NOP2/Sun Domain Family, Member 2 (NSUN2)

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TRM4; Misu; SAKI; tRNA Methyltransferase 4; Myc-Induced SUN-Domain-Containing Protein; tRNA (cytosine(34)-C(5))-methyltransferase; NOL1/NOP2/Sun domain family member 2

NOP2/Sun Domain Family, Member 2 (NSUN2)
NSUN2 encodes a methyltransferase that catalyzes the intron-dependent formation of 5-methylcytosine at C34 of tRNA-leu(CAA). The full-length human protein contains 767 amino acids and has a SUN domain. One variant lacks exon 3, resulting in a 35-amino acid deletion, and the other 2 variants encode smaller proteins lacking the SUN domain. RT-PCR detected predominant expression of full-length MISU and lower expression of the MISU variant lacking exon 3 in all human cell lines examined. Northern blot analysis detected ubiquitous expression of Misu in mouse tissues. MISU was distributed throughout the nucleus during S phase, when the number and size of nucleoli increase. In G2 phase, some MISU was detected in cytoplasmic vesicles, and MISU localized to the spindle during mitosis.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant NOP2/Sun Domain Family, Member 2 (NSUN2) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to NOP2/Sun Domain Family, Member 2 (NSUN2) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to NOP2/Sun Domain Family, Member 2 (NSUN2) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for NOP2/Sun Domain Family, Member 2 (NSUN2) CLIA Kit Customized Service Offer
n/a ELISA Kit for NOP2/Sun Domain Family, Member 2 (NSUN2) ELISA Kit Customized Service Offer

Organism species: Mus musculus (Mouse)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant NOP2/Sun Domain Family, Member 2 (NSUN2) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to NOP2/Sun Domain Family, Member 2 (NSUN2) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to NOP2/Sun Domain Family, Member 2 (NSUN2) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for NOP2/Sun Domain Family, Member 2 (NSUN2) CLIA Kit Customized Service Offer
n/a ELISA Kit for NOP2/Sun Domain Family, Member 2 (NSUN2) ELISA Kit Customized Service Offer

Organism species: Rattus norvegicus (Rat)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant NOP2/Sun Domain Family, Member 2 (NSUN2) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to NOP2/Sun Domain Family, Member 2 (NSUN2) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to NOP2/Sun Domain Family, Member 2 (NSUN2) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for NOP2/Sun Domain Family, Member 2 (NSUN2) CLIA Kit Customized Service Offer
n/a ELISA Kit for NOP2/Sun Domain Family, Member 2 (NSUN2) ELISA Kit Customized Service Offer
  1. "Aurora-B regulates RNA methyltransferase NSUN2."Mol. Biol. Cell 18:1107-1117(2007) [PubMed] [Europe PMC] [Abstract]
  2. "Complete sequencing and characterization of 21,243 full-length human cDNAs." Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract]
  3. "The DNA sequence and comparative analysis of human chromosome 5." Nature 431:268-274(2004) [PubMed] [Europe PMC] [Abstract]
  4. "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
  5. "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks."Cell 127:635-648(2006) [PubMed] [Europe PMC] [Abstract]
  6. "A probability-based approach for high-throughput protein phosphorylation analysis and site localization."Nat. Biotechnol. 24:1285-1292(2006) [PubMed] [Europe PMC] [Abstract]
  7. "Identification of human tRNA:m5C methyltransferase catalysing intron-dependent m5C formation in the first position of the anticodon of the pre-tRNA Leu (CAA)."Nucleic Acids Res. 34:6034-6043(2006) [PubMed] [Europe PMC] [Abstract]
  8. "Combining protein-based IMAC, peptide-based IMAC, and MudPIT for efficient phosphoproteomic analysis."J. Proteome Res. 7:1346-1351(2008) [PubMed] [Europe PMC] [Abstract]
  9. "A quantitative atlas of mitotic phosphorylation."Proc. Natl. Acad. Sci. U.S.A. 105:10762-10767(2008) [PubMed] [Europe PMC] [Abstract]
  10. "Lys-N and trypsin cover complementary parts of the phosphoproteome in a refined SCX-based approach."Anal. Chem. 81:4493-4501(2009) [PubMed] [Europe PMC] [Abstract]
  11. "The nucleolar RNA methyltransferase Misu (NSun2) is required for mitotic spindle stability."J. Cell Biol. 186:27-40(2009) [PubMed] [Europe PMC] [Abstract]
  12. "Quantitative phosphoproteomic analysis of T cell receptor signaling reveals system-wide modulation of protein-protein interactions."Sci. Signal. 2:RA46-RA46(2009) [PubMed] [Europe PMC] [Abstract]
  13. "Quantitative phosphoproteomics reveals widespread full phosphorylation site occupancy during mitosis."Sci. Signal. 3:RA3-RA3(2010) [PubMed] [Europe PMC] [Abstract]
  14. "Initial characterization of the human central proteome."BMC Syst. Biol. 5:17-17(2011) [PubMed] [Europe PMC] [Abstract]
  15. "The first identification of lysine malonylation substrates and its regulatory enzyme."Mol. Cell. Proteomics 10:M111.012658.01-M111.012658.12(2011) [PubMed] [Europe PMC] [Abstract]
  16. "System-wide temporal characterization of the proteome and phosphoproteome of human embryonic stem cell differentiation."Sci. Signal. 4:RS3-RS3(2011) [PubMed] [Europe PMC] [Abstract]
  17. "Mutations in NSUN2 cause autosomal-recessive intellectual disability."Am. J. Hum. Genet. 90:847-855(2012) [PubMed] [Europe PMC] [Abstract]
  18. "The human tRNA m (5) C methyltransferase Misu is multisite-specific."RNA Biol. 9:1331-1338(2012) [PubMed] [Europe PMC] [Abstract]
  19. "An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome."J. Proteomics 96:253-262(2014) [PubMed] [Europe PMC] [Abstract]
  20. "Mutation in NSUN2, which encodes an RNA methyltransferase, causes autosomal-recessive intellectual disability."Am. J. Hum. Genet. 90:856-863(2012) [PubMed] [Europe PMC] [Abstract]