Arginine methylation of MRE11 by PRMT1 is required for DNA damage checkpoint control.
about
MRE11-RAD50-NBS1 is a critical regulator of FANCD2 stability and function during DNA double-strand break repairSIRT1 regulates the function of the Nijmegen breakage syndrome proteinThe transcriptional histone acetyltransferase cofactor TRRAP associates with the MRN repair complex and plays a role in DNA double-strand break repairMethyltransferase PRMT1 is a binding partner of HBx and a negative regulator of hepatitis B virus transcriptionArginine methyltransferases as novel therapeutic targets for breast cancerEnvisioning the dynamics and flexibility of Mre11-Rad50-Nbs1 complex to decipher its roles in DNA replication and repairThe role of protein arginine methylation in the formation of silent chromatinMethylation of Smad6 by protein arginine N-methyltransferase 1Rare key functional domain missense substitutions in MRE11A, RAD50, and NBN contribute to breast cancer susceptibility: results from a Breast Cancer Family Registry case-control mutation-screening studyProtein arginine methylation in mammals: who, what, and whyProteome-wide analysis of arginine monomethylation reveals widespread occurrence in human cellsArginine methylation of yeast mRNA-binding protein Npl3 directly affects its function, nuclear export, and intranuclear protein interactions.Thrombospondin-1 is a transcriptional repression target of PRMT6.Methylation of the tumor suppressor protein, BRCA1, influences its transcriptional cofactor function.Histone arginine methylations: their roles in chromatin dynamics and transcriptional regulation.Methylation of histone H4 by arginine methyltransferase PRMT1 is essential in vivo for many subsequent histone modificationsThe MRE11 GAR motif regulates DNA double-strand break processing and ATR activation.Coilin is rapidly recruited to UVA-induced DNA lesions and γ-radiation affects localized movement of Cajal bodiesMethylation of FEN1 suppresses nearby phosphorylation and facilitates PCNA bindingEmerging technologies to map the protein methylome.Autoregulation of ribosome biosynthesis by a translational response in fission yeast.Fanconi anemia group J helicase and MRE11 nuclease interact to facilitate the DNA damage response.Subcellular proteomics reveals a role for nucleo-cytoplasmic trafficking at the DNA replication origin activation checkpointA role for the arginine methylation of Rad9 in checkpoint control and cellular sensitivity to DNA damage.Protein arginine methylation in parasitic protozoa.The Tudor domain protein Spindlin1 is involved in intrinsic antiviral defense against incoming hepatitis B Virus and herpes simplex virus type 1Protein arginine methyltransferase 7 promotes breast cancer cell invasion through the induction of MMP9 expressionThe HPV E6 oncoprotein targets histone methyltransferases for modulating specific gene transcription.Proteomic responses to elevated ocean temperature in ovaries of the ascidian Ciona intestinalis.Inhibition of methyltransferases results in induction of g2/m checkpoint and programmed cell death in human T-lymphotropic virus type 1-transformed cells.The dual function of PRMT1 in modulating epithelial-mesenchymal transition and cellular senescence in breast cancer cells through regulation of ZEB1Alternatively spliced protein arginine methyltransferase 1 isoform PRMT1v2 promotes the survival and invasiveness of breast cancer cells.Effect of methylation on the side-chain pKa value of arginineProtein arginine methyltransferases: from unicellular eukaryotes to humansSmall Molecule Inhibitors of Protein Arginine Methyltransferases.Novel functions of protein arginine methyltransferase 1 in thyroid hormone receptor-mediated transcription and in the regulation of metamorphic rate in Xenopus laevis.Mre11 nuclease activity has essential roles in DNA repair and genomic stability distinct from ATM activation.Minireview: protein arginine methylation of nonhistone proteins in transcriptional regulationA mouse PRMT1 null allele defines an essential role for arginine methylation in genome maintenance and cell proliferationDisease-associated MRE11 mutants impact ATM/ATR DNA damage signaling by distinct mechanisms.
P2860
Q24315682-E545BDD4-C39B-418B-9492-02D215E85C52Q24317230-9A351156-CC97-48D3-89C8-0B8527E2F10EQ24537586-E4FF785F-02C6-40C7-A3E9-F415CB854DBFQ24634260-2C89C82D-5517-42EE-BF34-1DD6715B8028Q26851594-CC3E5900-E778-43A0-8A8F-2C226BBDB7FFQ28085622-48B13EC4-2CB4-4675-8BC7-6E3E80A3D170Q28278117-138F8373-0739-4365-987B-BDFAF1FDEF78Q28510844-1FC64D05-BC98-4ED0-9A72-5D0BEFD62472Q28652308-90F44D4D-8603-45C1-AFAE-76D325BDF4CEQ29617309-71ABD42C-1F39-4E1B-BF96-5D6FBDFDD7B7Q30002318-522F9B0A-CF04-4D18-88D6-1FA1415E14BAQ30791977-9A82C62B-722E-4AA0-BFE7-367445C94314Q32884548-01575BB7-B842-42DE-9AC2-20CBF16558E9Q33627677-8A18DFD3-AE03-4FC1-813C-3BD817CE31DBQ33694050-7EF8DB9B-42F7-4B71-A5BB-00E22A0DD921Q33917698-691B02B3-033E-4535-B5E3-1B565CD7AA3FQ33985893-E29E89D9-724D-4EF5-9C68-8AED8F61A16AQ34046669-5222B896-0FE6-4460-95D5-131433ABFBB0Q34143246-C44C0784-E9DF-4F31-9993-C588194CC24EQ34254532-D8E683CB-D71C-45F0-BF9F-B5DD7A07E9CDQ34519699-8BB42F40-6753-4567-A291-953B40C4B3BAQ34636203-9B4A54F7-5B6C-42AB-845E-F6BD94ACCB82Q34667732-B6CF59FF-3796-4637-89D4-9EA81D622E82Q35040908-AEE6A8D6-3CD9-4E5C-8755-230AD3B47DD6Q35191784-CB2A88D6-B49C-4731-BCD1-8A02DDE8E59EQ35248001-20FD4980-C5CC-4FE9-A779-11E874453D1EQ35550160-DBD9DD97-D0F8-45E9-A5B7-6FDF0C72C8B3Q35949401-F488F1CE-D304-4E35-8DBA-454144C1AF32Q36370775-2555E5EF-642F-4CE8-B0E5-1C3D375C8FBEQ36424037-C7730192-2DAB-4D8C-938D-CDE8C1F01F6EQ36507087-3A18C188-342B-420A-A385-AB89F73BCB36Q36581678-EC0C938C-339B-4170-BB01-BC5ED296BBE6Q36749523-6B395602-5C3B-4726-B86E-AF7FFB88070AQ36806235-389FDF1F-E6C1-4ABD-8F77-DD941C041057Q37056442-2FE98FBA-5008-4CC7-8090-CDCD87BD0C05Q37072140-97E6431B-AB74-4862-9414-D0F9078525C7Q37104813-D2BE47E0-054D-4622-9D9F-789CB2DB74EEQ37155394-B487918A-1BA5-4759-B732-FA3A2992CCA5Q37191986-F855D75B-A324-4427-A815-27F5C4BB7B2AQ37346970-6ED65993-9B11-4618-9C91-9BC5E626FF44
P2860
Arginine methylation of MRE11 by PRMT1 is required for DNA damage checkpoint control.
description
2005 nî lūn-bûn
@nan
2005 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի մարտին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Arginine methylation of MRE11 by PRMT1 is required for DNA damage checkpoint control.
@ast
Arginine methylation of MRE11 by PRMT1 is required for DNA damage checkpoint control.
@en
type
label
Arginine methylation of MRE11 by PRMT1 is required for DNA damage checkpoint control.
@ast
Arginine methylation of MRE11 by PRMT1 is required for DNA damage checkpoint control.
@en
prefLabel
Arginine methylation of MRE11 by PRMT1 is required for DNA damage checkpoint control.
@ast
Arginine methylation of MRE11 by PRMT1 is required for DNA damage checkpoint control.
@en
P2093
P2860
P356
P1433
P1476
Arginine methylation of MRE11 by PRMT1 is required for DNA damage checkpoint control
@en
P2093
Jean-Yves Masson
Stéphane Richard
P2860
P304
P356
10.1101/GAD.1279805
P577
2005-03-01T00:00:00Z