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Amino Acid Substitutions in the Caenorhabditis elegans RNA Polymerase II Large Subunit AMA-1/RPB-1 that Result in α-Amanitin Resistance and/or Reduced Function
Mutations in the Caenorhabditis elegans RNA polymerase II AMA-1/RPB-1 subunit that cause α-amanitin resistance and/or developmental defects were isolated previously. We identified 12 of these mutations and mapped them onto the Saccharomyces cerevisiae RPB1 structure to provide insight into AMA-1 reg...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Genetics Society of America
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276164/ https://www.ncbi.nlm.nih.gov/pubmed/22384351 http://dx.doi.org/10.1534/g3.111.000968 |
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author | Bowman, Elizabeth Anne Riddle, Donald L. Kelly, William |
author_facet | Bowman, Elizabeth Anne Riddle, Donald L. Kelly, William |
author_sort | Bowman, Elizabeth Anne |
collection | PubMed |
description | Mutations in the Caenorhabditis elegans RNA polymerase II AMA-1/RPB-1 subunit that cause α-amanitin resistance and/or developmental defects were isolated previously. We identified 12 of these mutations and mapped them onto the Saccharomyces cerevisiae RPB1 structure to provide insight into AMA-1 regions that are essential for development in a multicellular organism. |
format | Online Article Text |
id | pubmed-3276164 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Genetics Society of America |
record_format | MEDLINE/PubMed |
spelling | pubmed-32761642012-03-01 Amino Acid Substitutions in the Caenorhabditis elegans RNA Polymerase II Large Subunit AMA-1/RPB-1 that Result in α-Amanitin Resistance and/or Reduced Function Bowman, Elizabeth Anne Riddle, Donald L. Kelly, William G3 (Bethesda) Investigation Mutations in the Caenorhabditis elegans RNA polymerase II AMA-1/RPB-1 subunit that cause α-amanitin resistance and/or developmental defects were isolated previously. We identified 12 of these mutations and mapped them onto the Saccharomyces cerevisiae RPB1 structure to provide insight into AMA-1 regions that are essential for development in a multicellular organism. Genetics Society of America 2011-11-01 /pmc/articles/PMC3276164/ /pubmed/22384351 http://dx.doi.org/10.1534/g3.111.000968 Text en Copyright © 2011 Bowman et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Unported License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Investigation Bowman, Elizabeth Anne Riddle, Donald L. Kelly, William Amino Acid Substitutions in the Caenorhabditis elegans RNA Polymerase II Large Subunit AMA-1/RPB-1 that Result in α-Amanitin Resistance and/or Reduced Function |
title | Amino Acid Substitutions in the Caenorhabditis elegans RNA Polymerase II Large Subunit AMA-1/RPB-1 that Result in α-Amanitin Resistance and/or Reduced Function |
title_full | Amino Acid Substitutions in the Caenorhabditis elegans RNA Polymerase II Large Subunit AMA-1/RPB-1 that Result in α-Amanitin Resistance and/or Reduced Function |
title_fullStr | Amino Acid Substitutions in the Caenorhabditis elegans RNA Polymerase II Large Subunit AMA-1/RPB-1 that Result in α-Amanitin Resistance and/or Reduced Function |
title_full_unstemmed | Amino Acid Substitutions in the Caenorhabditis elegans RNA Polymerase II Large Subunit AMA-1/RPB-1 that Result in α-Amanitin Resistance and/or Reduced Function |
title_short | Amino Acid Substitutions in the Caenorhabditis elegans RNA Polymerase II Large Subunit AMA-1/RPB-1 that Result in α-Amanitin Resistance and/or Reduced Function |
title_sort | amino acid substitutions in the caenorhabditis elegans rna polymerase ii large subunit ama-1/rpb-1 that result in α-amanitin resistance and/or reduced function |
topic | Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276164/ https://www.ncbi.nlm.nih.gov/pubmed/22384351 http://dx.doi.org/10.1534/g3.111.000968 |
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