BAZ1B

BAZ1B
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 1F62
Identifiers
Aliases	BAZ1B, WBSCR10, WBSCR9, WSTF, bromodomain adjacent to zinc finger domain 1B
External IDs	MGI: 1353499 HomoloGene: 22651 GeneCards: BAZ1B
Gene ontology Molecular function • transferase activity • nucleotide binding • vitamin D receptor activator activity • histone kinase activity • zinc ion binding • histone binding • chromatin binding • non-membrane spanning protein tyrosine kinase activity • metal ion binding • kinase activity • protein binding • lysine-acetylated histone binding • protein tyrosine kinase activity • ATP binding Cellular component • pericentric heterochromatin • nuclear replication fork • nucleoplasm • condensed chromosome • nucleus Biological process • positive regulation of gene expression, epigenetic • chromatin remodeling • regulation of transcription, DNA-templated • phosphorylation • heart morphogenesis • chromatin assembly or disassembly • transcription, DNA-templated • cellular response to DNA damage stimulus • positive regulation of receptor activity • histone phosphorylation • chromatin-mediated maintenance of transcription • double-strand break repair • peptidyl-tyrosine phosphorylation Sources:Amigo / QuickGO
RNA expression pattern
More reference expression data
Orthologs
Species	Human	Mouse
Entrez	9031	22385
Ensembl	ENSG00000009954	ENSMUSG00000002748
UniProt	Q9UIG0	Q9Z277
RefSeq (mRNA)	NM_023005 NM_032408	NM_011714
RefSeq (protein)	NP_115784.1	NP_035844.2
Location (UCSC)	Chr 7: 73.44 – 73.52 Mb	Chr 5: 135.19 – 135.25 Mb
PubMed search	[1]	[2]
Wikidata

View/Edit Human

View/Edit Mouse

Tyrosine-protein kinase BAZ1B is an enzyme that in humans is encoded by the BAZ1B gene.^[3][4][5]

Function

This gene encodes a member of the bromodomain protein family. The bromodomain is a structural motif characteristic of proteins involved in chromatin-dependent regulation of transcription. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23.^[5]

Animal models

Model organisms have been used in the study of BAZ1B function. A conditional knockout mouse line, called Baz1b^{tm2a(KOMP)Wtsi},^[6] was generated as part of the International Knockout Mouse Consortium program — a high-throughput mutagenesis project to generate and distribute animal models of disease to interested scientists — at the Wellcome Trust Sanger Institute.^[7][8][9]

Male and female animals underwent a standardized phenotypic screen to determine the effects of deletion.^{[9][10][11][12]}

Baz1b knockout mouse phenotype

Characteristic	Abnormal
Homozygote viability	Yes[13]
Body weight	Yes[14]
Hair follicle cycling	No
Anxiety	No
Modified SHIRPA	No
Grip strength	No
Dysmorphology	No
Indirect calorimetry	Yes[15]
Glucose tolerance test	No
Auditory brainstem response	No
DEXA	Yes[16]
Radiography	Yes[17]
Body temperature	No
Eye morphology	No
Heart weight	No
Heart histology	No
Histology	No
Clinical chemistry	No
Plasma immunoglobulins	No
Haematology	No
Peripheral blood lymphocytes	No
Micronucleus test	No
Salmonella infection	Yes[18]
Citrobacter infection	No
All tests and analysis from [10][11][12]

Six significant phenotypes were reported:^[12]

• Fewer homozygous mutant mice survived to weaning than expected.
• Mutant mice had decreased body weights compared to wildtype control mice.
• Mutant mice showed increased activity, VO2 and energy expenditure, determined by indirect calorimetry.
• Radiography found teeth abnormalities.
• Dual-energy X-ray absorptiometry (DEXA) showed mutant female mice had a decrease in bone mineral density and content.
• Male heterozygous mice had higher bacterial counts after Salmonella infection.

Interactions

BAZ1B has been shown to interact with:

• CHAF1A,^[19]
• SMARCB1,^[19]
• SMARCC1,^[19]
• SMARCC2,^[19]
• SUPT16H^[19]
• TOP2B,^[19] and
• VDR.^[19]

References

1. "Human PubMed Reference:".
2. "Mouse PubMed Reference:".
3. Peoples RJ, Cisco MJ, Kaplan P, Francke U (Feb 1999). "Identification of the WBSCR9 gene, encoding a novel transcriptional regulator, in the Williams-Beuren syndrome deletion at 7q11.23". Cytogenet Cell Genet. 82 (3–4): 238–46. doi:10.1159/000015110. PMID 9858827.
4. Lu X, Meng X, Morris CA, Keating MT (Jan 1999). "A novel human gene, WSTF, is deleted in Williams syndrome". Genomics. 54 (2): 241–9. doi:10.1006/geno.1998.5578. PMID 9828126.
5. "Entrez Gene: BAZ1B bromodomain adjacent to zinc finger domain, 1B".
6. KOMP. "Baz1b^{tm2a(KOMP)Wtsi}". www.knockoutmouse.org. External link in |publisher= (help)
7. Dolgin E (June 2011). "Mouse library set to be knockout". Nature. 474 (7351): 262–263. doi:10.1038/474262a. PMID 21677718.
8. Collins FS, Rossant J, Wurst W (January 2007). "A mouse for all reasons". Cell. 128 (1): 9–13. doi:10.1016/j.cell.2006.12.018. PMID 17218247.
9. Van der Weyden L, White JK, Adams DA, Logan DW (June 2011). "The mouse genetics toolkit: revealing function and mechanism". Genome Biology. 12 (6): 224. doi:10.1186/gb-2011-12-6-224. PMC 3218837. PMID 21722353.
10. Karp NA, Baker LA, Gerdin AK, Adams NC, Ramírez-Solis R, White JK (2010). "Optimising experimental design for high-throughput phenotyping in mice: a case study". Mamm Genome. 21 (9–10): 467–76. doi:10.1007/s00335-010-9279-1. PMC 2974211. PMID 20799038.
11. Gerdin AK (2010). "The Sanger Mouse Genetics Programme: high throughput characterisation of knockout mice". Acta Ophthalmologica. 88: 925–7. doi:10.1111/j.1755-3768.2010.4142.x.
12. Wellcome Trust Sanger Institute. "MGP Phenotyping of Baz1b^{tm2a(KOMP)Wtsi}". Mouse Resources Portal. www.sanger.ac.uk. External link in |publisher= (help)
13. Wellcome Trust Sanger Institute. "Viability at Weaning Data for Baz1b". Mouse Resources Portal. www.sanger.ac.uk. External link in |publisher= (help)
14. Wellcome Trust Sanger Institute. "Weight Curves Data for Baz1b". Mouse Resources Portal. www.sanger.ac.uk. External link in |publisher= (help)
15. Wellcome Trust Sanger Institute. "Indirect Calorimetry Data for Baz1b". Mouse Resources Portal. www.sanger.ac.uk. External link in |publisher= (help)
16. Wellcome Trust Sanger Institute. "Body Composition (DEXA) Data for Baz1b". Mouse Resources Portal. www.sanger.ac.uk. External link in |publisher= (help)
17. Wellcome Trust Sanger Institute. "X-ray Imaging Data for Baz1b". Mouse Resources Portal. www.sanger.ac.uk. External link in |publisher= (help)
18. Wellcome Trust Sanger Institute. "Salmonella Challenge Data for Baz1b". Mouse Resources Portal. www.sanger.ac.uk. External link in |publisher= (help)
19. Kitagawa H, Fujiki R, Yoshimura K, Mezaki Y, Uematsu Y, Matsui D, Ogawa S, Unno K, Okubo M, Tokita A, Nakagawa T, Ito T, Ishimi Y, Nagasawa H, Matsumoto T, Yanagisawa J, Kato S (Jun 2003). "The chromatin-remodeling complex WINAC targets a nuclear receptor to promoters and is impaired in Williams syndrome". Cell. 113 (7): 905–17. doi:10.1016/S0092-8674(03)00436-7. PMID 12837248.

Further reading

• "Toward a complete human genome sequence". Genome Res. 8 (11): 1097–108. 1999. doi:10.1101/gr.8.11.1097. PMID 9847074.
• Jones MH, Hamana N, Nezu J, Shimane M (2000). "A novel family of bromodomain genes". Genomics. 63 (1): 40–5. doi:10.1006/geno.1999.6071. PMID 10662543.
• Pascual J, Martinez-Yamout M, Dyson HJ, Wright PE (2001). "Structure of the PHD zinc finger from human Williams-Beuren syndrome transcription factor". J. Mol. Biol. 304 (5): 723–9. doi:10.1006/jmbi.2000.4308. PMID 11124022.
• Bozhenok L, Wade PA, Varga-Weisz P (2002). "WSTF–ISWI chromatin remodeling complex targets heterochromatic replication foci". EMBO J. 21 (9): 2231–41. doi:10.1093/emboj/21.9.2231. PMC 125993. PMID 11980720.
• Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "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. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
• Kitagawa H, Fujiki R, Yoshimura K, et al. (2003). "The chromatin-remodeling complex WINAC targets a nuclear receptor to promoters and is impaired in Williams syndrome". Cell. 113 (7): 905–17. doi:10.1016/S0092-8674(03)00436-7. PMID 12837248.
• Hillier LW, Fulton RS, Fulton LA, et al. (2003). "The DNA sequence of human chromosome 7". Nature. 424 (6945): 157–64. doi:10.1038/nature01782. PMID 12853948.
• Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
• Beausoleil SA, Jedrychowski M, Schwartz D, et al. (2004). "Large-scale characterization of HeLa cell nuclear phosphoproteins". Proc. Natl. Acad. Sci. U.S.A. 101 (33): 12130–5. doi:10.1073/pnas.0404720101. PMC 514446. PMID 15302935.
• Poot RA, Bozhenok L, van den Berg DL, et al. (2005). "The Williams syndrome transcription factor interacts with PCNA to target chromatin remodelling by ISWI to replication foci". Nat. Cell Biol. 6 (12): 1236–44. doi:10.1038/ncb1196. PMID 15543136.
• Andersen JS, Lam YW, Leung AK, et al. (2005). "Nucleolar proteome dynamics". Nature. 433 (7021): 77–83. doi:10.1038/nature03207. PMID 15635413.
• Fujiki R, Kim MS, Sasaki Y, et al. (2005). "Ligand-induced transrepression by VDR through association of WSTF with acetylated histones". EMBO J. 24 (22): 3881–94. doi:10.1038/sj.emboj.7600853. PMC 1283952. PMID 16252006.
• Percipalle P, Fomproix N, Cavellán E, et al. (2006). "The chromatin remodelling complex WSTF–SNF2h interacts with nuclear myosin 1 and has a role in RNA polymerase I transcription". EMBO Rep. 7 (5): 525–30. doi:10.1038/sj.embor.7400657. PMC 1479564. PMID 16514417.
• Nousiainen M, Silljé HH, Sauer G, et al. (2006). "Phosphoproteome analysis of the human mitotic spindle". Proc. Natl. Acad. Sci. U.S.A. 103 (14): 5391–6. doi:10.1073/pnas.0507066103. PMC 1459365. PMID 16565220.
• Cavellán E, Asp P, Percipalle P, Farrants AK (2006). "The WSTF-SNF2h chromatin remodeling complex interacts with several nuclear proteins in transcription". J. Biol. Chem. 281 (24): 16264–71. doi:10.1074/jbc.M600233200. PMID 16603771.
• Olsen JV, Blagoev B, Gnad F, et al. (2006). "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks". Cell. 127 (3): 635–48. doi:10.1016/j.cell.2006.09.026. PMID 17081983.

External links

• BAZ1B protein, human at the US National Library of Medicine Medical Subject Headings (MeSH)

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