TSHB
| Tireostimulišući hormon, beta | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Identifikatori | |||||||||||
| Simboli | TSHB; TSH-B; TSH-BETA | ||||||||||
| Vanjski ID | OMIM: 188540 MGI: 98848 HomoloGene: 463 GeneCards: TSHB Gene | ||||||||||
| |||||||||||
| Ortolozi | |||||||||||
| Vrsta | Čovek | Miš | |||||||||
| Entrez | 7252 | 22094 | |||||||||
| Ensembl | ENSG00000134200 | ENSMUSG00000027857 | |||||||||
| UniProt | P01222 | E9Q4F3 | |||||||||
| RefSeq (mRNA) | NM_000549.3 | NM_001165939.1 | |||||||||
| RefSeq (protein) | NP_000540.2 | NP_001159411.1 | |||||||||
| Lokacija (UCSC) |
Chr 1: 115.57 - 115.58 Mb |
Chr 3: 102.78 - 102.78 Mb | |||||||||
| PubMed pretraga | [1] | [2] | |||||||||
Tireostimulišući hormon, beta (TSHB) je protein koji je kod ljudi kodiran TSHB genom.[1][2]
Funkcija
Tireostimulišući hormon (TSH) je nekovalentno vezani glikoproteinski heterodimer. On je deo familije hipofiznih hormona koji sadrže zajedničku alfa podjedinicu (TSHA) i jedinstvenu beta podjedinicu (ovaj protein) koja daje specifičnost.[3]
Reference
- ^ Wondisford FE, Radovick S, Moates JM, Usala SJ, Weintraub BD (1988). „Isolation and characterization of the human thyrotropin beta-subunit gene. Differences in gene structure and promoter function from murine species”. J. Biol. Chem.. 263 (25): 12538—42. PMID 2457586. Архивирано из оригинала 25. 04. 2020. г. Приступљено 26. 12. 2012.
- ^ Tatsumi K, Hayashizaki Y, Hiraoka Y, Miyai K, Matsubara K (1988). „The structure of the human thyrotropin beta-subunit gene”. Gene. 73 (2): 489—97. PMID 3243440. doi:10.1016/0378-1119(88)90513-6.
- ^ „Entrez Gene: TSHB”.
Literatura
- Bonomi M; Proverbio MC; Weber G; et al. (2001). „Hyperplastic pituitary gland, high serum glycoprotein hormone alpha-subunit, and variable circulating thyrotropin (TSH) levels as hallmark of central hypothyroidism due to mutations of the TSH beta gene.”. J. Clin. Endocrinol. Metab.. 86 (4): 1600—4. PMID 11297590. doi:10.1210/jc.86.4.1600.
- Vuissoz JM; Deladoëy J; Buyukgebiz A; et al. (2001). „New autosomal recessive mutation of the TSH-beta subunit gene causing central isolated hypothyroidism.”. J. Clin. Endocrinol. Metab.. 86 (9): 4468—71. PMID 11549695. doi:10.1210/jc.86.9.4468.
- Karges B; LeHeup B; Schoenle E; et al. (2004). „Compound heterozygous and homozygous mutations of the TSHbeta gene as a cause of congenital central hypothyroidism in Europe.”. Horm. Res.. 62 (3): 149—55. PMID 15297803. doi:10.1159/000080071.
- Kabadi UM, Premachandra BN (2007). „Serum thyrotropin in Graves' disease: a more reliable index of circulating thyroid-stimulating immunoglobulin level than thyroid function?”. Endocr Pract. 13 (6): 615—9. PMID 17954417.
- Miyai S; Yoshimura S; Iwasaki Y; et al. (2005). „Induction of GH, PRL, and TSH beta mRNA by transfection of Pit-1 in a human pituitary adenoma-derived cell line.”. Cell Tissue Res.. 322 (2): 269—77. PMID 16133148. doi:10.1007/s00441-005-0033-z.
- Pierce JG (1971). „Eli Lilly lecture. The subunits of pituitary thyrotropin--their relationship to other glycoprotein hormones.”. Endocrinology. 89 (6): 1331—44. PMID 5002675. doi:10.1210/endo-89-6-1331.
- Atzmon G, Barzilai N, Surks MI, Gabriely I (2009). „Genetic Predisposition to Elevated Serum Thyrotropin Is Associated with Exceptional Longevity”. J. Clin. Endocrinol. Metab.. 94 (12): 4768—75. PMC 2795660
. PMID 19837933. doi:10.1210/jc.2009-0808. - Landa I, Ruiz-Llorente S, Montero-Conde C; et al. (2009). Gibson, Greg, ур. „The Variant rs1867277 in FOXE1 Gene Confers Thyroid Cancer Susceptibility through the Recruitment of USF1/USF2 Transcription Factors”. PLoS Genet.. 5 (9): e1000637. PMC 2727793 . PMID 19730683. doi:10.1371/journal.pgen.1000637.
- Pohlenz J; Dumitrescu A; Aumann U; et al. (2002). „Congenital secondary hypothyroidism caused by exon skipping due to a homozygous donor splice site mutation in the TSHbeta-subunit gene”. J. Clin. Endocrinol. Metab.. 87 (1): 336—9. PMID 11788671. doi:10.1210/jc.87.1.336.
- Miyoshi I, Kasai N, Hayashizaki Y (1994). „[Structure and regulation of human thyroid-stimulating hormone (TSH) gene]”. Nippon Rinsho. 52 (4): 940—7. PMID 8196184.
- Borck G; Topaloglu AK; Korsch E; et al. (2004). „Four new cases of congenital secondary hypothyroidism due to a splice site mutation in the thyrotropin-beta gene: phenotypic variability and founder effect”. J. Clin. Endocrinol. Metab.. 89 (8): 4136—41. PMID 15292359. doi:10.1210/jc.2004-0494.
- Comings DE; Gade-Andavolu R; Gonzalez N; et al. (2000). „A multivariate analysis of 59 candidate genes in personality traits: the temperament and character inventory”. Clin. Genet.. 58 (5): 375—85. PMID 11140838. doi:10.1034/j.1399-0004.2000.580508.x.
- Gerhard DS; Wagner L; Feingold EA; et al. (2004). „The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)”. Genome Res.. 14 (10B): 2121—7. PMC 528928 . PMID 15489334. doi:10.1101/gr.2596504.
- Clark AG; Glanowski S; Nielsen R; et al. (2003). „Inferring nonneutral evolution from human-chimp-mouse orthologous gene trios”. Science. 302 (5652): 1960—3. PMID 14671302. doi:10.1126/science.1088821.
- Loinder K, Söderström M (2005). „An LXXLL motif in nuclear receptor corepressor mediates ligand-induced repression of the thyroid stimulating hormone-beta gene”. J. Steroid Biochem. Mol. Biol.. 97 (4): 322—7. PMID 16216492. doi:10.1016/j.jsbmb.2005.06.031.
- Luttrell LM (2008). „Reviews in molecular biology and biotechnology: transmembrane signaling by G protein-coupled receptors”. Mol. Biotechnol.. 39 (3): 239—64. PMID 18240029. doi:10.1007/s12033-008-9031-1.
- Strausberg RL; Feingold EA; Grouse LH; et al. (2002). „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. PMC 139241 . PMID 12477932. doi:10.1073/pnas.242603899.
- Brumm H; Pfeufer A; Biebermann H; et al. (2002). „Congenital central hypothyroidism due to homozygous thyrotropin beta 313 Delta T mutation is caused by a Founder effect”. J. Clin. Endocrinol. Metab.. 87 (10): 4811—6. PMID 12364478. doi:10.1210/jc.2002-020297.
- Benhadi N; Wiersinga WM; Reitsma JB; et al. (2009). „Higher maternal TSH levels in pregnancy are associated with increased risk for miscarriage, fetal or neonatal death”. Eur. J. Endocrinol.. 160 (6): 985—91. PMID 19273570. doi:10.1530/EJE-08-0953.
- Schaefer JS, Klein JR (2009). „A novel thyroid stimulating hormone β-subunit isoform in human pituitary, peripheral blood leukocytes, and thyroid”. Gen. Comp. Endocrinol.. 162 (3): 241—4. PMC 2689139 . PMID 19364510. doi:10.1016/j.ygcen.2009.04.006.
Vidi još
Content Disclaimer
Informasi ini disarikan dari Wikipedia dan disajikan kembali untuk tujuan edukasi. Konten tersedia di bawah lisensi CC BY-SA 3.0. Kami tidak bertanggung jawab atas ketidakakuratan data yang bersumber dari kontribusi publik tersebut.
- The information displayed on this website is sourced in part or in whole from Wikipedia and has been adapted for the purpose of restating it. We strive to provide accurate and relevant information, however:
- There is no guarantee of absolute accuracy. Wikipedia is an open, collaborative project that can be edited by anyone, so information is subject to change.
- It is not intended to constitute professional advice. The content displayed is for informational and educational purposes only. For important decisions (e.g., medical, legal, or financial), please consult a professional.
- Content copyright. Wikipedia is licensed under the Creative Commons Attribution-ShareAlike License (CC BY-SA). This means that content may be reused with appropriate attribution and shared under a similar license.
- Responsible use. Any risk arising from the use of information from this website is entirely the responsibility of the user.