Biology:ALDH3B1

From HandWiki
A representation of the 3D structure of the protein myoglobin showing turquoise α-helices.
Generic protein structure example

Aldehyde dehydrogenase 3 family, member B1 also known as ALDH3B1 is an enzyme that in humans is encoded by the ALDH3B1 gene.[1][2]

Function

The aldehyde dehydrogenases are a family of isozymes that may play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. This particular gene spans about 20 kb of genomic DNA and is composed of 9 coding exons. The gene encodes a single transcript of 2.8 kb that is highly expressed in kidney and lung. The functional significance of this gene and the cellular localization of its product are presently unknown. Two transcript variants encoding different isoforms have been found for this gene.[3]

Model organisms

Model organisms have been used in the study of ALDH3B1 function. A conditional knockout mouse line called Aldh3b1tm1b(EUCOMM)Wtsi was generated at the Wellcome Trust Sanger Institute.[4] Male and female animals underwent a standardized phenotypic screen[5] to determine the effects of deletion.[6][7][8][9] Additional screens performed: - In-depth immunological phenotyping[10] - in-depth bone and cartilage phenotyping[11]

Aldh3b1 knockout mouse phenotype
Characteristic Phenotype
All data available at.[5][10][11]
Peripheral blood leukocytes 6 Weeks Normal
Haematology 6 Weeks Normal
Insulin Normal
Homozygous viability at P14 Abnormal
Homozygous Fertility Normal
Body weight Normal
Neurological assessment Normal
Grip strength Normal
Dysmorphology Normal
Indirect calorimetry Normal
Glucose tolerance test Normal
Auditory brainstem response Normal
DEXA Normal
Radiography Normal
Eye morphology Normal
Clinical chemistry Normal
Haematology 16 Weeks Normal
Peripheral blood leukocytes 16 Weeks Normal
Heart weight Normal
Salmonella infection Normal
Cytotoxic T Cell Function Normal
Epidermal Immune Composition Normal

References

  1. "Cloning of a cDNA encoding human ALDH7, a new member of the aldehyde dehydrogenase family". Gene 151 (1–2): 285–9. Dec 1994. doi:10.1016/0378-1119(94)90672-6. PMID 7828891. 
  2. "Human aldehyde dehydrogenase genes, ALDH7 and ALDH8: genomic organization and gene structure comparison". Gene 189 (1): 89–94. Apr 1997. doi:10.1016/S0378-1119(96)00839-6. PMID 9161417. 
  3. "Entrez Gene: ALDH3B1". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=221. 
  4. 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. 
  5. 5.0 5.1 "International Mouse Phenotyping Consortium". http://www.mousephenotype.org/data/search?q=Aldh3b1#fq=*:*&facet=gene. 
  6. "A conditional knockout resource for the genome-wide study of mouse gene function". Nature 474 (7351): 337–42. Jun 2011. doi:10.1038/nature10163. PMID 21677750. 
  7. "Mouse library set to be knockout". Nature 474 (7351): 262–3. Jun 2011. doi:10.1038/474262a. PMID 21677718. 
  8. "A mouse for all reasons". Cell 128 (1): 9–13. Jan 2007. doi:10.1016/j.cell.2006.12.018. PMID 17218247. 
  9. "Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes". Cell 154 (2): 452–64. 2013. doi:10.1016/j.cell.2013.06.022. PMID 23870131. 
  10. 10.0 10.1 "Infection and Immunity Immunophenotyping (3i) Consortium". http://www.immunophenotyping.org/data/search?keys=Aldh3b1&field_gene_construct_tid=All. 
  11. 11.0 11.1 "OBCD Consortium". http://www.boneandcartilage.com/. 

External links

Further reading

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