BBX (gene)

Jump to navigation Jump to search
VALUE_ERROR (nil)
Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

n/a

n/a

RefSeq (protein)

n/a

n/a

Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

HMG box transcription factor BBX also known as bobby sox homolog or HMG box-containing protein 2 is a protein that in humans is encoded by the BBX gene.[1]

Model organisms

Model organisms have been used in the study of BBX function. A conditional knockout mouse line, called Bbxtm1a(EUCOMM)Wtsi[10][11] 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.[12][13][14]

Male and female animals underwent a standardized phenotypic screen to determine the effects of deletion.[8][15] Twenty six tests were carried out on homozygous mutant adult mice and four significant abnormalities were observed.[8] A study of body composition found decreases in bone mineral density and content, and a reduction in body length in female mice, while mutants of both sexes showed a reduction in lean body mass. Radiography found that males had abnormal teeth morphology. Females had a decreased heart weight, and both sexes had reduced IgA levels in their plasma.[8]

References

  1. "Entrez Gene: bobby sox homolog (Drosophila)". Retrieved 2011-08-30.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  2. "DEXA data for Bbx". Wellcome Trust Sanger Institute.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  3. "Radiography data for Bbx". Wellcome Trust Sanger Institute.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  4. "Haematology data for Bbx". Wellcome Trust Sanger Institute.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  5. "Heart weight data for Bbx". Wellcome Trust Sanger Institute.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  6. "Salmonella infection data for Bbx". Wellcome Trust Sanger Institute.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  7. "Citrobacter infection data for Bbx". Wellcome Trust Sanger Institute.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  8. 8.0 8.1 8.2 8.3 Gerdin AK (2010). "The Sanger Mouse Genetics Programme: High throughput characterisation of knockout mice". Acta Ophthalmologica. 88 (S248). doi:10.1111/j.1755-3768.2010.4142.x.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  9. Mouse Resources Portal, Wellcome Trust Sanger Institute.
  10. "International Knockout Mouse Consortium".<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  11. "Mouse Genome Informatics".<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  12. Skarnes WC, Rosen B, West AP, Koutsourakis M, Bushell W, Iyer V, Mujica AO, Thomas M, Harrow J, Cox T, Jackson D, Severin J, Biggs P, Fu J, Nefedov M, de Jong PJ, Stewart AF, Bradley A (Jun 2011). "A conditional knockout resource for the genome-wide study of mouse gene function". Nature. 474 (7351): 337–42. doi:10.1038/nature10163. PMC 3572410. PMID 21677750.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  13. Dolgin E (Jun 2011). "Mouse library set to be knockout". Nature. 474 (7351): 262–3. doi:10.1038/474262a. PMID 21677718.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  14. Collins FS, Rossant J, Wurst W (Jan 2007). "A mouse for all reasons". Cell. 128 (1): 9–13. doi:10.1016/j.cell.2006.12.018. PMID 17218247.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  15. van der Weyden L, White JK, Adams DJ, Logan DW (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.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>

External links

Further reading

<templatestyles src="Refbegin/styles.css" />

  • Caporaso N, Gu F, Chatterjee N, Sheng-Chih J, Yu K, Yeager M, Chen C, Jacobs K, Wheeler W, Landi MT, Ziegler RG, Hunter DJ, Chanock S, Hankinson S, Kraft P, Bergen AW (2009). "Genome-wide and candidate gene association study of cigarette smoking behaviors". PLOS ONE. 4 (2): e4653. doi:10.1371/journal.pone.0004653. PMC 2644817. PMID 19247474.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  • Wang HY, Peng G, Guo Z, Shevach EM, Wang RF (Mar 2005). "Recognition of a new ARTC1 peptide ligand uniquely expressed in tumor cells by antigen-specific CD4+ regulatory T cells". Journal of Immunology. 174 (5): 2661–70. doi:10.4049/jimmunol.174.5.2661. PMID 15728473.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  • Trynka G, Zhernakova A, Romanos J, Franke L, Hunt KA, Turner G, Bruinenberg M, Heap GA, Platteel M, Ryan AW, de Kovel C, Holmes GK, Howdle PD, Walters JR, Sanders DS, Mulder CJ, Mearin ML, Verbeek WH, Trimble V, Stevens FM, Kelleher D, Barisani D, Bardella MT, McManus R, van Heel DA, Wijmenga C (Aug 2009). "Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-kappaB signalling". Gut. 58 (8): 1078–83. doi:10.1136/gut.2008.169052. PMID 19240061.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  • Bonaldo MF, Lennon G, Soares MB (Sep 1996). "Normalization and subtraction: two approaches to facilitate gene discovery". Genome Research. 6 (9): 791–806. doi:10.1101/gr.6.9.791. PMID 8889548.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  • Andersson B, Wentland MA, Ricafrente JY, Liu W, Gibbs RA (Apr 1996). "A "double adaptor" method for improved shotgun library construction". Analytical Biochemistry. 236 (1): 107–13. doi:10.1006/abio.1996.0138. PMID 8619474.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  • Sánchez-Díaz A, Blanco MA, Jones N, Moreno S (Sep 2001). "HBP2: a new mammalian protein that complements the fission yeast MBF transcription complex". Current Genetics. 40 (2): 110–8. doi:10.1007/s002940100241. PMID 11680820.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>