Cartilage associated protein

CRTAP
Identifiers
Aliases	CRTAP, CASP, LEPREL3, OI7, P3H5, cartilage associated protein
External IDs	OMIM: 605497; MGI: 1891221; HomoloGene: 21280; GeneCards: CRTAP; OMA:CRTAP - orthologs
Gene location (Human)
Chr.	Chromosome 3 (human)
End	33,147,773 bp
Gene location (Mouse)
Chr.	Chromosome 9 (mouse)
End	114,219,743 bp
RNA expression pattern
	Top expressed in
	tendon of biceps brachii; ; stromal cell of endometrium; ; canal of the cervix; ; Descending thoracic aorta; ; right coronary artery; ; ascending aorta; ; body of uterus; ; gallbladder; ; popliteal artery; ; tibial arteries;
	Top expressed in
	calvaria; ; body of femur; ; molar; ; stroma of bone marrow; ; efferent ductule; ; dermis; ; external carotid artery; ; sciatic nerve; ; atrium; ; internal carotid artery;
	More reference expression data
	n/a
Gene ontology
Molecular function	protein-containing complex binding; protein binding;
Cellular component	extracellular region; protein-containing complex; endoplasmic reticulum lumen; endoplasmic reticulum; extracellular space;
Biological process	protein stabilization; negative regulation of post-translational protein modification; spermatogenesis; peptidyl-proline hydroxylation to 3-hydroxy-L-proline; chaperone-mediated protein folding;
	Sources:Amigo / QuickGO
Orthologs
	10491
	56693
	ENSG00000170275
	ENSMUSG00000032431
	O75718
	Q9CYD3
	NM_006371
	NM_019922
	NP_006362
	NP_064306
	Wikidata
View/Edit Human	View/Edit Mouse

Cartilage associated protein is a protein that in humans is encoded by the CRTAP gene.^[5]^[6]

Structure and function

The protein encoded by this gene is similar to the chicken and mouse CRTAP genes. The encoded protein is a scaffolding protein that may influence the activity of at least one member of the cytohesin/ARNO family in response to specific cellular stimuli.^[5]

CRTAP forms a tight protein complex with two other enzymes involved in post-translational modification: Leprecan (P3H1) and PPIB.^[7] In this complex, CRTAP acts as a collagen-binding site, capturing substrates for subsequent enzymatic processing by P3H1 and PPIB. Notably, CRTAP exhibits a folding pattern similar to the N-terminal domain of P3H1.

Clinical significance

Mutations in the CRTAP gene are associated with osteogenesis imperfecta, types VII and IIB, a connective tissue disorder characterized by bone fragility and low bone mass.^[8]^[9]

References

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000170275 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000032431 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ ^a ^b "Entrez Gene: cartilage associated protein".
^ Tonachini L, Morello R, Monticone M, Skaug J, Scherer SW, Cancedda R, et al. (1999). "cDNA cloning, characterization and chromosome mapping of the gene encoding human cartilage associated protein (CRTAP)". Cytogenetics and Cell Genetics. 87 (3–4): 191–194. doi:10.1159/000015463. PMID 10702664. S2CID 24887051.
^ Li W, Peng J, Yao D, Rao B, Xia Y, Wang Q, et al. (September 2024). "The structural basis for the collagen processing by human P3H1/CRTAP/PPIB ternary complex". Nature Communications. 15 (1): 7844. doi:10.1038/s41467-024-52321-6. PMC 11381544. PMID 39245686.
^ Barnes AM, Chang W, Morello R, Cabral WA, Weis M, Eyre DR, et al. (December 2006). "Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta". The New England Journal of Medicine. 355 (26): 2757–2764. doi:10.1056/NEJMoa063804. PMC 7509984. PMID 17192541.
^ Baldridge D, Schwarze U, Morello R, Lennington J, Bertin TK, Pace JM, et al. (December 2008). "CRTAP and LEPRE1 mutations in recessive osteogenesis imperfecta". Human Mutation. 29 (12): 1435–1442. doi:10.1002/humu.20799. PMC 2671575. PMID 18566967.

Marini JC, Cabral WA, Barnes AM (January 2010). "Null mutations in LEPRE1 and CRTAP cause severe recessive osteogenesis imperfecta". Cell and Tissue Research. 339 (1): 59–70. doi:10.1007/s00441-009-0872-0. PMC 3156555. PMID 19862557.
Morello R, Bertin TK, Chen Y, Hicks J, Tonachini L, Monticone M, et al. (October 2006). "CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta". Cell. 127 (2): 291–304. doi:10.1016/j.cell.2006.08.039. PMID 17055431. S2CID 8123837.
Chang W, Barnes AM, Cabral WA, Bodurtha JN, Marini JC (January 2010). "Prolyl 3-hydroxylase 1 and CRTAP are mutually stabilizing in the endoplasmic reticulum collagen prolyl 3-hydroxylation complex". Human Molecular Genetics. 19 (2): 223–234. doi:10.1093/hmg/ddp481. PMC 2796888. PMID 19846465.
Li GH, Kung AW, Huang QY (June 2010). "Common variants in FLNB/CRTAP, not ARHGEF3 at 3p, are associated with osteoporosis in southern Chinese women". Osteoporosis International. 21 (6): 1009–1020. doi:10.1007/s00198-009-1043-6. PMC 2946578. PMID 19727905.
Bodian DL, Chan TF, Poon A, Schwarze U, Yang K, Byers PH, et al. (February 2009). "Mutation and polymorphism spectrum in osteogenesis imperfecta type II: implications for genotype-phenotype relationships". Human Molecular Genetics. 18 (3): 463–471. doi:10.1093/hmg/ddn374. PMC 2638801. PMID 18996919.
Morello R, Tonachini L, Monticone M, Viggiano L, Rocchi M, Cancedda R, et al. (June 1999). "cDNA cloning, characterization and chromosome mapping of Crtap encoding the mouse cartilage associated protein". Matrix Biology. 18 (3): 319–324. doi:10.1016/S0945-053X(99)00002-5. PMID 10429950.
Kimura K, Wakamatsu A, Suzuki Y, Ota T, Nishikawa T, Yamashita R, et al. (January 2006). "Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes". Genome Research. 16 (1): 55–65. doi:10.1101/gr.4039406. PMC 1356129. PMID 16344560.
Castagnola P, Gennari M, Morello R, Tonachini L, Marin O, Gaggero A, et al. (June 1997). "Cartilage associated protein (CASP) is a novel developmentally regulated chick embryo protein". Journal of Cell Science. 110. 110 (12): 1351–1359. doi:10.1242/jcs.110.12.1351. PMID 9217321.
Sowa ME, Bennett EJ, Gygi SP, Harper JW (July 2009). "Defining the human deubiquitinating enzyme interaction landscape". Cell. 138 (2): 389–403. doi:10.1016/j.cell.2009.04.042. PMC 2716422. PMID 19615732.
Van Dijk FS, Nesbitt IM, Nikkels PG, Dalton A, Bongers EM, van de Kamp JM, et al. (December 2009). "CRTAP mutations in lethal and severe osteogenesis imperfecta: the importance of combining biochemical and molecular genetic analysis". European Journal of Human Genetics. 17 (12): 1560–1569. doi:10.1038/ejhg.2009.75. PMC 2987020. PMID 19550437.

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

This article on a gene on human chromosome 3 is a stub. You can help Wikipedia by expanding it.

[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000170275 – Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000032431 – Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[entrez-5] "Entrez Gene: cartilage associated protein".

[pmid10702664-6] Tonachini L, Morello R, Monticone M, Skaug J, Scherer SW, Cancedda R, et al. (1999). "cDNA cloning, characterization and chromosome mapping of the gene encoding human cartilage associated protein (CRTAP)". Cytogenetics and Cell Genetics. 87 (3–4): 191–194. doi:10.1159/000015463. PMID 10702664. S2CID 24887051.

[7] Li W, Peng J, Yao D, Rao B, Xia Y, Wang Q, et al. (September 2024). "The structural basis for the collagen processing by human P3H1/CRTAP/PPIB ternary complex". Nature Communications. 15 (1): 7844. doi:10.1038/s41467-024-52321-6. PMC 11381544. PMID 39245686.

[pmid17192541-8] Barnes AM, Chang W, Morello R, Cabral WA, Weis M, Eyre DR, et al. (December 2006). "Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta". The New England Journal of Medicine. 355 (26): 2757–2764. doi:10.1056/NEJMoa063804. PMC 7509984. PMID 17192541.

[pmid18566967-9] Baldridge D, Schwarze U, Morello R, Lennington J, Bertin TK, Pace JM, et al. (December 2008). "CRTAP and LEPRE1 mutations in recessive osteogenesis imperfecta". Human Mutation. 29 (12): 1435–1442. doi:10.1002/humu.20799. PMC 2671575. PMID 18566967.

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Structure and function

Clinical significance

References

Further reading