Cargando…
The human crystallin gene families
Crystallins are the abundant, long-lived proteins of the eye lens. The major human crystallins belong to two different superfamilies: the small heat-shock proteins (α-crystallins) and the βγ-crystallins. During evolution, other proteins have sometimes been recruited as crystallins to modify the prop...
Autor principal: | |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3554465/ https://www.ncbi.nlm.nih.gov/pubmed/23199295 http://dx.doi.org/10.1186/1479-7364-6-26 |
_version_ | 1782256897078853632 |
---|---|
author | Wistow, Graeme |
author_facet | Wistow, Graeme |
author_sort | Wistow, Graeme |
collection | PubMed |
description | Crystallins are the abundant, long-lived proteins of the eye lens. The major human crystallins belong to two different superfamilies: the small heat-shock proteins (α-crystallins) and the βγ-crystallins. During evolution, other proteins have sometimes been recruited as crystallins to modify the properties of the lens. In the developing human lens, the enzyme betaine-homocysteine methyltransferase serves such a role. Evolutionary modification has also resulted in loss of expression of some human crystallin genes or of specific splice forms. Crystallin organization is essential for lens transparency and mutations; even minor changes to surface residues can cause cataract and loss of vision. |
format | Online Article Text |
id | pubmed-3554465 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35544652013-01-29 The human crystallin gene families Wistow, Graeme Hum Genomics Gene Family Update Crystallins are the abundant, long-lived proteins of the eye lens. The major human crystallins belong to two different superfamilies: the small heat-shock proteins (α-crystallins) and the βγ-crystallins. During evolution, other proteins have sometimes been recruited as crystallins to modify the properties of the lens. In the developing human lens, the enzyme betaine-homocysteine methyltransferase serves such a role. Evolutionary modification has also resulted in loss of expression of some human crystallin genes or of specific splice forms. Crystallin organization is essential for lens transparency and mutations; even minor changes to surface residues can cause cataract and loss of vision. BioMed Central 2012-12-01 /pmc/articles/PMC3554465/ /pubmed/23199295 http://dx.doi.org/10.1186/1479-7364-6-26 Text en Copyright ©2012 Wistow; 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 | Gene Family Update Wistow, Graeme The human crystallin gene families |
title | The human crystallin gene families |
title_full | The human crystallin gene families |
title_fullStr | The human crystallin gene families |
title_full_unstemmed | The human crystallin gene families |
title_short | The human crystallin gene families |
title_sort | human crystallin gene families |
topic | Gene Family Update |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3554465/ https://www.ncbi.nlm.nih.gov/pubmed/23199295 http://dx.doi.org/10.1186/1479-7364-6-26 |
work_keys_str_mv | AT wistowgraeme thehumancrystallingenefamilies AT wistowgraeme humancrystallingenefamilies |