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Genome-Wide Reverse Genetics Framework to Identify Novel Functions of the Vertebrate Secretome
BACKGROUND: Understanding the functional role(s) of the more than 20,000 proteins of the vertebrate genome is a major next step in the post-genome era. The approximately 4,000 co-translationally translocated (CTT) proteins – representing the vertebrate secretome – are important for such vertebrate-c...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1766371/ https://www.ncbi.nlm.nih.gov/pubmed/17218990 http://dx.doi.org/10.1371/journal.pone.0000104 |
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author | Pickart, Michael A. Klee, Eric W. Nielsen, Aubrey L. Sivasubbu, Sridhar Mendenhall, Eric M. Bill, Brent R. Chen, Eleanor Eckfeldt, Craig E. Knowlton, Michelle Robu, Mara E. Larson, Jon D. Deng, Yun Schimmenti, Lisa A. Ellis, Lynda B.M. Verfaillie, Catherine M. Hammerschmidt, Matthias Farber, Steven A. Ekker, Stephen C. |
author_facet | Pickart, Michael A. Klee, Eric W. Nielsen, Aubrey L. Sivasubbu, Sridhar Mendenhall, Eric M. Bill, Brent R. Chen, Eleanor Eckfeldt, Craig E. Knowlton, Michelle Robu, Mara E. Larson, Jon D. Deng, Yun Schimmenti, Lisa A. Ellis, Lynda B.M. Verfaillie, Catherine M. Hammerschmidt, Matthias Farber, Steven A. Ekker, Stephen C. |
author_sort | Pickart, Michael A. |
collection | PubMed |
description | BACKGROUND: Understanding the functional role(s) of the more than 20,000 proteins of the vertebrate genome is a major next step in the post-genome era. The approximately 4,000 co-translationally translocated (CTT) proteins – representing the vertebrate secretome – are important for such vertebrate-critical processes as organogenesis. However, the role(s) for most of these genes is currently unknown. RESULTS: We identified 585 putative full-length zebrafish CTT proteins using cross-species genomic and EST-based comparative sequence analyses. We further investigated 150 of these genes (Figure 1) for unique function using morpholino-based analysis in zebrafish embryos. 12% of the CTT protein-deficient embryos resulted in specific developmental defects, a notably higher rate of gene function annotation than the 2%–3% estimate from random gene mutagenesis studies. CONCLUSION(S): This initial collection includes novel genes required for the development of vascular, hematopoietic, pigmentation, and craniofacial tissues, as well as lipid metabolism, and organogenesis. This study provides a framework utilizing zebrafish for the systematic assignment of biological function in a vertebrate genome. |
format | Text |
id | pubmed-1766371 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-17663712007-01-11 Genome-Wide Reverse Genetics Framework to Identify Novel Functions of the Vertebrate Secretome Pickart, Michael A. Klee, Eric W. Nielsen, Aubrey L. Sivasubbu, Sridhar Mendenhall, Eric M. Bill, Brent R. Chen, Eleanor Eckfeldt, Craig E. Knowlton, Michelle Robu, Mara E. Larson, Jon D. Deng, Yun Schimmenti, Lisa A. Ellis, Lynda B.M. Verfaillie, Catherine M. Hammerschmidt, Matthias Farber, Steven A. Ekker, Stephen C. PLoS One Research Article BACKGROUND: Understanding the functional role(s) of the more than 20,000 proteins of the vertebrate genome is a major next step in the post-genome era. The approximately 4,000 co-translationally translocated (CTT) proteins – representing the vertebrate secretome – are important for such vertebrate-critical processes as organogenesis. However, the role(s) for most of these genes is currently unknown. RESULTS: We identified 585 putative full-length zebrafish CTT proteins using cross-species genomic and EST-based comparative sequence analyses. We further investigated 150 of these genes (Figure 1) for unique function using morpholino-based analysis in zebrafish embryos. 12% of the CTT protein-deficient embryos resulted in specific developmental defects, a notably higher rate of gene function annotation than the 2%–3% estimate from random gene mutagenesis studies. CONCLUSION(S): This initial collection includes novel genes required for the development of vascular, hematopoietic, pigmentation, and craniofacial tissues, as well as lipid metabolism, and organogenesis. This study provides a framework utilizing zebrafish for the systematic assignment of biological function in a vertebrate genome. Public Library of Science 2006-12-20 /pmc/articles/PMC1766371/ /pubmed/17218990 http://dx.doi.org/10.1371/journal.pone.0000104 Text en Pickart et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Pickart, Michael A. Klee, Eric W. Nielsen, Aubrey L. Sivasubbu, Sridhar Mendenhall, Eric M. Bill, Brent R. Chen, Eleanor Eckfeldt, Craig E. Knowlton, Michelle Robu, Mara E. Larson, Jon D. Deng, Yun Schimmenti, Lisa A. Ellis, Lynda B.M. Verfaillie, Catherine M. Hammerschmidt, Matthias Farber, Steven A. Ekker, Stephen C. Genome-Wide Reverse Genetics Framework to Identify Novel Functions of the Vertebrate Secretome |
title | Genome-Wide Reverse Genetics Framework to Identify Novel Functions of the Vertebrate Secretome |
title_full | Genome-Wide Reverse Genetics Framework to Identify Novel Functions of the Vertebrate Secretome |
title_fullStr | Genome-Wide Reverse Genetics Framework to Identify Novel Functions of the Vertebrate Secretome |
title_full_unstemmed | Genome-Wide Reverse Genetics Framework to Identify Novel Functions of the Vertebrate Secretome |
title_short | Genome-Wide Reverse Genetics Framework to Identify Novel Functions of the Vertebrate Secretome |
title_sort | genome-wide reverse genetics framework to identify novel functions of the vertebrate secretome |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1766371/ https://www.ncbi.nlm.nih.gov/pubmed/17218990 http://dx.doi.org/10.1371/journal.pone.0000104 |
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