Biology:CRYM
 Generic protein structure example |
Mu-crystallin homolog also known as NADP-regulated thyroid-hormone-binding protein (THBP) is a protein that in humans is encoded by the CRYM gene. Multiple alternatively spliced transcript variants have been found for this gene.[1][2]
Function
Crystallins are separated into two classes: taxon-specific and ubiquitous. The former class is also called phylogenetically-restricted crystallins. The latter class constitutes the major proteins of vertebrate eye lens and maintains the transparency and refractive index of the lens. This gene encodes a taxon-specific crystallin protein that binds NADPH and has sequence similarity to bacterial ornithine cyclodeaminases. The encoded protein does not perform a structural role in lens tissue, and instead it binds thyroid hormone for possible regulatory or developmental roles.[2]
Its enzyme function has been determined as a ketimine reductase, reducing cyclic ketimines to their reduced forms. Either NADH or NADPH can be used as cofactor. The most active substrate at pH 5.0 is aminoethylcysteine ketimine (AECK), however at neutral pH (pH 7.2) the most active substrate is 1-piperideine-2-carboxylate which is an important part of the pipecolic acid pathway. The active form of thyroxine, T3, has been found to be a potent inhibitor at nanomolar concentrations.[3]
Besides its role in lens biology, CRYM seems also to be involved in thyroid hormone signalling in other tissues. It could be demonstrated that CRYM mutations may cause deafness through thyroid hormone binding effects on the fibrocytes of the cochlea.[4] Disruption of the CRYM gene leads to decreased T3 concentrations in both tissues and serum without alteration of peripheral T3 action in vivo.[5][6]
The existence of intracellular thyroid hormone binding proteins has been postulated from mathematical modelling of pituitary-thyroid homeostasis.[7] Binding properties have been assumed to be similar to those of extracellular binding proteins,[8] however it is not clear, if THBP is the only intracellular thyroid hormone binding protein.
References
- ↑ "Localization of the human gene for mu-crystallin to chromosome 16p". Genomics 14 (4): 1115–6. Feb 1993. doi:10.1016/S0888-7543(05)80143-0. PMID 1478656.
- ↑ 2.0 2.1 "Entrez Gene: CRYM crystallin, mu". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=1428.
- ↑ "Mammalian forebrain ketimine reductase identified as μ-crystallin; potential regulation by thyroid hormones". J Neurochem 118 (3): 379–387. February 2011. doi:10.1111/j.1471-4159.2011.07220.x. PMID 21332720.
- ↑ "CRYM mutations cause deafness through thyroid hormone binding properties in the fibrocytes of the cochlea". J. Med. Genet. 43 (6): e25. June 2006. doi:10.1136/jmg.2005.034397. PMID 16740909.
- ↑ "Identification of CRYM as a candidate responsible for nonsyndromic deafness, through cDNA microarray analysis of human cochlear and vestibular tissues". Am. J. Hum. Genet. 72 (1): 73–82. January 2003. doi:10.1086/345398. PMID 12471561.
- ↑ "micro-Crystallin as an intracellular 3,5,3'-triiodothyronine holder in vivo". Mol. Endocrinol. 21 (4): 885–94. April 2007. doi:10.1210/me.2006-0403. PMID 17264173.
- ↑ Dietrich JW (2002) (in de). Der Hypophysen-Schilddrüsen-Regelkreis. Entwicklung und klinische Anwendung eines nichtlinearen Modells.. Berlin: Logos-Verlag. ISBN 3-89722-850-5.
- ↑ "Thyrotropic Feedback Control: Evidence for an Additional Ultrashort Feedback Loop from Fractal Analysis". Cybernetics and Systems 35 (4): 315–31. 2004. doi:10.1080/01969720490443354.
External links
- Human CRYM genome location and CRYM gene details page in the UCSC Genome Browser.
Further reading
- "mu-crystallin is a mammalian homologue of Agrobacterium ornithine cyclodeaminase and is expressed in human retina". Proc. Natl. Acad. Sci. U.S.A. 89 (19): 9292–6. 1992. doi:10.1073/pnas.89.19.9292. PMID 1384048. Bibcode: 1992PNAS...89.9292K.
- "High affinity thyroid hormone-binding protein in human kidney: kinetic characterization and identification by photoaffinity labeling". Endocrinology 137 (11): 4563–70. 1996. doi:10.1210/en.137.11.4563. PMID 8895318.
- "Two roles for mu-crystallin: a lens structural protein in diurnal marsupials and a possible enzyme in mammalian retinas". Mol. Vis. 3: 9. 1998. PMID 9285773.
- "Purification, molecular cloning, and functional expression of the human nicodinamide-adenine dinucleotide phosphate-regulated thyroid hormone-binding protein". Mol. Endocrinol. 11 (11): 1728–36. 1998. doi:10.1210/mend.11.11.9915. PMID 9328354.
- "Genome duplications and other features in 12 Mb of DNA sequence from human chromosome 16p and 16q". Genomics 60 (3): 295–308. 1999. doi:10.1006/geno.1999.5927. PMID 10493829.
- "Identification of CRYM as a candidate responsible for nonsyndromic deafness, through cDNA microarray analysis of human cochlear and vestibular tissues". Am. J. Hum. Genet. 72 (1): 73–82. 2003. doi:10.1086/345398. PMID 12471561.
- "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. 2003. doi:10.1073/pnas.242603899. PMID 12477932. Bibcode: 2002PNAS...9916899M.
- "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. 2004. doi:10.1101/gr.2596504. PMID 15489334.
- "Abnormal expression of mu-crystallin in facioscapulohumeral muscular dystrophy". Exp. Neurol. 205 (2): 583–6. 2007. doi:10.1016/j.expneurol.2007.03.009. PMID 17451686.
PDB gallery | |
|---|---|
|
 |  |
