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LET-99 inhibits lateral posterior pulling forces during asymmetric spindle elongation in C. elegans embryos
Cortical pulling on astral microtubules positions the mitotic spindle in response to PAR polarity cues and G protein signaling in many systems. In Caenorhabditis elegans single-cell embryos, posterior spindle displacement depends on Gα and its regulators GPR-1/2 and LIN-5. GPR-1/2 and LIN-5 are nece...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2867312/ https://www.ncbi.nlm.nih.gov/pubmed/20421425 http://dx.doi.org/10.1083/jcb.201001115 |
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author | Krueger, Lori E. Wu, Jui-Ching Tsou, Meng-Fu Bryan Rose, Lesilee S. |
author_facet | Krueger, Lori E. Wu, Jui-Ching Tsou, Meng-Fu Bryan Rose, Lesilee S. |
author_sort | Krueger, Lori E. |
collection | PubMed |
description | Cortical pulling on astral microtubules positions the mitotic spindle in response to PAR polarity cues and G protein signaling in many systems. In Caenorhabditis elegans single-cell embryos, posterior spindle displacement depends on Gα and its regulators GPR-1/2 and LIN-5. GPR-1/2 and LIN-5 are necessary for cortical pulling forces and become enriched at the posterior cortex, which suggests that higher forces act on the posterior spindle pole compared with the anterior pole. However, the precise distribution of cortical forces and how they are regulated remains to be determined. Using spindle severing, single centrosome assays, and centrosome fragmentation, we show that both the anterior and posterior cortices generate more pulling force than the lateral–posterior region. Lateral inhibition depends on LET-99, which inhibits GPR-1/2 localization to produce a bipolar GPR-1/2 pattern. Thus, rather than two domains of cortical force, there are three. We propose that the attenuation of lateral forces prevents counterproductive pulling, resulting in a higher net force toward the posterior that contributes to spindle elongation and displacement. |
format | Text |
id | pubmed-2867312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-28673122010-11-03 LET-99 inhibits lateral posterior pulling forces during asymmetric spindle elongation in C. elegans embryos Krueger, Lori E. Wu, Jui-Ching Tsou, Meng-Fu Bryan Rose, Lesilee S. J Cell Biol Research Articles Cortical pulling on astral microtubules positions the mitotic spindle in response to PAR polarity cues and G protein signaling in many systems. In Caenorhabditis elegans single-cell embryos, posterior spindle displacement depends on Gα and its regulators GPR-1/2 and LIN-5. GPR-1/2 and LIN-5 are necessary for cortical pulling forces and become enriched at the posterior cortex, which suggests that higher forces act on the posterior spindle pole compared with the anterior pole. However, the precise distribution of cortical forces and how they are regulated remains to be determined. Using spindle severing, single centrosome assays, and centrosome fragmentation, we show that both the anterior and posterior cortices generate more pulling force than the lateral–posterior region. Lateral inhibition depends on LET-99, which inhibits GPR-1/2 localization to produce a bipolar GPR-1/2 pattern. Thus, rather than two domains of cortical force, there are three. We propose that the attenuation of lateral forces prevents counterproductive pulling, resulting in a higher net force toward the posterior that contributes to spindle elongation and displacement. The Rockefeller University Press 2010-05-03 /pmc/articles/PMC2867312/ /pubmed/20421425 http://dx.doi.org/10.1083/jcb.201001115 Text en © 2010 Krueger et al. 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 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Krueger, Lori E. Wu, Jui-Ching Tsou, Meng-Fu Bryan Rose, Lesilee S. LET-99 inhibits lateral posterior pulling forces during asymmetric spindle elongation in C. elegans embryos |
title | LET-99 inhibits lateral posterior pulling forces during asymmetric spindle elongation in C. elegans embryos |
title_full | LET-99 inhibits lateral posterior pulling forces during asymmetric spindle elongation in C. elegans embryos |
title_fullStr | LET-99 inhibits lateral posterior pulling forces during asymmetric spindle elongation in C. elegans embryos |
title_full_unstemmed | LET-99 inhibits lateral posterior pulling forces during asymmetric spindle elongation in C. elegans embryos |
title_short | LET-99 inhibits lateral posterior pulling forces during asymmetric spindle elongation in C. elegans embryos |
title_sort | let-99 inhibits lateral posterior pulling forces during asymmetric spindle elongation in c. elegans embryos |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2867312/ https://www.ncbi.nlm.nih.gov/pubmed/20421425 http://dx.doi.org/10.1083/jcb.201001115 |
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