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Expansion of tandem repeats in sea anemone Nematostella vectensis proteome: A source for gene novelty?

BACKGROUND: The complete proteome of the starlet sea anemone, Nematostella vectensis, provides insights into gene invention dating back to the Cnidarian-Bilaterian ancestor. With the addition of the complete proteomes of Hydra magnipapillata and Monosiga brevicollis, the investigation of proteins ha...

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Autores principales: Naamati, Guy, Fromer, Menachem, Linial, Michal
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2805694/
https://www.ncbi.nlm.nih.gov/pubmed/20003297
http://dx.doi.org/10.1186/1471-2164-10-593
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author Naamati, Guy
Fromer, Menachem
Linial, Michal
author_facet Naamati, Guy
Fromer, Menachem
Linial, Michal
author_sort Naamati, Guy
collection PubMed
description BACKGROUND: The complete proteome of the starlet sea anemone, Nematostella vectensis, provides insights into gene invention dating back to the Cnidarian-Bilaterian ancestor. With the addition of the complete proteomes of Hydra magnipapillata and Monosiga brevicollis, the investigation of proteins having unique features in early metazoan life has become practical. We focused on the properties and the evolutionary trends of tandem repeat (TR) sequences in Cnidaria proteomes. RESULTS: We found that 11-16% of N. vectensis proteins contain tandem repeats. Most TRs cover 150 amino acid segments that are comprised of basic units of 5-20 amino acids. In total, the N. Vectensis proteome has about 3300 unique TR-units, but only a small fraction of them are shared with H. magnipapillata, M. brevicollis, or mammalian proteomes. The overall abundance of these TRs stands out relative to that of 14 proteomes representing the diversity among eukaryotes and within the metazoan world. TR-units are characterized by a unique composition of amino acids, with cysteine and histidine being over-represented. Structurally, most TR-segments are associated with coiled and disordered regions. Interestingly, 80% of the TR-segments can be read in more than one open reading frame. For over 100 of them, translation of the alternative frames would result in long proteins. Most domain families that are characterized as repeats in eukaryotes are found in the TR-proteomes from Nematostella and Hydra. CONCLUSIONS: While most TR-proteins have originated from prediction tools and are still awaiting experimental validations, supportive evidence exists for hundreds of TR-units in Nematostella. The existence of TR-proteins in early metazoan life may have served as a robust mode for novel genes with previously overlooked structural and functional characteristics.
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spelling pubmed-28056942010-01-13 Expansion of tandem repeats in sea anemone Nematostella vectensis proteome: A source for gene novelty? Naamati, Guy Fromer, Menachem Linial, Michal BMC Genomics Research article BACKGROUND: The complete proteome of the starlet sea anemone, Nematostella vectensis, provides insights into gene invention dating back to the Cnidarian-Bilaterian ancestor. With the addition of the complete proteomes of Hydra magnipapillata and Monosiga brevicollis, the investigation of proteins having unique features in early metazoan life has become practical. We focused on the properties and the evolutionary trends of tandem repeat (TR) sequences in Cnidaria proteomes. RESULTS: We found that 11-16% of N. vectensis proteins contain tandem repeats. Most TRs cover 150 amino acid segments that are comprised of basic units of 5-20 amino acids. In total, the N. Vectensis proteome has about 3300 unique TR-units, but only a small fraction of them are shared with H. magnipapillata, M. brevicollis, or mammalian proteomes. The overall abundance of these TRs stands out relative to that of 14 proteomes representing the diversity among eukaryotes and within the metazoan world. TR-units are characterized by a unique composition of amino acids, with cysteine and histidine being over-represented. Structurally, most TR-segments are associated with coiled and disordered regions. Interestingly, 80% of the TR-segments can be read in more than one open reading frame. For over 100 of them, translation of the alternative frames would result in long proteins. Most domain families that are characterized as repeats in eukaryotes are found in the TR-proteomes from Nematostella and Hydra. CONCLUSIONS: While most TR-proteins have originated from prediction tools and are still awaiting experimental validations, supportive evidence exists for hundreds of TR-units in Nematostella. The existence of TR-proteins in early metazoan life may have served as a robust mode for novel genes with previously overlooked structural and functional characteristics. BioMed Central 2009-12-10 /pmc/articles/PMC2805694/ /pubmed/20003297 http://dx.doi.org/10.1186/1471-2164-10-593 Text en Copyright ©2009 Naamati et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research article
Naamati, Guy
Fromer, Menachem
Linial, Michal
Expansion of tandem repeats in sea anemone Nematostella vectensis proteome: A source for gene novelty?
title Expansion of tandem repeats in sea anemone Nematostella vectensis proteome: A source for gene novelty?
title_full Expansion of tandem repeats in sea anemone Nematostella vectensis proteome: A source for gene novelty?
title_fullStr Expansion of tandem repeats in sea anemone Nematostella vectensis proteome: A source for gene novelty?
title_full_unstemmed Expansion of tandem repeats in sea anemone Nematostella vectensis proteome: A source for gene novelty?
title_short Expansion of tandem repeats in sea anemone Nematostella vectensis proteome: A source for gene novelty?
title_sort expansion of tandem repeats in sea anemone nematostella vectensis proteome: a source for gene novelty?
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2805694/
https://www.ncbi.nlm.nih.gov/pubmed/20003297
http://dx.doi.org/10.1186/1471-2164-10-593
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