A revised nomenclature for transcribed human endogenous retroviral loci
<p>Abstract</p> <p>Background</p> <p>Endogenous retroviruses (ERVs) and ERV-like sequences comprise 8% of the human genome. A hitherto unknown proportion of ERV loci are transcribed and thus contribute to the human transcriptome. A small proportion of these loci encode...
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doaj-3e405057cc144d81a39005d5f16279f42020-11-25T00:14:37ZengBMCMobile DNA1759-87532011-05-0121710.1186/1759-8753-2-7A revised nomenclature for transcribed human endogenous retroviral lociMayer JensBlomberg JonasSeal Ruth L<p>Abstract</p> <p>Background</p> <p>Endogenous retroviruses (ERVs) and ERV-like sequences comprise 8% of the human genome. A hitherto unknown proportion of ERV loci are transcribed and thus contribute to the human transcriptome. A small proportion of these loci encode functional proteins. As the role of ERVs in normal and diseased biological processes is not yet established, transcribed ERV loci are of particular interest. As more transcribed ERV loci are likely to be identified in the near future, the development of a systematic nomenclature is important to ensure that all information on each locus can be easily retrieved.</p> <p>Results</p> <p>Here we present a revised nomenclature of transcribed human endogenous retroviral loci that sorts loci into groups based on Repbase classifications. Each symbol is of the format ERV + group symbol + unique number. Group symbols are based on a mixture of Repbase designations and well-supported symbols used in the literature. The presented guidelines will allow newly identified loci to be easily incorporated into the scheme.</p> <p>Conclusions</p> <p>The naming system will be employed by the HUGO Gene Nomenclature Committee for naming transcribed human ERV loci. We hope that the system will contribute to clarifying a certain aspect of a sometimes confusing nomenclature for human endogenous retroviruses. The presented system may also be employed for naming transcribed loci of human non-ERV repeat loci.</p> http://www.mobilednajournal.com/content/2/1/7 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Mayer Jens Blomberg Jonas Seal Ruth L |
spellingShingle |
Mayer Jens Blomberg Jonas Seal Ruth L A revised nomenclature for transcribed human endogenous retroviral loci Mobile DNA |
author_facet |
Mayer Jens Blomberg Jonas Seal Ruth L |
author_sort |
Mayer Jens |
title |
A revised nomenclature for transcribed human endogenous retroviral loci |
title_short |
A revised nomenclature for transcribed human endogenous retroviral loci |
title_full |
A revised nomenclature for transcribed human endogenous retroviral loci |
title_fullStr |
A revised nomenclature for transcribed human endogenous retroviral loci |
title_full_unstemmed |
A revised nomenclature for transcribed human endogenous retroviral loci |
title_sort |
revised nomenclature for transcribed human endogenous retroviral loci |
publisher |
BMC |
series |
Mobile DNA |
issn |
1759-8753 |
publishDate |
2011-05-01 |
description |
<p>Abstract</p> <p>Background</p> <p>Endogenous retroviruses (ERVs) and ERV-like sequences comprise 8% of the human genome. A hitherto unknown proportion of ERV loci are transcribed and thus contribute to the human transcriptome. A small proportion of these loci encode functional proteins. As the role of ERVs in normal and diseased biological processes is not yet established, transcribed ERV loci are of particular interest. As more transcribed ERV loci are likely to be identified in the near future, the development of a systematic nomenclature is important to ensure that all information on each locus can be easily retrieved.</p> <p>Results</p> <p>Here we present a revised nomenclature of transcribed human endogenous retroviral loci that sorts loci into groups based on Repbase classifications. Each symbol is of the format ERV + group symbol + unique number. Group symbols are based on a mixture of Repbase designations and well-supported symbols used in the literature. The presented guidelines will allow newly identified loci to be easily incorporated into the scheme.</p> <p>Conclusions</p> <p>The naming system will be employed by the HUGO Gene Nomenclature Committee for naming transcribed human ERV loci. We hope that the system will contribute to clarifying a certain aspect of a sometimes confusing nomenclature for human endogenous retroviruses. The presented system may also be employed for naming transcribed loci of human non-ERV repeat loci.</p> |
url |
http://www.mobilednajournal.com/content/2/1/7 |
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