LIN-12/Notch Activation Leads to MicroRNA-Mediated Down-Regulation of Vav in C. elegans

Author:

Yoo Andrew S.12,Greenwald Iva12

Affiliation:

1. Integrated Program in Cellular, Molecular, and Biophysical Studies, Howard Hughes Medical Institute, Columbia University College of Physicians and Surgeons, 701 West 168th Street, Room 720, New York, NY 10032, USA.

2. Department of Biochemistry and Molecular Biophysics, Howard Hughes Medical Institute, Columbia University College of Physicians and Surgeons, 701 West 168th Street, Room 720, New York, NY 10032, USA.

Abstract

Cell-cell interactions and cross-talk between signaling pathways specify Caenorhabditis elegans vulval precursor cells (VPCs) to adopt a spatial pattern: a central “1°” VPC, in which epidermal growth factor receptor (EGFR)–mitogen-activated protein kinase (MAPK) activity is high and LIN-12/Notch activity is low, flanked by two “2°” VPCs, in which LIN-12/Notch activity is high and EGFR-MAPK activity is low. Here, we identify a microRNA gene, mir-61 , as a direct transcriptional target of LIN-12 and show that expression of mir-61 promotes the 2° fate. We also identify vav-1 , the ortholog of the Vav oncogene, as a target of mir-61 , and show that down-regulation of VAV-1 promotes lin-12 activity in specifying the 2° fate. Our results suggest that lin-12, mir-61 , and vav-1 form a feedback loop that helps maximize lin-12 activity in the presumptive 2° VPCs.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference29 articles.

1. P. W. Sternberg in WormBook (2005) (www.wormbook.org).

2. I. Greenwald in WormBook (2005) (www.wormbook.org).

3. Crosstalk Between the EGFR and LIN-12/Notch Pathways in C. elegans Vulval Development

4. The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14

5. Supporting Online Material is available on Science Online.

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