Host Protein General Information (ID: PT1180)
  Protein Name
tRNA methyltransferase 10 homolog C (TRMT10C)
  Gene Name
TRMT10C
  Host Species
Homo sapiens
  Uniprot Entry Name
TM10C_HUMAN
  Protein Families
Class IV-like SAM-binding methyltransferase superfamily
  EC Number
2.1.1.-; 2.1.1.218; 2.1.1.221
  Subcellular Location
Mitochondrion matrix; mitochondrion nucleoid
  External Link
NCBI Gene ID
54931
Uniprot ID
Q7L0Y3
Ensembl ID
ENSG00000174173
HGNC ID
HGNC:26022
  Function in Host
Mitochondrial tRNA N (1) -methyltransferase involved inmitochondrial tRNA maturation. Component of mitochondrialribonuclease P, a complex composed of TRMT10C/MRPP1, HSD17B10/MRPP2 andPRORP/MRPP3, which cleaves tRNA molecules in their 5'-ends. Together with HSD17B10/MRPP2, forms a subcomplex ofthe mitochondrial ribonuclease P, named MRPP1-MRPP2 subcomplex, whichdisplays functions that are independent of the ribonuclease P activity. The MRPP1-MRPP2 subcomplexcatalyzes the formation of N (1) -methylguanine and N (1) -methyladenine atposition 9 (m1G9 and m1A9, respectively) in tRNAs; TRMT10C/MRPP1 actingas the catalytic N (1) -methyltransferase subunit. TheMRPP1-MRPP2 subcomplex also acts as a tRNA maturation platform:following 5'-end cleavage by the mitochondrial ribonuclease P complex, the MRPP1-MRPP2 subcomplex enhances the efficiency of 3'-processingcatalyzed by ELAC2, retains the tRNA product after ELAC2 processing andpresents the nascent tRNA to the mitochondrial CCA tRNAnucleotidyltransferase TRNT1 enzyme. In addition totRNA N (1) -methyltransferase activity, TRMT10C/MRPP1 also acts as a mRNAN (1) -methyltransferase by mediating methylation of adenosine residuesat the N (1) position of MT-ND5 mRNA. Associates withmitochondrial DNA complexes at the nucleoids to initiate RNA processingand ribosome assembly. [1-5]
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  3D Structure

Function of This Protein During Virus Infection
Virus NameSARS-COV-2 Protein Function Anti-viral [6]
Infected TissueLung Infection Time7-9 Days
Infected CellCalu-3 Cells (Human epithelial cell line) Cellosaurus IDCVCL_0609 
Method DescriptionTo detect the role of host protein TRMT10C in viral infection, TRMT10C protein knockdown Calu-3 Cells were infected with SARS-COV-2 for 7 - 9 Days , and the effects on infection was detected through CRISPR-based genome-wide gene-knockout screen.
ResultsIt is reported that knockout of TRMT10C increases SARS-CoV-2 RNA levels compared with control group.

 Full List of Virus RNA Interacting with This Protien
            RNA Region: Not Specified Virus Region (hCoV-19/England/02/2020 )
              RNA Region Details RNA Info Click to show the detail information of this RNA binding region [7]
              Strains Name
hCoV-19/England/02/2020
              Strains Family
Beta (B.1.351)
              RNA Binding Region
Not Specified Virus Region
              Virus Name
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)
              Infection Cells Calu-3 cells (Human lung cancer cell)  (CVCL_0609 )
              Cell Originated Tissue Lung
              Infection Time 24 h
              Interaction Score P-adjust = 0.030
              Method Description UV protein-RNA crosslinking; RNA interactome capture (cRIC); RNA antisense purification coupled with mass spectrometry (RAP-MS)

Differential Gene Expression During SARS-COV-2 Infection
GEO Accession: GSE152641
Sample Type: Blood
Samples Details: Healthy Control: 24; COVID-19: 62
Platform: GPL24676 Illumina NovaSeq 6000
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GEO Accession: GSE162835
Sample Type: Nasopharyngeal Swabs
Samples Details: COVID-19 (Mild Symptoms): 37; COVID-19 (Moderate Symptoms): 10; COVID-19 (Severe Symptoms): 3
Platform: GPL24676 Illumina NovaSeq 6000
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GEO Accession: GSE175779
Sample Type: Human Bronchial Epithelial Cells
Samples Details: Healthy Control: 4 (0, 24, 48, 72 and 96 h); COVID-19: 4 (24, 48, 72 and 96 h)
Platform: GPL18573 Illumina NextSeq 500
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Protein Sequence Information
MAAFLKMSVSVNFFRPFTRFLVPFTLHRKRNNLTILQRYMSSKIPAVTYPKNESTPPSEELELDKWKTTMKSSVQEECVSTISSSKDEDPLAATREFIEMWRLLGREVPEHITEEELKTLMECVSNTAKKKYLKYLYTKEKVKKARQIKKEMKAAAREEAKNIKLLETTEEDKQKNFLFLRLWDRNMDIAMGWKGAQAMQFGQPLVFDMAYENYMKRKELQNTVSQLLESEGWNRRNVDPFHIYFCNLKIDGALHRELVKRYQEKWDKLLLTSTEKSHVDLFPKDSIIYLTADSPNVMTTFRHDKVYVIGSFVDKSMQPGTSLAKAKRLNLATECLPLDKYLQWEIGNKNLTLDQMIRILLCLKNNGNWQEALQFVPKRKHTGFLEISQHSQEFINRLKKAKT
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References
1 Involvement of human ELAC2 gene product in 3 end processing of mitochondrial tRNAs. RNA Biol. Jul-Aug 2011;8(4):616-26.
2 The MRPP1/MRPP2 complex is a tRNA-maturation platform in human mitochondria. Nucleic Acids Res. 2017 Dec 1;45(21):12469-12480.
3 Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies. Am J Hum Genet. 2016 May 5;98(5):993-1000.
4 A subcomplex of human mitochondrial RNase P is a bifunctional methyltransferase--extensive moonlighting in mitochondrial tRNA biogenesis. Nucleic Acids Res. 2012 Dec;40(22):11583-93.
5 RNase P without RNA: identification and functional reconstitution of the human mitochondrial tRNA processing enzyme. Cell. 2008 Oct 31;135(3):462-74.
6 Genome-wide CRISPR screens identify GATA6 as a proviral host factor for SARS-CoV-2 via modulation of ACE2. Nat Commun. 2022 Apr 25;13(1):2237.
7 Global analysis of protein-RNA interactions in SARS-CoV-2-infected cells reveals key regulators of infection. Mol Cell. 2021 Jul 1;81(13):2851-2867.e7.