Literature DB >> 16806150

Novel gain-of-function alleles demonstrate a role for the heterochronic gene lin-41 in C. elegans male tail tip morphogenesis.

Tania Del Rio-Albrechtsen1, Karin Kiontke, Shu-Yi Chiou, David H A Fitch.   

Abstract

To gain an understanding of the genes and mechanisms that govern morphogenesis and its evolution, we have analyzed mutations that disrupt this process in a simple model structure, the male tail tip of the rhabditid nematode C. elegans. During the evolution of rhabditid male tails, there have been several independent changes from tails with rounded tips ("peloderan", as in C. elegans) to those with pointed tips ("leptoderan"). Mutations which produce leptoderan (Lep) tails in C. elegans thus identify candidate genes and pathways in which evolutionary changes could have produced leptoderan tails from peloderan ancestors. Here we report that two novel, gain-of-function (gf) alleles of lin-41 have lesions predicted to affect the N-terminus of the RBCC-domain LIN-41 protein. Both gf alleles cause the tail tip of adult males to retain the pointed shape of the juvenile tails, producing a Lep phenotype that looks like the tails of leptoderan species. Consistent with its role in the heterochronic pathway, we find that lin-41 governs the timing and extent of male tail tip morphogenesis in a dose-dependent manner. Specifically, the Lep phenotype results from a heterochronic delay in the retraction and fusion of the tail tip cells during L4 morphogenesis, such that retraction is not completed before the adult molt. Conversely, we find that tail tip morphogenesis and cell fusions begin precociously at the L3 stage in the reduced-function lin-41 mutant, ma104, resulting in over-retracted male tails in the adult. Because modulated anti-LIN-41 RNAi knockdowns in the gf mutants restore wild-type phenotype, we suggest that the leptoderan phenotype of the gf alleles is due to a higher activity of otherwise normal LIN-41. Additionally, the gf allele is suppressed by the wild-type allele, suggesting that LIN-41 normally regulates itself, possibly by autoubiquitination. We speculate that small changes affecting LIN-41 could have been significant for male tail evolution.

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Year:  2006        PMID: 16806150     DOI: 10.1016/j.ydbio.2006.04.472

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  16 in total

Review 1.  Non-neuronal cell outgrowth in C. elegans.

Authors:  Srimoyee Ghosh; Sylvia A Vetrone; Paul W Sternberg
Journal:  Worm       Date:  2017-11-14

2.  The Long Non-Coding RNA lep-5 Promotes the Juvenile-to-Adult Transition by Destabilizing LIN-28.

Authors:  Karin C Kiontke; R Antonio Herrera; Edward Vuong; Jintao Luo; Erich M Schwarz; David H A Fitch; Douglas S Portman
Journal:  Dev Cell       Date:  2019-04-04       Impact factor: 12.270

3.  Expressing and characterization of mLIN-41 in mouse early embryos and adult muscle tissues.

Authors:  Gang Yu; Yurong Yang; Guimei Tian
Journal:  J Mol Histol       Date:  2010-09-08       Impact factor: 2.611

4.  Makorin ortholog LEP-2 regulates LIN-28 stability to promote the juvenile-to-adult transition in Caenorhabditis elegans.

Authors:  R Antonio Herrera; Karin Kiontke; David H A Fitch
Journal:  Development       Date:  2016-01-25       Impact factor: 6.868

Review 5.  LIN-41/TRIM71: emancipation of a miRNA target.

Authors:  Matyas Ecsedi; Helge Grosshans
Journal:  Genes Dev       Date:  2013-03-15       Impact factor: 11.361

6.  A bow-tie genetic architecture for morphogenesis suggested by a genome-wide RNAi screen in Caenorhabditis elegans.

Authors:  Matthew D Nelson; Elinor Zhou; Karin Kiontke; Hélène Fradin; Grayson Maldonado; Daniel Martin; Khushbu Shah; David H A Fitch
Journal:  PLoS Genet       Date:  2011-03-03       Impact factor: 5.917

7.  lin-28 controls the succession of cell fate choices via two distinct activities.

Authors:  Bhaskar Vadla; Kevin Kemper; Jennifer Alaimo; Christian Heine; Eric G Moss
Journal:  PLoS Genet       Date:  2012-03-22       Impact factor: 5.917

8.  The TRIM-NHL protein LIN-41 and the OMA RNA-binding proteins antagonistically control the prophase-to-metaphase transition and growth of Caenorhabditis elegans oocytes.

Authors:  Caroline A Spike; Donna Coetzee; Carly Eichten; Xin Wang; Dave Hansen; David Greenstein
Journal:  Genetics       Date:  2014-09-26       Impact factor: 4.562

9.  E1 ubiquitin-activating enzyme UBA-1 plays multiple roles throughout C. elegans development.

Authors:  Madhura Kulkarni; Harold E Smith
Journal:  PLoS Genet       Date:  2008-07-18       Impact factor: 5.917

10.  RACK-1 regulates let-7 microRNA expression and terminal cell differentiation in Caenorhabditis elegans.

Authors:  Yu-De Chu; Wei-Chieh Wang; Shi-An A Chen; Yen-Ting Hsu; Meng-Wei Yeh; Frank J Slack; Shih-Peng Chan
Journal:  Cell Cycle       Date:  2014-04-28       Impact factor: 4.534

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