Citations for
1GABPA, TFB1M
GABP transcription factor (nuclear respiratory factor 2) is required for mitochondrial biogenesis.
Yang ZF, Drumea K, Mott S, Wang J, Rosmarin AG.
Mol Cell Biol 34(17):3194-201. doi: 10.1128/MCB.00492-12. Epub 2014 Jun 23. 2014
2E2F1, TFB1M
Mitochondrial stress engages E2F1 apoptotic signaling to cause deafness.
Raimundo N, Song L, Shutt TE, McKay SE, Cotney J, Guan MX, Gilliland TC, Hohuan D, Santos-Sacchi J, Shadel GS.
Cell 148(4):716-26. doi: 10.1016/j.cell.2011.12.027. 2012
3TFB1M
A common variant in TFB1M is associated with reduced insulin secretion and increased future risk of type 2 diabetes.
Koeck T, Olsson AH, Nitert MD, Sharoyko VV, Ladenvall C, Kotova O, Reiling E, Rönn T, Parikh H, Taneera J, Eriksson JG, Metodiev MD, Larsson NG, Balhuizen A, Luthman H, Stančáková A, Kuusisto J, Laakso M, Poulsen P, Vaag A, Groop L, Lyssenko V, Mulder H, Ling C.
Cell Metab 13(1):80-91. doi: 10.1016/j.cmet.2010.12.007. 2011
4MTERF1, TFB1M, TFB2M
Training response of mitochondrial transcription factors in human skeletal muscle.
Norrbom J, Wallman SE, Gustafsson T, Rundqvist H, Jansson E, Sundberg CJ.
Acta Physiol (Oxf) 198(1):71-9. Epub 2009 Aug 13. 2010
5TFB1M, TFB2M
Training response of mitochondrial transcription factors in human skeletal muscle.
Norrbom J, Wallman SE, Gustafsson T, Rundqvist H, Jansson E, Sundberg CJ.
Acta Physiol (Oxf) 198(1):71-9. doi: 10.1111/j.1748-1716.2009.02030.x. Epub 2009 Aug 13. 2010
6TFB1M, TFB2M
Elucidation of separate, but collaborative functions of the rRNA methyltransferase-related human mitochondrial transcription factors B1 and B2 in mitochondrial biogenesis reveals new insight into maternally inherited deafness.
Cotney J, McKay SE, Shadel GS.
Hum Mol Genet 18(14):2670-82. Epub 2009 May 5. 2009
7TFB1M, TFB2M
Relative abundance of the human mitochondrial transcription system and distinct roles for h-mtTFB1 and h-mtTFB2 in mitochondrial biogenesis and gene expression.
Cotney J, Wang Z, Shadel GS.
Nucleic Acids Res 35(12):4042-54. Epub 2007 Jun 8. 2007
8TFB1M, TFB2M
Evidence for an early gene duplication event in the evolution of the mitochondrial transcription factor B family and maintenance of rRNA methyltransferase activity in human mtTFB1 and mtTFB2.
Cotney J, Shadel GS.
J Mol Evol 63(5):707-17. Epub 2006 Oct 6. 2006
9TFB1M, TFB2M
Control of mitochondrial transcription specificity factors (TFB1M and TFB2M) by nuclear respiratory factors (NRF-1 and NRF-2) and PGC-1 family coactivators.
Gleyzer N, Vercauteren K, Scarpulla RC.
Mol Cell Biol 25(4):1354-66. 2005
10TFB1M
Human mitochondrial transcription factor B1 as a modifier gene for hearing loss associated with the mitochondrial A1555G mutation.
Bykhovskaya Y, Mengesha E, Wang D, Yang H, Estivill X, Shohat M, Fischel-Ghodsian N.
Mol Genet Metab 82(1):27-32. 2004
11TFB1M
Human mitochondrial transcription factor B1 as a modifier gene for hearing loss associated with the mitochondrial A1555G mutation.
Bykhovskaya Y, Mengesha E, Wang D, Yang H, Estivill X, Shohat M, Fischel-Ghodsian N.
Mol Genet Metab 82(1):27-32. 2004
12TFB1M
A human mitochondrial transcription factor is related to RNA adeninemethyltransferases and binds S-adenosylmethionine.
McCulloch V, Seidel-Rogol BL, Shadel GS.
Mol Cell Biol 22(4):1116-25. 2002
13ADIPOR1, AIG1, AMDHD2, ANKHD1, ANKRD20A1, ANKRD27, ANKRD32, APH1A, APH1B, APIP, APOLD1, ARS2, ASCC1, ATXN10, BOLA1, C10orf10, C14orf166, C19orf56, C20orf109, C20orf4, C2orf14, C2orf16, C6orf60, C6orf62, CALCOCO1, CAMKK1, CCDC113, CCDC53, CCDC9, CCNB2, CD99L2, CDK5RAP1, CDK5RAP1, CGI-96, CHMP5, CHPF, CIAO2B, CLIC4, CLPB, COPZ1, COQ4, COQ6, CRELD1, CUTC, CYBRD1, DDX47, DERA, DHRS7, DHRS7B, DHRS7B, DPH5, DTNB, DYNC1LI2, EEF1AKNMT, ELOVL1, EMC9, ERGIC3, ESPN, EXOSC1, EXOSC3, FAHD2A, FAM108B1, FAM18B, FAM32A, FAM82B, FCF1, FIP1L1, FLYWCH1, FYTTD1, GABARAPL1, GET4, GLOD4, GLRX2, GOLT1B, GOLT1B, GPR89A, GPS2, GRIPAP1, HDDC2, HDGFRP3, HIGD1A, IER3IP1, IFT52, ISOC1, KIF18A, KIF20B, KIRREL2, KL3, KLC2, LACTB2, LHX6, LMAN2L, LUC7L2, MAF1, MAGMAS, MECR, MED23, MED31, MEMO, METTL9, MIS12, MOABHD5, MOB4, MPC1, MRPL11, MRPL2, MRPL4, MRPL48, MRPS15, MRPS16, MRPS16P2, MRPS18C, MRPS23, MRPS33, MTCH1, MTERF3, MTO1, MYCBPAP, NCALD, NCIE2, NDUFAF1, NELF, NELFB, NFU1, NMD3, NOSIP, NRBF2, NRIP2, NRIP2, NRSN2, NUDT12, OTUD6B, PARVB, PCBD2, PHF20L1, PIGT, PMFBP1, PNAS-4, PRPF31, PRSS23, PTRH2, QRSL1, RBMX2, RGMA, RGMB, RNF103-CHMP3, RNF123, RNF146, RRNAD1, RRP15, RWDD1, RWDD3, SAMHD1, SAMM50, SCCPDH, SECISBP2, SEMA4F, SERBP1, SERBP1, SERP1, SH3BP5L, SIDT2, SLC25A24, SLC25A39, SLC35C2, SLC37A3, SLC41A2, SLC6A16, SLMO2, SMC6, SPEF1, SQRDL, STARD10, STMN2, SYF2, TARDBP, TBC1D3, TBL2, TFB1M, TFIP11, THAP4, THAP4, TIGD6, TIMMDC1, TMED5, TMED7, TMEM47, TPPP3, TRAF7, TRAPPC12, TRAPPC4, TRMT6, TRNT1, TSC22D3, TSPAN14, TWF2, UBE1DC1, UBE2J1, UCHL5, UNC50, USP39, UTP11L, VPS36, WDR37, WDR50, WDR91, WSB1, YARS2, YIPF3, YPEL5, ZC2HC1A, ZC3H13, ZDHHC9, ZMYND12, ZMYND15, ZRANB3
Identification of novel human genes evolutionarily conserved in Caenorhabditis elegans by comparative proteomics.
Lai CH, Chou CY, Ch'ang LY, Liu CS, Lin W.
Genome Res 10(5):703-13. 2000