Literature for peptidase M41.026: YME1L1 g.p. (Homo sapiens) and similar
(Topics flags: M Mutation, K Knockout. To select only the references relevant to a single topic, click the link above. See explanation.)
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Demetriadou,A., Grafakou,O., Georgiou,T., Burska,D., Malekkou,A., Krizova,J., Paramera,E., Mavrikiou,G., Dionysiou,M., Theodosiou,A., Sismani,C., Anastasiadou,V., Ioannou,I., Papakonstantinou,E., Hansikova,H., Drousiotou,A. and Petrou,P.P.
YME1L1 Dysfunction Associated With 3-Methylglutaconic Aciduria
J Inherit Metab Dis48, e70029-e70029. PubMed Europe PubMed DOI -
Eldeeb,M.A., Shahid,M. and Fon,E.A.
Cell biology: Mitochondrial protease degrades unoccupied translocases upon import stress
Curr Biol35, R287-R287. PubMed Europe PubMed DOI -
Hsu,M.C., Kinefuchi,H., Lei,L., Kikuchi,R., Yamano,K. and Youle,R.J.
Mitochondrial YME1L1 governs unoccupied protein translocase channels
Nat Cell Biol PubMed Europe PubMed DOI -
Baker,M.J., Blau,K.U., Anderson,A.J., Palmer,C.S., Fielden,L.F., Crameri,J.J., Milenkovic,D., Thorburn,D.R., Frazier,A.E., Langer,T. and Stojanovski,D.
CLPB disaggregase dysfunction impacts the functional integrity of the proteolytic SPY complex
J Cell Biol223, PubMed Europe PubMed DOI -
Tan,S., Dengler,A.S., Darawsheh,R.Z. and Kory,N.
The iAAA-mitochondrial protease YME1L1 regulates the degradation of the short-lived mitochondrial transporter SLC25A38
bioRxiv PubMed Europe PubMed DOI -
Xin,W., Zhou,J., Peng,Y., Gong,S., Liao,W., Wang,Y., Huang,X., Mao,Y., Yao,M., Qin,S., Xiong,J., Li,Y., Lan,Q., Huang,Y. and Zhao,J.
SREBP1c-Mediated Transcriptional Repression of YME1L1 Contributes to Acute Kidney Injury by Inducing Mitochondrial Dysfunction in Tubular Epithelial Cells
Adv Sci (Weinh)e2412233-e2412233. PubMed Europe PubMed DOI -
Qiu,J., Yue,F., Zhu,P., Chen,J., Xu,F., Zhang,L., Kim,K.H., Snyder,M.M., Luo,N., Xu,H.W., Huang,F., Tao,W.A. and Kuang,S.
FAM210A is essential for cold-induced mitochondrial remodeling in brown adipocytes
Nat Commun14, 6344-6344. PubMed Europe PubMed DOI -
Zhou,D., Sun,M.H., Jiang,W.J., Li,X.H., Lee,S.H., Heo,G., Choi,J., Kim,K.S. and Cui,X.S.
Knock-down of YME1L1 induces mitochondrial dysfunction during early porcine embryonic development
Front Cell Dev Biol11, 1147095-1147095. PubMed Europe PubMed DOI K -
Purandare,N., Kunji,Y., Xi,Y., Romero,R., Gomez-Lopez,N., Fribley,A., Grossman,L.I. and Aras,S.
Lipopolysaccharide induces placental mitochondrial dysfunction in murine and human systems by reducing MNRR1 levels via a TLR4-independent pathway
iScience25, 105342-105342. PubMed Europe PubMed DOI -
Sprenger,H.G., MacVicar,T., Bahat,A., Fiedler,K.U., Hermans,S., Ehrentraut,D., Ried,K., Milenkovic,D., Bonekamp,N., Larsson,N.G., Nolte,H., Giavalisco,P. and Langer,T.
Cellular pyrimidine imbalance triggers mitochondrial DNA-dependent innate immunity
Nat Metab3, 636-650. PubMed Europe PubMed DOI -
Lee,Y.J., Kim,G.H., Park,S.I. and Lim,J.H.
Down-regulation of the mitochondrial i-AAA protease Yme1L induces muscle atrophy via FoxO3a and myostatin activation
J Cell Mol Med24, 899-909. PubMed Europe PubMed DOI K -
Li,S., Wu,Z., Tantray,I., Li,Y., Chen,S., Dong,J., Glynn,S., Vogel,H., Snyder,M. and Lu,B.
Quality-control mechanisms targeting translationally stalled and C-terminally extended poly(GR) associated with ALS/FTD
Proc Natl Acad Sci U S A117, 25104-25115. PubMed Europe PubMed DOI -
Miller,J.M., Brambley,C.A. and Marsee,J.D.
Examination of the Role of Mg(2+) in the Mechanism of Nucleotide Binding to the Monomeric YME1L AAA+ Domain
Biochemistry59, 4303-4320. PubMed Europe PubMed DOI -
Moore,S., Pickens,A., Rodriguez,J.L., Marsee,J.D. and Miller,J.M.
Fluorescence methods applied to the description of urea-dependent YME1L protease unfolding
Biomolecules10, 656-656. PubMed Europe PubMed DOI -
Ohba,Y., MacVicar,T. and Langer,T.
Regulation of mitochondrial plasticity by the i-AAA protease YME1L
Biol Chem401, 877-890. PubMed Europe PubMed DOI -
Ando,K., Yokochi,T., Mukai,A., Wei,G., Li,Y., Kramer,S., Ozaki,T., Maehara,Y. and Nakagawara,A.
Tumor suppressor KIF1Bbeta regulates mitochondrial apoptosis in collaboration with YME1L1
Mol Carcinog58, 1134-1144. PubMed Europe PubMed DOI -
Brambley,C.A., Marsee,J.D., Halper,N. and Miller,J.M.
Characterization of mitochondrial YME1L protease oxidative stress-induced conformational state
J Mol Biol431, 1250-1266. PubMed Europe PubMed DOI -
MacVicar,T., Ohba,Y., Nolte,H., Mayer,F.C., Tatsuta,T., Sprenger,H.G., Lindner,B., Zhao,Y., Li,J., Bruns,C., Kruger,M., Habich,M., Riemer,J., Schwarzer,R., Pasparakis,M., Henschke,S., Bruning,J.C., Zamboni,N. and Langer,T.
Lipid signalling drives proteolytic rewiring of mitochondria by YME1L
Nature575, 361-365. PubMed Europe PubMed DOI -
Richter,F., Dennerlein,S., Nikolov,M., Jans,D.C., Naumenko,N., Aich,A., MacVicar,T., Linden,A., Jakobs,S., Urlaub,H., Langer,T. and Rehling,P.
ROMO1 is a constituent of the human presequence translocase required for YME1L protease import
J Cell Biol218, 598-614. PubMed Europe PubMed DOI -
Cesnekova,J., Rodinova,M., Hansikova,H., Zeman,J. and Stiburek,L.
Loss of mitochondrial AAA proteases AFG3L2 and YME1L impairs mitochondrial structure and respiratory chain biogenesis
Int J Mol Sci19, 3930-3930. PubMed Europe PubMed DOI K -
Sprenger,H.G., Wani,G., Hesseling,A., Konig,T., Patron,M., MacVicar,T., Ahola,S., Wai,T., Barth,E., Rugarli,E.I., Bergami,M. and Langer,T.
Loss of the mitochondrial i-AAA protease YME1L leads to ocular dysfunction and spinal axonopathy
EMBO Mol Med11, e9288-e9288. PubMed Europe PubMed DOI M -
Srinivasainagendra,V., Sandel,M.W., Singh,B., Sundaresan,A., Mooga,V.P., Bajpai,P., Tiwari,H.K. and Singh,K.K.
Migration of mitochondrial DNA in the nuclear genome of colorectal adenocarcinoma
Genome Med9, 31-31. PubMed Europe PubMed DOI M -
[YEAR:15-3-2016]Cesnekova,J., Rodinova,M., Hansikova,H., Houstek,J., Zeman,J. and Stiburek,L.
The mammalian homologue of yeast Afg1 ATPase (lactation elevated 1) mediates degradation of nuclear-encoded complex IV subunits
Biochem J473, 797-804. PubMed Europe PubMed -
Hartmann,B., Wai,T., Hu,H., MacVicar,T., Musante,L., Fischer-Zirnsak,B., Stenzel,W., Graf,R., van den Heuvel,L., Ropers,H.H., Wienker,T.F., Hubner,C., Langer,T. and Kaindl,A.M.
Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentation
elife5, e16078-e16078. PubMed Europe PubMed DOI M -
MacVicar,T. and Langer,T.
OPA1 processing in cell death and disease - the long and short of it
J Cell Sci129, 2297-2306. PubMed Europe PubMed DOI -
Rainbolt,T.K., Saunders,J.M. and Wiseman,R.L.
YME1L degradation reduces mitochondrial proteolytic capacity during oxidative stress
EMBO Rep16, 97-106. PubMed Europe PubMed DOI -
Shi,H., Rampello,A.J. and Glynn,S.E.
Engineered AAA+ proteases reveal principles of proteolysis at the mitochondrial inner membrane
Nat Commun7, 13301-13301. PubMed Europe PubMed DOI -
Anand,R., Wai,T., Baker,M.J., Kladt,N., Schauss,A.C., Rugarli,E. and Langer,T.
The i-AAA protease YME1L and OMA1 cleave OPA1 to balance mitochondrial fusion and fission
J Cell Biol204, 919-929. PubMed Europe PubMed DOI -
Ruan,Y., Li,H., Zhang,K., Jian,F., Tang,J. and Song,Z.
Loss of Yme1L perturbates mitochondrial dynamics
Cell Death Dis4, e896-e896. PubMed Europe PubMed DOI -
Stiburek,L., Cesnekova,J., Kostkova,O., Fornuskova,D., Vinsova,K., Wenchich,L., Houstek,J. and Zeman,J.
YME1L controls the accumulation of respiratory chain subunits and is required for apoptotic resistance, cristae morphogenesis, and cell proliferation
Mol Biol Cell23, 1010-1023. PubMed Europe PubMed DOI -
Head,B., Griparic,L., Amiri,M., Gandre-Babbe,S. and van der Bliek,A.M.
Inducible proteolytic inactivation of OPA1 mediated by the OMA1 protease in mammalian cells
J Cell Biol187, 959-966. PubMed Europe PubMed DOI -
Song,Z., Chen,H., Fiket,M., Alexander,C. and Chan,D.C.
OPA1 processing controls mitochondrial fusion and is regulated by mRNA splicing, membrane potential, and Yme1L
J Cell Biol178, 749-755. PubMed Europe PubMed DOI -
Coenen,M.J., Smeitink,J.A., Smeets,R., Trijbels,F.J. and van den Heuvel,L.P.
Mutation detection in four candidate genes (OXA1L, MRS2L, YME1L and MIPEP) for combined deficiencies in the oxidative phosphorylation system
J Inherit Metab Dis28, 1091-1097. PubMed Europe PubMed DOI M -
[YEAR:15-5-2000]Coppola,M., Pizzigoni,A., Banfi,S., Bassi,M.T., Casari,G. and Incerti,B.
Identification and characterization of YME1L1, a novel paraplegin-related gene
Genomics66, 48-54. PubMed Europe PubMed DOI -
[YEAR:4-8-2000]Shah,Z.H., Hakkaart,G.A., Arku,B., de Jong,L., van der Spek,H., Grivell,L.A. and Jacobs,H.T.
The human homologue of the yeast mitochondrial AAA metalloprotease Yme1p complements a yeast yme1 disruptant
FEBS Lett478, 267-270. PubMed Europe PubMed DOI
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