Literature DB >> 12736204

The C. elegans LIM homeobox gene lin-11 specifies multiple cell fates during vulval development.

Bhagwati P Gupta1, Minqin Wang, Paul W Sternberg.   

Abstract

LIM homeobox family members regulate a variety of cell fate choices during animal development. In C. elegans, mutations in the LIM homeobox gene lin-11 have previously been shown to alter the cell division pattern of a subset of the 2 degrees lineage vulval cells. We demonstrate multiple functions of lin-11 during vulval development. We examined the fate of vulval cells in lin-11 mutant animals using five cellular markers and found that lin-11 is necessary for the patterning of both 1 degrees and 2 degrees lineage cells. In the absence of lin-11 function, vulval cells fail to acquire correct identity and inappropriately fuse with each other. The expression pattern of lin-11 reveals dynamic changes during development. Using a temporally controlled overexpression system, we show that lin-11 is initially required in vulval cells for establishing the correct invagination pattern. This process involves asymmetric expression of lin-11 in the 2 degrees lineage cells. Using a conditional RNAi approach, we show that lin-11 regulates vulval morphogenesis. Finally, we show that LDB-1, a NLI/Ldb1/CLIM2 family member, interacts physically with LIN-11, and is necessary for vulval morphogenesis. Together, these findings demonstrate that temporal regulation of lin-11 is crucial for the wild-type vulval patterning.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12736204     DOI: 10.1242/dev.00500

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  20 in total

1.  Transcriptional network underlying Caenorhabditis elegans vulval development.

Authors:  Takao Inoue; Minqin Wang; Ted O Ririe; Jolene S Fernandes; Paul W Sternberg
Journal:  Proc Natl Acad Sci U S A       Date:  2005-03-04       Impact factor: 11.205

2.  Rapid sequence evolution of transcription factors controlling neuron differentiation in Caenorhabditis.

Authors:  Richard Jovelin
Journal:  Mol Biol Evol       Date:  2009-07-09       Impact factor: 16.240

3.  The C. elegans homolog of the mammalian tumor suppressor Dep-1/Scc1 inhibits EGFR signaling to regulate binary cell fate decisions.

Authors:  Thomas A Berset; Erika Fröhli Hoier; Alex Hajnal
Journal:  Genes Dev       Date:  2005-05-18       Impact factor: 11.361

4.  A Wnt-Frz/Ror-Dsh pathway regulates neurite outgrowth in Caenorhabditis elegans.

Authors:  Song Song; Bo Zhang; Hui Sun; Xia Li; Yanhui Xiang; Zhonghua Liu; Xun Huang; Mei Ding
Journal:  PLoS Genet       Date:  2010-08-12       Impact factor: 5.917

5.  The small ubiquitin-like modifier (SUMO) is required for gonadal and uterine-vulval morphogenesis in Caenorhabditis elegans.

Authors:  Limor Broday; Irina Kolotuev; Christine Didier; Anindita Bhoumik; Bhagwati P Gupta; Paul W Sternberg; Benjamin Podbilewicz; Ze'ev Ronai
Journal:  Genes Dev       Date:  2004-10-01       Impact factor: 11.361

Review 6.  LIM-domain-binding protein 1: a multifunctional cofactor that interacts with diverse proteins.

Authors:  Jacqueline M Matthews; Jane E Visvader
Journal:  EMBO Rep       Date:  2003-12       Impact factor: 8.807

7.  Re-programming of C. elegans male epidermal precursor fates by Wnt, Hox, and LIN-12/Notch activities.

Authors:  Hui Yu; Adeline Seah; Paul W Sternberg
Journal:  Dev Biol       Date:  2010-05-15       Impact factor: 3.582

8.  Using Caenorhabditis elegans as a model organism for evaluating extracellular signal-regulated kinase docking domain inhibitors.

Authors:  Fengming Chen; Alexander D Mackerell; Yuan Luo; Paul Shapiro
Journal:  J Cell Commun Signal       Date:  2008-12-23       Impact factor: 5.782

9.  Wnt and EGF pathways act together to induce C. elegans male hook development.

Authors:  Hui Yu; Adeline Seah; Michael A Herman; Edwin L Ferguson; H Robert Horvitz; Paul W Sternberg
Journal:  Dev Biol       Date:  2008-12-30       Impact factor: 3.582

10.  C. elegans BED domain transcription factor BED-3 controls lineage-specific cell proliferation during organogenesis.

Authors:  Takao Inoue; Paul W Sternberg
Journal:  Dev Biol       Date:  2009-12-21       Impact factor: 3.582

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.