Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2012 Dec 1;6(1):26.
doi: 10.1186/1479-7364-6-26.

The human crystallin gene families

Affiliations
Review

The human crystallin gene families

Graeme Wistow. Hum Genomics. .

Abstract

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.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Exon/intron structure of mammalian genes for α-, β- and γ-crystallins. Exons are shown as boxes with ORF in thicker boxes. CRYB genes coding for β-crystallins vary in 5-exon structure. The exons encoding the four structural motifs of the β-crystallin and γ-crystallin proteins are indicated by 1, 2, 3, and 4. Some mammals have an alternatively spliced exon in the first intron of CRYAA, but in humans this is a pseudoexon.
Figure 2
Figure 2
Phylogenetic tree of the human sHSP gene family. Sequences were extracted from the UCSC web browser. Translated ORFs were aligned and neighbor-joining trees were constructed using MEGA4 [15].
Figure 3
Figure 3
Phylogenetic tree of the humanβγ-crystallin gene superfamily. Sequences were extracted from the UCSC web browser. Translated ORFs were aligned and neighbor-joining trees were constructed as in Figure 2. AIM1, AIML, and CRYBG3 contain internal repeats corresponding to three β-crystallin-like genes in addition to regions not related to crystallin genes. For simplicity, the third, most highly conserved crystallin repeat from each gene was used for this alignment (designated AIM1cter, etc.).
Figure 4
Figure 4
Clustering of crystallin genes. Gaps, indicated by approximate sizes, contain non-crystallin genes. Gene orientations are indicated with arrows (dotted for pseudogenes).

Similar articles

Cited by

References

    1. Wistow G, Slingsby C. Structure and evolution of crystallins. The Encyclopedia of the Eye. 2010;2:229–238.
    1. Bloemendal H, De Jong W, Jaenicke R, Lubsen NH, Slingsby C, Tardieu A. Ageing and vision: structure, stability and function of lens crystallins. Prog Biophys Mol Biol. 2004;86:407–485. doi: 10.1016/j.pbiomolbio.2003.11.012. - DOI - PubMed
    1. Harding JJ, Crabbe MJC. The lens: development, proteins, metabolism and cataract. Eye. 1984;1B:207–492.
    1. Wistow G. Lens crystallins: gene recruitment and evolutionary dynamism. Trends Biochem Sci. 1993;18:301–306. doi: 10.1016/0968-0004(93)90041-K. - DOI - PubMed
    1. Piatigorsky J. Review: a case for corneal crystallins. J Ocul Pharmacol Ther. 2000;16:173–180. doi: 10.1089/jop.2000.16.173. - DOI - PubMed

MeSH terms