Home LiteratureArticle Details
PMID: 18334253 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Upregulation of the let-7 microRNA with precocious development in lin-12/Notch hypermorphic Caenorhabditis elegans mutants.

Developmental biology ·Vol. 316 ·No. 2 ·2008-04-15 ·Pages 191-9

Solomon A, Mian Y, Ortega-Cava C, Liu VW, Gurumurthy CB, Naramura M, Band V, Band H

Abstract

The lin-12/Notch signaling pathway is conserved from worms to humans and is a master regulator of metazoan development. Here, we demonstrate that lin-12/Notch gain-of-function (gf) animals display precocious alae at the L4 larval stage with a significant increase in let-7 expression levels. Furthermore, lin-12(gf) animals display a precocious and higher level of let-7 gfp transgene expression in seam cells at L3 stage. Interestingly, lin-12(gf) mutant rescued the lethal phenotype of let-7 mutants similar to other known heterochronic mutants. We propose that lin-12/Notch signaling pathway functions in late developmental timing, upstream of or in parallel to the let-7 heterochronic pathway. Importantly, the human microRNA let-7a was also upregulated in various human cell lines in response to Notch 1 activation, suggesting an evolutionarily conserved cross-talk between let-7 and the canonical lin-12/Notch signaling pathway.

MeSH Terms
Animals Animals, Genetically Modified Blotting, Northern Caenorhabditis elegans/genetics,growth & development Gene Expression Regulation, Developmental Green Fluorescent Proteins/genetics Larva MicroRNAs/genetics Mutation Phenotype Receptors, Notch/genetics Reverse Transcriptase Polymerase Chain Reaction
Chemicals
MicroRNAs Receptors, Notch let-7 microRNA, C elegans Green Fluorescent Proteins
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Solomon Aharon
Division of Molecular Oncology, Evanston Northwestern Healthcare Research Institute, Department of Medicine, Feinberg School of Medicine, USA.
Mian Yousaf
Ortega-Cava Cesar
Liu Victor Won Tat
Gurumurthy Channabasavaiah Basavaraju
Naramura Mayumi
Band Vimla
Band Hamid
References (34)
34 references, click to expand
  1. lag-1, a gene required for lin-12 and glp-1 signaling in Caenorhabditis elegans, is homologous to human CBF1 and Drosophila Su(H).
    Development. 1996 May;122(5):1373-83 PMID: 8625826
  2. RAS is regulated by the let-7 microRNA family.
    Cell. 2005 Mar 11;120(5):635-47 PMID: 15766527
  3. Conservation of the sequence and temporal expression of let-7 heterochronic regulatory RNA.
    Nature. 2000 Nov 2;408(6808):86-9 PMID: 11081512
  4. Notch1 functions as a tumor suppressor in mouse skin.
    Nat Genet. 2003 Mar;33(3):416-21 PMID: 12590261
  5. Molecular mechanisms of developmental timing in C. elegans and Drosophila.
    Dev Cell. 2001 Oct;1(4):453-65 PMID: 11703937
  6. MicroRNAs and their regulatory roles in animals and plants.
    J Cell Physiol. 2007 Feb;210(2):279-89 PMID: 17096367
  7. The heterochronic gene lin-29 encodes a zinc finger protein that controls a terminal differentiation event in Caenorhabditis elegans.
    Development. 1995 Aug;121(8):2491-500 PMID: 7671813
  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. Analysis of gain-of-function mutations of the lin-12 gene of Caenorhabditis elegans.
    Nature. 1990 Jul 12;346(6280):197-9 PMID: 2164160
  10. Activating mutations of NOTCH1 in human T cell acute lymphoblastic leukemia.
    Science. 2004 Oct 8;306(5694):269-71 PMID: 15472075
  11. Aberrant activation of notch signaling in human breast cancer.
    Cancer Res. 2006 Feb 1;66(3):1517-25 PMID: 16452208
  12. The 21-nucleotide let-7 RNA regulates developmental timing in Caenorhabditis elegans.
    Nature. 2000 Feb 24;403(6772):901-6 PMID: 10706289
  13. The C elegans hunchback homolog, hbl-1, controls temporal patterning and is a probable microRNA target.
    Dev Cell. 2003 May;4(5):639-50 PMID: 12737800
  14. The time of appearance of the C. elegans let-7 microRNA is transcriptionally controlled utilizing a temporal regulatory element in its promoter.
    Dev Biol. 2003 Jul 15;259(2):364-79 PMID: 12871707
  15. Reduced expression of the let-7 microRNAs in human lung cancers in association with shortened postoperative survival.
    Cancer Res. 2004 Jun 1;64(11):3753-6 PMID: 15172979
  16. let-7 microRNA functions as a potential growth suppressor in human colon cancer cells.
    Biol Pharm Bull. 2006 May;29(5):903-6 PMID: 16651716
  17. vps25 mosaics display non-autonomous cell survival and overgrowth, and autonomous apoptosis.
    Development. 2006 May;133(10):1871-80 PMID: 16611691
  18. Notch activates sonic hedgehog and both are involved in the specification of dorsal midline cell-fates in Xenopus.
    Development. 2003 May;130(10):2225-38 PMID: 12668635
  19. The mir-84 and let-7 paralogous microRNA genes of Caenorhabditis elegans direct the cessation of molting via the conserved nuclear hormone receptors NHR-23 and NHR-25.
    Development. 2006 Dec;133(23):4631-41 PMID: 17065234
  20. The genetics of Caenorhabditis elegans.
    Genetics. 1974 May;77(1):71-94 PMID: 4366476
  21. Stage-specific accumulation of the terminal differentiation factor LIN-29 during Caenorhabditis elegans development.
    Development. 1996 Aug;122(8):2517-27 PMID: 8756296
  22. Heterochronic mutants of the nematode Caenorhabditis elegans.
    Science. 1984 Oct 26;226(4673):409-16 PMID: 6494891
  23. Heterochronic genes.
    Curr Biol. 2003 Oct 28;13(21):R824-5 PMID: 14588255
  24. Viruses, microRNAs and cancer.
    Oncogene. 2006 Oct 9;25(46):6211-9 PMID: 17028601
  25. Distinctive traits of normal and tumor-derived human mammary epithelial cells expressed in a medium that supports long-term growth of both cell types.
    Proc Natl Acad Sci U S A. 1989 Feb;86(4):1249-53 PMID: 2919173
  26. Spatial and temporal patterns of lin-12 expression during C. elegans hermaphrodite development.
    Genetics. 1995 Oct;141(2):513-26 PMID: 8647389
  27. 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
  28. The lin-41 RBCC gene acts in the C. elegans heterochronic pathway between the let-7 regulatory RNA and the LIN-29 transcription factor.
    Mol Cell. 2000 Apr;5(4):659-69 PMID: 10882102
  29. Reciprocal changes in expression of the receptor lin-12 and its ligand lag-2 prior to commitment in a C. elegans cell fate decision.
    Cell. 1994 Dec 30;79(7):1187-98 PMID: 8001154
  30. The Caenorhabditis elegans heterochronic gene pathway controls stage-specific transcription of collagen genes.
    Development. 1995 Aug;121(8):2471-8 PMID: 7671811
  31. Notch signalling: a simple pathway becomes complex.
    Nat Rev Mol Cell Biol. 2006 Sep;7(9):678-89 PMID: 16921404
  32. Production of high-titer helper-free retroviruses by transient transfection.
    Proc Natl Acad Sci U S A. 1993 Sep 15;90(18):8392-6 PMID: 7690960
  33. Regulation of a senescence checkpoint response by the E2F1 transcription factor and p14(ARF) tumor suppressor.
    Mol Cell Biol. 2000 Jan;20(1):273-85 PMID: 10594030
  34. LIN-12/Notch signaling: lessons from worms and flies.
    Genes Dev. 1998 Jun 15;12(12):1751-62 PMID: 9637676
Article Info
Journal
Developmental biology
Abbr.
Dev Biol
ISSN
1095-564X
Published
2008-04-15
Epub
2008-00-11
Pages
191-9
Language
English
Region
United States
NLM ID
0372762
PMCID
PMC2390880
Subset
IM
Grants
NCI NIH HHS · 1U54 CA119341-01 · United States
NCI NIH HHS · R01 CA105489-05 · United States
NCI NIH HHS · R01 CA087986-09 · United States
NCI NIH HHS · R01 CA105489-03 · United States
NCI NIH HHS · R01 CA116552-01A2 · United States
NCI NIH HHS · CA94143 · United States
NCI NIH HHS · R01 CA116552-02 · United States
NCI NIH HHS · R01 CA099163-05 · United States
NCI NIH HHS · R01 CA087986-10 · United States
NCI NIH HHS · CA87986 · United States
NCI NIH HHS · R01 CA087986 · United States
NCI NIH HHS · R01 CA099900-05 · United States
NCI NIH HHS · R01 CA099163-04 · United States
NCI NIH HHS · R01 CA087986-08 · United States
NCI NIH HHS · R01 CA096844 · United States
NCI NIH HHS · CA96844 · United States
NCI NIH HHS · R01 CA099900-07 · United States
NCI NIH HHS · CA81076 · United States
NCI NIH HHS · R01 CA099900-06 · United States
NCI NIH HHS · R01 CA094143 · United States
NCI NIH HHS · CA116552 · United States
NCI NIH HHS · R01 CA099163-07 · United States
NCI NIH HHS · R01 CA116552 · United States
NCI NIH HHS · R01 CA105489 · United States
NCI NIH HHS · R01 CA087986-11 · United States
NCI NIH HHS · U54 CA119341 · United States
NCI NIH HHS · R01 CA099163-06 · United States
NCI NIH HHS · CA99163 · United States
NCI NIH HHS · R01 CA105489-04 · United States
NCI NIH HHS · CA76118 · United States
NCI NIH HHS · R01 CA099900 · United States
NCI NIH HHS · R01 CA081076 · United States
NCI NIH HHS · R01 CA099163 · United States
NCI NIH HHS · R01 CA087986-07 · United States
NCI NIH HHS · R01 CA105489-06 · United States
NCI NIH HHS · CA99900 · 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: product@genelibs.com