NSUN2

NSUN2
Identifiers
Aliases	NSUN2 , MISU, MRT5, SAKI, TRM4, NOP2/Sun RNA methyltransferase family member 2, NOP2/Sun RNA methyltransferase 2
External IDs	OMIM: 610916 MGI: 107252 HomoloGene: 9817 GeneCards: NSUN2
Gene location (Human) Chr. Chromosome 5 (human) [1] Band 5p15.31 Start 6,599,239 bp [1] End 6,633,291 bp [1]
Gene location (Mouse) Chr. Chromosome 13 (mouse) [2] Band 13 B3|13 35.55 cM Start 69,681,865 bp [2] End 69,783,899 bp [2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in right uterine tube secondary oocyte right lobe of liver skin of abdomen appendix lymph node pancreatic epithelial cell spleen body of pancreas left uterine tube Top expressed in otic placode saccule primitive streak abdominal wall hair follicle seminiferous tubule somite skin of back yolk sac uterus More reference expression data BioGPS n/a
Gene ontology Molecular function methyltransferase activity transferase activity tRNA binding tRNA (cytosine-5-)-methyltransferase activity RNA binding Cellular component cytoplasm chromatoid body spindle nucleoplasm nucleolus cytoskeleton nucleus Biological process tRNA methylation meiotic cell cycle checkpoint signaling cell division tRNA modification methylation spermatid development cell cycle tRNA processing hair follicle maturation Sources:Amigo / QuickGO
Orthologs Species Human Mouse 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 Mb Chr 13: 69.68 – 69.78 Mb PubMed search [3] [4]
Wikidata
View/Edit Human View/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] NSUN2 is also localized on mitochondria and is capable of introducing post-transcriptional modifications in mitochondrial tRNAs. ^{[6] [7]}

Clinical relevance

Mutations in this gene have been found associated to cases of Dubowitz-like syndrome. ^[8]

Model organisms

Nsun2 knockout mouse phenotype

Characteristic	Phenotype
Homozygote viability	Abnormal
Recessive lethal study	Normal
Homozygous Fertility	Abnormal
Body weight	Abnormal [9]
Anxiety	Normal
Neurological assessment	Normal
Grip strength	Abnormal [10]
Hot plate	Normal
Dysmorphology	Abnormal [11]
Indirect calorimetry	Abnormal [12]
Glucose tolerance test	Abnormal [13]
Auditory brainstem response	Normal
DEXA	Abnormal [14]
Radiography	Abnormal [15]
Body temperature	Normal
Eye morphology	Abnormal [16]
Clinical chemistry	Abnormal [17]
Plasma immunoglobulins	Normal
Haematology	Abnormal [18]
Peripheral blood lymphocytes	Normal
Micronucleus test	Normal
Heart weight	Normal
Tail epidermis wholemount	Normal
Skin Histopathology	Abnormal
Brain histopathology	Normal
MicroCT & Quantitative Faxitron	Abnormal
Salmonella infection	Normal [19]
Citrobacter infection	Normal [20]
All tests and analysis from [21] [22]

Model organisms have been used in the study of NSUN2 function. A conditional knockout mouse line, called Nsun2^{tm1a(EUCOMM)Wtsi [23] [24]} 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. ^{[25] [26] [27]}

Male and female animals underwent a standardized phenotypic screen to determine the effects of deletion. ^{[21] [28]} 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. ^[21] Males (but not females) were also infertile. ^[21] In addition, heterozygote mutants displayed premature hair follicle exogen. ^[21]

References

1. GRCh38: Ensembl release 89: ENSG00000037474 - Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000021595 - Ensembl, May 2017
3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
5. "NOP2/Sun domain family, member 2" . Retrieved 2011-12-04.
6. Shinoda S, Kitagawa S, Nakagawa S, Wei FY, Tomizawa K, Araki K, et al. (July 2019). "Mammalian NSUN2 introduces 5-methylcytidines into mitochondrial tRNAs". Nucleic Acids Research. 47 (16): 8734–8745. doi:10.1093/nar/gkz575. PMC   6895283 . PMID   31287866.
7. Van Haute L, Lee SY, McCann BJ, Powell CA, Bansal D, Vasiliauskaitė L, et al. (July 2019). "NSUN2 introduces 5-methylcytosines in mammalian mitochondrial tRNAs". Nucleic Acids Research. 47 (16): 8720–8733. doi:10.1093/nar/gkz559. PMC   6822013 . PMID   31276587.
8. Martinez FJ, Lee JH, Lee JE, Blanco S, Nickerson E, Gabriel S, et al. (June 2012). "Whole exome sequencing identifies a splicing mutation in NSUN2 as a cause of a Dubowitz-like syndrome". Journal of Medical Genetics. 49 (6): 380–5. doi:10.1136/jmedgenet-2011-100686. PMC   4771841 . PMID   22577224.
9. "Body weight data for Nsun2". Wellcome Trust Sanger Institute.
10. "Grip strength data for Nsun2". Wellcome Trust Sanger Institute.
11. "Dysmorphology data for Nsun2". Wellcome Trust Sanger Institute.
12. "Indirect calorimetry data for Nsun2". Wellcome Trust Sanger Institute.
13. "Glucose tolerance test data for Nsun2". Wellcome Trust Sanger Institute.
14. "DEXA data for Nsun2". Wellcome Trust Sanger Institute.
15. "Radiography data for Nsun2". Wellcome Trust Sanger Institute.
16. "Eye morphology data for Nsun2". Wellcome Trust Sanger Institute.
17. "Clinical chemistry data for Nsun2". Wellcome Trust Sanger Institute.
18. "Haematology data for Nsun2". Wellcome Trust Sanger Institute.
19. "Salmonella infection data for Nsun2". Wellcome Trust Sanger Institute.
20. "Citrobacter infection data for Nsun2". Wellcome Trust Sanger Institute.
21. 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. S2CID   85911512.
22. Mouse Resources Portal, Wellcome Trust Sanger Institute.
23. "International Knockout Mouse Consortium".
24. "Mouse Genome Informatics".
25. Skarnes WC, Rosen B, West AP, Koutsourakis M, Bushell W, Iyer V, et al. (June 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.
26. Dolgin E (June 2011). "Mouse library set to be knockout". Nature. 474 (7351): 262–3. doi: 10.1038/474262a . PMID   21677718.
27. 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. S2CID   18872015.
28. van der Weyden L, White JK, Adams DJ, 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.

Further reading

• Frye M, Dragoni I, Chin SF, Spiteri I, Kurowski A, Provenzano E, et al. (March 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, et al. (July 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 (March 2007). "Aurora-B regulates RNA methyltransferase NSUN2". Molecular Biology of the Cell. 18 (3): 1107–17. doi:10.1091/mbc.E06-11-1021. PMC   1805108 . PMID   17215513.