. A bulged lin-4/lin-14 RNA duplex is sufficient for Caenorhabditis elegans lin-14 temporal gradient formation.
    Genes Dev. 1996 Dec 1;10(23):3041-50 PMID: 8957004
  11. The cold shock domain protein LIN-28 controls developmental timing in C. elegans and is regulated by the lin-4 RNA.
    Cell. 1997 Mar 7;88(5):637-46 PMID: 9054503
  12. Upstream and downstream of mTOR.
    Genes Dev. 2004 Aug 15;18(16):1926-45 PMID: 15314020
  13. The lin-4 regulatory RNA controls developmental timing in Caenorhabditis elegans by blocking LIN-14 protein synthesis after the initiation of translation.
    Dev Biol. 1999 Dec 15;216(2):671-80 PMID: 10642801
  14. Trans-splicing and polyadenylation of let-7 microRNA primary transcripts.
    RNA. 2004 Oct;10(10):1586-94 PMID: 15337850
  15. Expression of the 22 nucleotide let-7 heterochronic RNA throughout the Metazoa: a role in life history evolution?
    Evol Dev. 2003 Jul-Aug;5(4):372-8 PMID: 12823453
  16. Isoform-specific mutations in the Caenorhabditis elegans heterochronic gene lin-14 affect stage-specific patterning.
    Genetics. 2001 Jan;157(1):199-209 PMID: 11139502
  17. Multiple mechanisms are involved in regulating the expression of the developmental timing regulator lin-28 in Caenorhabditis elegans.
    EMBO J. 2006 Dec 13;25(24):5794-804 PMID: 17139256
  18. MicroRNA silencing through RISC recruitment of eIF6.
    Nature. 2007 Jun 14;447(7146):823-8 PMID: 17507929
Article Info
Journal
RNA (New York, N.Y.)
Abbr.
RNA
ISSN
1469-9001
Published
2009-03-00
Epub
2009-00-20
Pages
400-5
Language
English
Region
United States
NLM ID
9509184
PMCID
PMC2657013
Subset
IM
Grants
NIAID NIH HHS · P30 AI036214 · United States
NIGMS NIH HHS · R01 GM071654 · United States
NIGMS NIH HHS · GM071654-01 · United States
NIAID NIH HHS · 5P30 AI36214 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]