NSUN2

NSUN2
Identifiers
AliasesNSUN2, MISU, MRT5, SAKI, TRM4, NOP2/Sun RNA methyltransferase family member 2
External IDsMGI: 107252 HomoloGene: 9817 GeneCards: NSUN2
Gene location (Human)
Chr.Chromosome 5 (human)[1]
Band5p15.31Start6,599,239 bp[1]
End6,633,291 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

54888

28114

Ensembl

ENSG00000037474

ENSMUSG00000021595

UniProt

Q08J23

Q1HFZ0

RefSeq (mRNA)

NM_001193455
NM_017755

NM_145354

RefSeq (protein)

NP_001180384
NP_060225

NP_663329

Location (UCSC)Chr 5: 6.6 – 6.63 MbChr 13: 69.53 – 69.64 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

NOP2/Sun domain family, member 2 is a protein that in humans is encoded by the NSUN2 gene.[5] Alternatively spliced transcript variants encoding different isoforms have been noted for the gene.

Function

The protein is a methyltransferase that catalyzes the methylation of cytosine to 5-methylcytosine (m5C) at position 34 of intron-containing tRNA (Leu)(CAA) precursors. This modification is necessary to stabilize the anticodon-codon pairing and correctly translate the mRNA.[5]

Clinical relevance

Mutations in this gene have been found associated to cases of Dubowitz-like syndrome.[6]

Model organisms

Model organisms have been used in the study of NSUN2 function. A conditional knockout mouse line, called Nsun2tm1a(EUCOMM)Wtsi[21][22] 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.[23][24][25]

Male and female animals underwent a standardized phenotypic screen to determine the effects of deletion.[19][26] Twenty eight tests were carried out on mutant mice and fourteen significant abnormalities were observed. Homozygous mutants were subviable and had decreased body weights, length of long bones and decreased circulating glucose levels, numerous abnormal body composition, X-ray imaging, eye morphology and haematology parameters; males also had a decreased grip strength, a short upturned snout, and abnormal indirect calorimetry and plasma chemistry parameters.[19] Males (but not females) were also infertile.[19] In addition, heterozygote mutants displayed premature hair follicle exogen.[19]

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000037474 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000021595 - Ensembl, May 2017
  3. ↑ "Human PubMed Reference:".
  4. ↑ "Mouse PubMed Reference:".
  5. 1 2 "NOP2/Sun domain family, member 2". Retrieved 2011-12-04.
  6. ↑ Martinez FJ, Lee JH, Lee JE, Blanco S, Nickerson E, Gabriel S, Frye M, Al-Gazali L, Gleeson JG (June 2012). "Whole exome sequencing identifies a splicing mutation in NSUN2 as a cause of a Dubowitz-like syndrome". J. Med. Genet. 49 (6): 380–5. doi:10.1136/jmedgenet-2011-100686. PMC 4771841. PMID 22577224.
  7. ↑ "Body weight data for Nsun2". Wellcome Trust Sanger Institute.
  8. ↑ "Grip strength data for Nsun2". Wellcome Trust Sanger Institute.
  9. ↑ "Dysmorphology data for Nsun2". Wellcome Trust Sanger Institute.
  10. ↑ "Indirect calorimetry data for Nsun2". Wellcome Trust Sanger Institute.
  11. ↑ "Glucose tolerance test data for Nsun2". Wellcome Trust Sanger Institute.
  12. ↑ "DEXA data for Nsun2". Wellcome Trust Sanger Institute.
  13. ↑ "Radiography data for Nsun2". Wellcome Trust Sanger Institute.
  14. ↑ "Eye morphology data for Nsun2". Wellcome Trust Sanger Institute.
  15. ↑ "Clinical chemistry data for Nsun2". Wellcome Trust Sanger Institute.
  16. ↑ "Haematology data for Nsun2". Wellcome Trust Sanger Institute.
  17. ↑ "Salmonella infection data for Nsun2". Wellcome Trust Sanger Institute.
  18. ↑ "Citrobacter infection data for Nsun2". Wellcome Trust Sanger Institute.
  19. 1 2 3 4 5 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.
  20. ↑ Mouse Resources Portal, Wellcome Trust Sanger Institute.
  21. ↑ "International Knockout Mouse Consortium".
  22. ↑ "Mouse Genome Informatics".
  23. ↑ Skarnes, W. C.; Rosen, B.; West, A. P.; Koutsourakis, M.; Bushell, W.; Iyer, V.; Mujica, A. O.; Thomas, M.; Harrow, J.; Cox, T.; Jackson, D.; Severin, J.; Biggs, P.; Fu, J.; Nefedov, M.; De Jong, P. J.; Stewart, A. F.; Bradley, A. (2011). "A conditional knockout resource for the genome-wide study of mouse gene function". Nature. 474 (7351): 337–342. doi:10.1038/nature10163. PMC 3572410. PMID 21677750.
  24. ↑ Dolgin E (2011). "Mouse library set to be knockout". Nature. 474 (7351): 262–3. doi:10.1038/474262a. PMID 21677718.
  25. ↑ Collins FS, Rossant J, Wurst W (2007). "A Mouse for All Reasons". Cell. 128 (1): 9–13. doi:10.1016/j.cell.2006.12.018. PMID 17218247.
  26. ↑ van der Weyden L, White JK, Adams DJ, Logan DW (2011). "The mouse genetics toolkit: revealing function and mechanism". Genome Biol. 12 (6): 224. doi:10.1186/gb-2011-12-6-224. PMC 3218837. PMID 21722353.

Further reading

  • Frye M, Dragoni I, Chin SF, Spiteri I, Kurowski A, Provenzano E, Green A, Ellis IO, Grimmer D, Teschendorff A, Zouboulis CC, Caldas C, Watt FM (2010). "Genomic gain of 5p15 leads to over-expression of Misu (NSUN2) in breast cancer". Cancer Letters. 289 (1): 71–80. doi:10.1016/j.canlet.2009.08.004. PMID 19740597.
  • Hussain S, Benavente SB, Nascimento E, Dragoni I, Kurowski A, Gillich A, Humphreys P, Frye M (2009). "The nucleolar RNA methyltransferase Misu (NSun2) is required for mitotic spindle stability". The Journal of Cell Biology. 186 (1): 27–40. doi:10.1083/jcb.200810180. PMC 2712989. PMID 19596847.
  • Sakita-Suto S, Kanda A, Suzuki F, Sato S, Takata T, Tatsuka M (2007). "Aurora-B Regulates RNA Methyltransferase NSUN2". Molecular Biology of the Cell. 18 (3): 1107–1117. doi:10.1091/mbc.E06-11-1021. PMC 1805108. PMID 17215513.


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