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Metaphase to Anaphase (mat) Transition–Defective Mutants inCaenorhabditis elegans
The metaphase to anaphase transition is a critical stage of the eukaryotic cell cycle, and, thus, it is highly regulated. Errors during this transition can lead to chromosome segregation defects and death of the organism. In genetic screens for temperature-sensitive maternal effect embryonic lethal...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2000
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2150685/ https://www.ncbi.nlm.nih.gov/pubmed/11134076 |
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author | Golden, Andy Sadler, Penny L. Wallenfang, Matthew R. Schumacher, Jill M. Hamill, Danielle R. Bates, Gayle Bowerman, Bruce Seydoux, Geraldine Shakes, Diane C. |
author_facet | Golden, Andy Sadler, Penny L. Wallenfang, Matthew R. Schumacher, Jill M. Hamill, Danielle R. Bates, Gayle Bowerman, Bruce Seydoux, Geraldine Shakes, Diane C. |
author_sort | Golden, Andy |
collection | PubMed |
description | The metaphase to anaphase transition is a critical stage of the eukaryotic cell cycle, and, thus, it is highly regulated. Errors during this transition can lead to chromosome segregation defects and death of the organism. In genetic screens for temperature-sensitive maternal effect embryonic lethal (Mel) mutants, we have identified 32 mutants in the nematode Caenorhabditis elegans in which fertilized embryos arrest as one-cell embryos. In these mutant embryos, the oocyte chromosomes arrest in metaphase of meiosis I without transitioning to anaphase or producing polar bodies. An additional block in M phase exit is evidenced by the failure to form pronuclei and the persistence of phosphohistone H3 and MPM-2 antibody staining. Spermatocyte meiosis is also perturbed; primary spermatocytes arrest in metaphase of meiosis I and fail to produce secondary spermatocytes. Analogous mitotic defects cause M phase delays in mitotic germline proliferation. We have named this class of mutants “mat” for metaphase to anaphase transition defective. These mutants, representing six different complementation groups, all map near genes that encode subunits of the anaphase promoting complex or cyclosome, and, here, we show that one of the genes, emb-27, encodes the C. elegans CDC16 ortholog. |
format | Text |
id | pubmed-2150685 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21506852008-05-01 Metaphase to Anaphase (mat) Transition–Defective Mutants inCaenorhabditis elegans Golden, Andy Sadler, Penny L. Wallenfang, Matthew R. Schumacher, Jill M. Hamill, Danielle R. Bates, Gayle Bowerman, Bruce Seydoux, Geraldine Shakes, Diane C. J Cell Biol Original Article The metaphase to anaphase transition is a critical stage of the eukaryotic cell cycle, and, thus, it is highly regulated. Errors during this transition can lead to chromosome segregation defects and death of the organism. In genetic screens for temperature-sensitive maternal effect embryonic lethal (Mel) mutants, we have identified 32 mutants in the nematode Caenorhabditis elegans in which fertilized embryos arrest as one-cell embryos. In these mutant embryos, the oocyte chromosomes arrest in metaphase of meiosis I without transitioning to anaphase or producing polar bodies. An additional block in M phase exit is evidenced by the failure to form pronuclei and the persistence of phosphohistone H3 and MPM-2 antibody staining. Spermatocyte meiosis is also perturbed; primary spermatocytes arrest in metaphase of meiosis I and fail to produce secondary spermatocytes. Analogous mitotic defects cause M phase delays in mitotic germline proliferation. We have named this class of mutants “mat” for metaphase to anaphase transition defective. These mutants, representing six different complementation groups, all map near genes that encode subunits of the anaphase promoting complex or cyclosome, and, here, we show that one of the genes, emb-27, encodes the C. elegans CDC16 ortholog. The Rockefeller University Press 2000-12-25 /pmc/articles/PMC2150685/ /pubmed/11134076 Text en © 2000 Government This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Original Article Golden, Andy Sadler, Penny L. Wallenfang, Matthew R. Schumacher, Jill M. Hamill, Danielle R. Bates, Gayle Bowerman, Bruce Seydoux, Geraldine Shakes, Diane C. Metaphase to Anaphase (mat) Transition–Defective Mutants inCaenorhabditis elegans |
title | Metaphase to Anaphase (mat) Transition–Defective Mutants inCaenorhabditis elegans
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title_full | Metaphase to Anaphase (mat) Transition–Defective Mutants inCaenorhabditis elegans
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title_fullStr | Metaphase to Anaphase (mat) Transition–Defective Mutants inCaenorhabditis elegans
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title_full_unstemmed | Metaphase to Anaphase (mat) Transition–Defective Mutants inCaenorhabditis elegans
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title_short | Metaphase to Anaphase (mat) Transition–Defective Mutants inCaenorhabditis elegans
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title_sort | metaphase to anaphase (mat) transition–defective mutants incaenorhabditis elegans |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2150685/ https://www.ncbi.nlm.nih.gov/pubmed/11134076 |
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