Biology:CAPRIN2

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

caprin family member 2, also known as CAPRIN2, is a human gene.[1]

The protein encoded by this gene may be involved in the transitioning of erythroblasts from a highly proliferative state to a terminal phase of differentiation. High level expression of the encoded protein can lead to apoptosis. Several transcript variants encoding different isoforms have been found for this gene.[1]

Model organisms

Model organisms have been used in the study of CAPRIN2 function. A conditional knockout mouse line, called Caprin2tm1a(EUCOMM)Wtsi[5][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.[3][10] Twenty two tests were carried out on mutant mice, however no significant abnormalities were observed.[3]

References

  1. 1.0 1.1 "Entrez Gene: caprin family member 2". https://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=retrieve&list_uids=65981. Retrieved 2011-08-30. 
  2. "Citrobacter infection data for Caprin2". Wellcome Trust Sanger Institute. http://www.sanger.ac.uk/mouseportal/phenotyping/MAXJ/citrobacter-challenge/. 
  3. 3.0 3.1 3.2 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. 
  4. Mouse Resources Portal, Wellcome Trust Sanger Institute.
  5. "International Knockout Mouse Consortium". http://www.knockoutmouse.org/martsearch/search?query=Caprin2. 
  6. "Mouse Genome Informatics". http://www.informatics.jax.org/searchtool/Search.do?query=MGI:4432518. 
  7. Skarnes, W. C.; Rosen, B.; West, A. P.; Koutsourakis, M.; Bushell, W.; Iyer, V.; Mujica, A. O.; Thomas, M. et al. (2011). "A conditional knockout resource for the genome-wide study of mouse gene function". Nature 474 (7351): 337–342. doi:10.1038/nature10163. PMID 21677750. 
  8. Dolgin E (June 2011). "Mouse library set to be knockout". Nature 474 (7351): 262–3. doi:10.1038/474262a. PMID 21677718. 
  9. "A mouse for all reasons". Cell 128 (1): 9–13. January 2007. doi:10.1016/j.cell.2006.12.018. PMID 17218247. 
  10. "The mouse genetics toolkit: revealing function and mechanism.". Genome Biol 12 (6): 224. 2011. doi:10.1186/gb-2011-12-6-224. PMID 21722353. 

External links

Further reading