Skip to main content
Advertisement

Main menu

  • Home
  • Articles
    • Accepted manuscripts
    • Issue in progress
    • Latest complete issue
    • Issue archive
    • Archive by article type
    • Special issues
    • Subject collections
    • Sign up for alerts
  • About us
    • About Development
    • About the Node
    • Editors and Board
    • Editor biographies
    • Travelling Fellowships
    • Grants and funding
    • Journal Meetings
    • Workshops
    • The Company of Biologists
    • Journal news
  • For authors
    • Submit a manuscript
    • Aims and scope
    • Presubmission enquiries
    • Article types
    • Manuscript preparation
    • Cover suggestions
    • Editorial process
    • Promoting your paper
    • Open Access
    • Biology Open transfer
  • Journal info
    • Journal policies
    • Rights and permissions
    • Media policies
    • Reviewer guide
    • Sign up for alerts
  • Contacts
    • Contacts
    • Subscriptions
    • Feedback
  • COB
    • About The Company of Biologists
    • Development
    • Journal of Cell Science
    • Journal of Experimental Biology
    • Disease Models & Mechanisms
    • Biology Open

User menu

  • Log in
  • Log out

Search

  • Advanced search
Development
  • COB
    • About The Company of Biologists
    • Development
    • Journal of Cell Science
    • Journal of Experimental Biology
    • Disease Models & Mechanisms
    • Biology Open

supporting biologistsinspiring biology

Development

  • Log in
Advanced search

RSS  Twitter  Facebook  YouTube 

  • Home
  • Articles
    • Accepted manuscripts
    • Issue in progress
    • Latest complete issue
    • Issue archive
    • Archive by article type
    • Special issues
    • Subject collections
    • Sign up for alerts
  • About us
    • About Development
    • About the Node
    • Editors and Board
    • Editor biographies
    • Travelling Fellowships
    • Grants and funding
    • Journal Meetings
    • Workshops
    • The Company of Biologists
    • Journal news
  • For authors
    • Submit a manuscript
    • Aims and scope
    • Presubmission enquiries
    • Article types
    • Manuscript preparation
    • Cover suggestions
    • Editorial process
    • Promoting your paper
    • Open Access
    • Biology Open transfer
  • Journal info
    • Journal policies
    • Rights and permissions
    • Media policies
    • Reviewer guide
    • Sign up for alerts
  • Contacts
    • Contacts
    • Subscriptions
    • Feedback
JOURNAL ARTICLES
The terminal differentiation factor LIN-29 is required for proper vulval morphogenesis and egg laying in Caenorhabditis elegans
J.C. Bettinger, S. Euling, A.E. Rougvie
Development 1997 124: 4333-4342;
J.C. Bettinger
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
S. Euling
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
A.E. Rougvie
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • Article
  • Info & metrics
  • PDF
Loading

Summary

Caenorhabditis elegans vulval development culminates during exit from the L4-to-adult molt with the formation of an opening through the adult hypodermis and cuticle that is used for egg laying and mating. Vulva formation requires the heterochronic gene lin-29, which triggers hypodermal cell terminal differentiation during the final molt. lin-29 mutants are unable to lay eggs or mate because no vulval opening forms; instead, a protrusion forms at the site of the vulva. We demonstrate through analysis of genetic mosaics that lin-29 is absolutely required in a small subset of lateral hypodermal seam cells, adjacent to the vulva, for wild-type vulva formation and egg laying. However, lin-29 function is not strictly limited to the lateral hypodermis. First, LIN-29 accumulates in many non-hypodermal cells with known roles in vulva formation or egg laying. Second, animals homozygous for one lin-29 allele, ga94, have the vulval defect and cannot lay eggs, despite having a terminally differentiated adult lateral hypodermis. Finally, vulval morphogenesis and egg laying requires lin-29 activity within the EMS lineage, a lineage that does not generate hypodermal cells.

REFERENCES

    1. Ambros V.
    (1989) A hierarchy of regulatory genes controls a larva-to-adult developmental switch in C. elegans. Cell 57, 49–57
    OpenUrlCrossRefPubMedWeb of Science
    1. Ambros V.,
    2. Horvitz H. R.
    (1984) Heterochronic mutants of the nematode Caenorhabditis elegans. Science 226, 409–16
    OpenUrlAbstract/FREE Full Text
    1. Bettinger J. C.,
    2. Lee K.,
    3. Rougvie A. E.
    (1996) Stage-specificaccumulation of the terminal differentiation factor LIN-29 during C. elegans development. Development 122, 2517–27
    OpenUrlAbstract
    1. Brenner S.
    (1974) The genetics of Caenorhabditis elegans. Genetics 77, 71–94
    OpenUrlAbstract/FREE Full Text
    1. Euling S.,
    2. Ambros V.
    (1996) Heterochronic genes control cell cycle progress and developmental competence of C. elegans vulva precursor cells. Cell 84, 667–676
    OpenUrlCrossRefPubMedWeb of Science
    1. Euling S.,
    2. Ambros V.
    (1996) Reversal of cell fate determination in Caenorhabditis elegans vulval development. Development 122, 2507–2515
    OpenUrlAbstract
    1. Francis G. R.,
    2. Waterston R. H.
    (1991) Muscle cell attachment in Caenorhabditis elegans. J. Cell Biol 114, 465–479
    OpenUrlAbstract/FREE Full Text
    1. Hedgecock E. M.,
    2. Herman R. K.
    (1995) The ncl-1 gene and genetic mosaics of Caenorhabditis elegans. Genetics 141, 989–1006
    OpenUrlAbstract/FREE Full Text
    1. Herman M. A.,
    2. Vassilieva L. L.,
    3. Horvitz H. R.,
    4. Shaw J. E.,
    5. Herman R. K.
    (1995) The C. elegans gene lin-44, which controls the polarity of certain asymmetric cell divisions, encodes a Wnt protein and acts cell nonautonomously. Cell 83, 101–110
    OpenUrlCrossRefPubMedWeb of Science
    1. Herman R. K.,
    2. Hedgecock E. M.
    (1990) Limitation of the size of the vulval primordium of Caenorhabditis elegans by lin-15 expression in surrounding hypodermis. Nature 348, 169–71
    OpenUrlCrossRefPubMed
    1. Hill R. J.,
    2. Sternberg P. W.
    (1992) The lin-3 gene encodes an inductive signal for vulval development in C. elegans. Nature 358, 470–476
    OpenUrlCrossRefPubMedWeb of Science
    1. Kenyon C.
    (1986) A gene involved in the development of the posterior body region of C. elegans. Cell 46, 477–87
    OpenUrlCrossRefPubMedWeb of Science
    1. Kimble J.
    (1981) Alterations in cell lineage following laser ablation of cells in the somatic gonad of Caenorhabditis elegans. Dev. Biol 87, 286–300
    OpenUrlCrossRefPubMedWeb of Science
    1. Kimble J. E.,
    2. White J. G.
    (1981) On the control of germ cell development in Caenorhabditis elegans. Dev. Biol 81, 208–219
    OpenUrlCrossRefPubMedWeb of Science
    1. Lackner M. R.,
    2. Kornfeld K.,
    3. Miller L. M.,
    4. Horvitz H. R.,
    5. Kim S. K.
    (1994) A MAP kinase homolog, mpk-1, is involved in ras -mediated induction of vulval cell fates in Caenorhabditis elegans. Genes Dev 8, 160–173
    OpenUrlAbstract/FREE Full Text
    1. Liu Z.,
    2. Ambros V.
    (1991) Alternative temporal control systems for hypodermal cell differentiation in Caenorhabditis elegans. Nature 350, 162–165
    OpenUrlCrossRef
    1. Liu Z.,
    2. Kirch S.,
    3. Ambros V.
    (1995) The heterochronic gene pathway controls stage-specific transcription of C. elegans collagen genes. Development 121, 2471–2478
    OpenUrlAbstract
    1. Mello C. C.,
    2. Kramer J. M.,
    3. Stinchcomb D.,
    4. Ambros V.
    (1991) Efficient gene transfer in C. elegans: extrachromosomal maintenance and integration of transforming sequences. EMBO J 10, 3959–3970
    OpenUrlPubMedWeb of Science
    1. Miller L. M.,
    2. Waring D. K. K. S.
    (1996). Mosaic analysis using a ncl-1(+) extrachromosomal array reveals that lin-31 acts in the Pn.p cells during Caenorhabditis elegans vulval development. Genetics 143, 1181–1191
    OpenUrlAbstract/FREE Full Text
    1. Newman A. P.,
    2. White J. G.,
    3. Sternberg P. W.
    (1996) Morphogenesis of the C. elegans hermaphrodite uterus. Development 122, 3617–3626
    OpenUrlAbstract
    1. Rougvie A. E.,
    2. Ambros V.
    (1995) The heterochronic gene lin-29 encodes a zinc finger protein that controls a terminal differentiation event in C. elegans. Development 121, 2491–2500
    OpenUrlAbstract
    1. Seydoux G.,
    2. Savage C.,
    3. Greenwald I.
    (1993) Isolation and characterization of mutations causing abnormal eversion of the vulva in Caenorhabditis elegans. Dev. Biol 157, 423–436
    OpenUrlCrossRefPubMedWeb of Science
    1. Sternberg P. W.
    (1988) Lateral inhibition during vulval induction in Caenorhabditis elegans. Nature 335, 551–554
    OpenUrlCrossRefPubMedWeb of Science
    1. Sulston J. E.,
    2. Horvitz H. R.
    (1977) Post-embryonic cell lineages of the nematode, Caenorhabditis elegans. Dev. Biol 56, 110–56
    OpenUrlCrossRefPubMedWeb of Science
    1. White J. G.,
    2. Southgate E.,
    3. Thomson J. N.,
    4. Brenner S.
    (1986) The structure of the nervous system of Caenorhabditis elegans. Philos. Trans. R. Soc. Lond. B Biol. Sci 314, 1–340
    OpenUrlCrossRef
Previous ArticleNext Article
Back to top
Previous ArticleNext Article

This Issue

 Download PDF

Email

Thank you for your interest in spreading the word on Development.

NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address.

Enter multiple addresses on separate lines or separate them with commas.
The terminal differentiation factor LIN-29 is required for proper vulval morphogenesis and egg laying in Caenorhabditis elegans
(Your Name) has sent you a message from Development
(Your Name) thought you would like to see the Development web site.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Share
JOURNAL ARTICLES
The terminal differentiation factor LIN-29 is required for proper vulval morphogenesis and egg laying in Caenorhabditis elegans
J.C. Bettinger, S. Euling, A.E. Rougvie
Development 1997 124: 4333-4342;
del.icio.us logo Digg logo Reddit logo Twitter logo CiteULike logo Facebook logo Google logo Mendeley logo
Citation Tools
JOURNAL ARTICLES
The terminal differentiation factor LIN-29 is required for proper vulval morphogenesis and egg laying in Caenorhabditis elegans
J.C. Bettinger, S. Euling, A.E. Rougvie
Development 1997 124: 4333-4342;

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Alerts

Please log in to add an alert for this article.

Sign in to email alerts with your email address

Article navigation

  • Top
  • Article
  • Info & metrics
  • PDF

Related articles

Cited by...

More in this TOC section

  • REF-1, a protein with two bHLH domains, alters the pattern of cell fusion in C. elegans by regulating Hox protein activity
  • The dermomyotome dorsomedial lip drives growth and morphogenesis of both the primary myotome and dermomyotome epithelium
  • Centrosome migration into the Drosophila oocyte is independent of BicD and egl, and of the organisation of the microtubule cytoskeleton
Show more JOURNAL ARTICLES

Similar articles

Other journals from The Company of Biologists

Journal of Cell Science

Journal of Experimental Biology

Disease Models & Mechanisms

Biology Open

Advertisement

Kathryn Virginia Anderson (1952-2020)

Developmental geneticist Kathryn Anderson passed away at home on 30 November 2020. Tamara Caspary, a former postdoc and friend, remembers Kathryn and her remarkable contribution to developmental biology.


Zooming into 2021

In a new Editorial, Editor-in-Chief James Briscoe and Executive Editor Katherine Brown reflect on the triumphs and tribulations of the last 12 months, and look towards a hopefully calmer and more predictable year.


Read & Publish participation extends worldwide

Over 60 institutions in 12 countries are now participating in our Read & Publish initiative. Here, James Briscoe explains what this means for his institution, The Francis Crick Institute. Find out more and view our full list of participating institutions.


Upcoming special issues

Imaging Development, Stem Cells and Regeneration
Submission deadline: 30 March 2021
Publication: mid-2021

The Immune System in Development and Regeneration
Guest editors: Florent Ginhoux and Paul Martin
Submission deadline: 1 September 2021
Publication: Spring 2022

Both special issues welcome Review articles as well as Research articles, and will be widely promoted online and at key global conferences.


Development presents...

Our successful webinar series continues into 2021, with early-career researchers presenting their papers and a chance to virtually network with the developmental biology community afterwards. Sign up to join our next session:

10 February
Time: 13:00 (GMT)
Chaired by: preLights

Articles

  • Accepted manuscripts
  • Issue in progress
  • Latest complete issue
  • Issue archive
  • Archive by article type
  • Special issues
  • Subject collections
  • Sign up for alerts

About us

  • About Development
  • About the Node
  • Editors and board
  • Editor biographies
  • Travelling Fellowships
  • Grants and funding
  • Journal Meetings
  • Workshops
  • The Company of Biologists

For authors

  • Submit a manuscript
  • Aims and scope
  • Presubmission enquiries
  • Article types
  • Manuscript preparation
  • Cover suggestions
  • Editorial process
  • Promoting your paper
  • Open Access
  • Biology Open transfer

Journal info

  • Journal policies
  • Rights and permissions
  • Media policies
  • Reviewer guide
  • Sign up for alerts

Contact

  • Contact Development
  • Subscriptions
  • Advertising
  • Feedback

 Twitter   YouTube   LinkedIn

© 2021   The Company of Biologists Ltd   Registered Charity 277992