-
Články
- Časopisy
- Kurzy
- Témy
- Kongresy
- Videa
- Podcasty
Mck1 kinase is a new player in the DNA damage checkpoint pathway
Autoři: Nerea Sanvisens Delgado aff001; David P. Toczyski aff001
Působiště autorů: UCSF Helen Diller Comprehensive Cancer Center, Univerisity of Califorinia, San Francisco, California, United States of America aff001
Vyšlo v časopise: Mck1 kinase is a new player in the DNA damage checkpoint pathway. PLoS Genet 15(10): e32767. doi:10.1371/journal.pgen.1008372
Kategorie: Perspective
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1008372
Zdroje
1. Ciccia A, Elledge SJ. The DNA Damage Response: Making It Safe to Play with Knives. Molecular Cell. 2010; doi: 10.1016/j.molcel.2010.09.019 20965415
2. Chen SH, Smolka MB, Zhou H. Mechanism of Dun1 activation by Rad53 phosphorylation in Saccharomyces cerevisiae. J Biol Chem. 2007; doi: 10.1074/jbc.M609322200 17114794
3. Rogakou EP, Pilch DR, Orr AH, Ivanova VS, Bonner WM. DNA double-stranded breaks induce histone H2AX phosphorylation on serine 139. J Biol Chem. 1998; doi: 10.1074/jbc.273.10.5858 9488723
4. Ward IM, Chen J. Histone H2AX Is Phosphorylated in an ATR-dependent Manner in Response to Replicational Stress. J Biol Chem. 2001; doi: 10.1074/jbc.C100569200 11673449
5. Ohouo PY, Bastos de Oliveira FM, Almeida BS, Smolka MB. DNA damage signaling recruits the Rtt107-Slx4 scaffolds via Dpb11 to Mediate replication stress response. Mol Cell. 2010; doi: 10.1016/j.molcel.2010.06.019 20670896
6. Cussiol JR, Dibitetto D, Pellicioli A, Smolka MB. Slx4 scaffolding in homologous recombination and checkpoint control: lessons from yeast. Chromosoma. 2017; doi: 10.1007/s00412-016-0600-y 27165041
7. Dibitetto D, Ferrari M, Rawal CC, Balint A, Kim T, Zhang Z et al. Slx4 and Rtt107 control checkpoint signalling and DNA resection at double-strand breaks. Nucleic Acids Res. 2016; doi: 10.1093/nar/gkv1080 26490958
8. Lopez-Mosqueda J, Maas NL, Jonsson ZO, Defazio-Eli LG, Wohlschlegel J, Toczyski DP. Damage-induced phosphorylation of Sld3 is important to block late origin firing. Nature. 2010; doi: 10.1038/nature09377 20865002
9. Zegerman P, Diffley JFX. Checkpoint-dependent inhibition of DNA replication initiation by Sld3 and Dbf4 phosphorylation. Nature. 2010; doi: 10.1038/nature09373 20835227
10. Sanchez Y, Bachant J, Wang H, Hu F, Liu D, Tetzlaff M et al. Control of the DNA damage checkpoint by Chk1 and Rad53 protein kinases through distinct mechanisms. Science. 1999; doi: 10.1126/science.286.5442.1166 10550056
11. Zhou Z, Elledge SJ. DUN1 encodes a protein kinase that controls the DNA damage response in yeast. Cell. 1993; doi: 10.1016/0092-8674(93)90321-G
12. Li Xiaoli, Jin Xuejiao, Sharma Sushma, Liu Xiaojing, Zhang Jiaxin, Niu Yanling et al. Mck1 defines a key S-phase checkpoint effector in response to various degrees of replication threats. PLoS Genet. 2019. doi: 10.1371/journal.pgen.1008136 31381575
13. Lee YD, Elledge SJ. Control of ribonucleotide reductase localization through an anchoring mechanism involving Wtm1. Genes Dev. 2006; doi: 10.1101/gad.1380506 16452505
14. Huang M, Zhou Z, Elledge SJ. The DNA replication and damage checkpoint pathways induce transcription by inhibition of the Crt1 repressor. Cell. 1998; doi: 10.1016/S0092-8674(00)81601-3
15. Tsaponina O, Barsoum E, Åström SU, Chabes A. Ixr1 is required for the expression of the ribonucleotide reductase Rnr1 and maintenance of dNTP pools. PLoS Genet. 2011; doi: 10.1371/journal.pgen.1002061 21573136
16. Chabes A, Domkin V, Thelander L. Yeast Sml1, a protein inhibitor of ribonucleotide reductase. J Biol Chem. 1999; doi: 10.1074/jbc.274.51.36679 10593972
17. Zhao X, Muller EGD, Rothstein R. A suppressor of two essential checkpoint genes identifies a novel protein that negatively affects dNTP pools. Mol Cell. 1998; doi: 10.1016/S1097-2765(00)80277-4
18. Zhao X, Chabes A, Domkin V, Thelander L, Rothstein R. The ribonucleotide reductase inhibitor Sml1 is a new target of the Mec1/Rad53 kinase cascade during growth and in response to DNA damage. EMBO J. 2001; doi: 10.1093/emboj/20.13.3544 11432841
19. Yao R, Zhang Z, An X, Bucci B, Perlstein DL, Stubbe J, et al. Subcellular localization of yeast ribonucleotide reductase regulated by the DNA replication and damage checkpoint pathways. Proc Natl Acad Sci. 2003; doi: 10.1073/pnas.1131932100 12732713
20. Lee YD, Wang J, Stubbe JA, Elledge SJ. Dif1 Is a DNA-Damage-Regulated Facilitator of Nuclear Import for Ribonucleotide Reductase. Mol Cell. 2008; doi: 10.1016/j.molcel.2008.08.018 18851834
21. Wu X, Huang M. Dif1 Controls Subcellular Localization of Ribonucleotide Reductase by Mediating Nuclear Import of the R2 Subunit. Mol Cell Biol. 2008; doi: 10.1128/mcb.01388-08 18838542
22. Meurisse J, Bacquin A, Richet N, Charbonnier JB, Ochsenbein F, Peyroche A. Hug1 is an intrinsically disordered protein that inhibits ribonucleotide reductase activity by directly binding Rnr2 subunit. Nucleic Acids Res. 2014; doi: 10.1093/nar/gku1095 25378334
23. Searle JS, Wood MD, Kaur M, Tobin D V., Sanchez Y. Proteins in the Nutrient-Sensing and DNA damage checkpoint pathways cooperate to restrain mitotic progression following DNA damage. PLoS Genet. 2011; doi: 10.1371/journal.pgen.1002176 21779180
24. Edenberg ER, Vashisht AA, Topacio BR, Wohlschlegel JA, Toczyski DP. Hst3 is turned over by a replication stress-responsive SCFCdc4 phospho-degron. Proc Natl Acad Sci. 2014; doi: 10.1073/pnas.1315325111 24715726
25. Al-Zain A, Schroeder L, Sheglov A, Ikui AE. Cdc6 degradation requires phosphodegron created by GSK-3 and Cdk1 for SCF Cdc4 recognition in Saccharomyces cerevisiae. Mol Biol Cell. 2015; doi: 10.1091/mbc.e14-07-1213 25995377
26. Toczyski DP, Galgoczy DJ, Hartwell LH. CDC5 and CKII control adaptation to the yeast DNA damage checkpoint. Cell. 1997; doi: 10.1016/S0092-8674(00)80375-X
27. Bonilla CY, Melo JA, Toczyski DP. Colocalization of Sensors Is Sufficient to Activate the DNA Damage Checkpoint in the Absence of Damage. Mol Cell. 2008; doi: 10.1016/j.molcel.2008.03.023 18471973
28. Bensimon A, Aebersold R, Shiloh Y. Beyond ATM: The protein kinase landscape of the DNA damage response. FEBS Letters. 2011; doi: 10.1016/j.febslet.2011.05.013 21570395
29. Greer YE, Gao B, Yang Y, Nussenzweig A, Rubin JS. Lack of casein kinase 1 delta promotes genomic instability—The accumulation of DNA damage and down-regulation of checkpoint kinase 1. PLoS ONE. 2017; doi: 10.1371/journal.pone.0170903 28125685
30. Gregory MA, Qi Y, Hann SR. Phosphorylation by Glycogen Synthase Kinase-3 Controls c-Myc Proteolysis and Subnuclear Localization. J Biol Chem. 2003; doi: 10.1074/jbc.M310722200 14563837
31. Welcker M, Orian A, Jin J, Grim JA, Harper JW, Eisenman RN, et al. The Fbw7 tumor suppressor regulates glycogen synthase kinase 3 phosphorylation-dependent c-Myc protein degradation. Proc Natl Acad Sci. 2004; doi: 10.1073/pnas.0402770101 15150404
32. Reinhardt HC, Yaffe MB. Kinases that control the cell cycle in response to DNA damage: Chk1, Chk2, and MK2. Current Opinion in Cell Biology. 2009; doi: 10.1016/j.ceb.2009.01.018 19230643
33. Picco V, Pagès G. Linking JNK Activity to the DNA Damage Response. Genes and Cancer. 2013; doi: 10.1177/1947601913486347 24349633
34. Wu ZH, Shi Y, Tibbetts RS, Miyamoto S. Molecular linkage between the kinase ATM and NF-κB signaling in response to genotoxic stimuli. Science. 2006; doi: 10.1126/science.1121513 16497931
35. Bulavin D V., Higashimoto Y, Popoff IJ, Gaarde WA, Basrur V, Potapova O.Initiation of a G2/M checkpoint after ultraviolet radiation requires p38 kinase. Nature. 2001; doi: 10.1038/35075107 11333986
36. Guo Z, Kozlov S, Lavin MF, Person MD, Paull TT. ATM activation by oxidative stress. Science. 2010; doi: 10.1126/science.1192912 20966255
37. Paull TT. Mechanisms of ATM Activation. Annu Rev Biochem. 2015; doi: 10.1146/annurev-biochem-060614-034335 25580527
38. Hilioti Z, Gallagher DA, Low-Nam ST, Ramaswamy P, Gajer P, Kingsbury TJ. GSK-3 kinases enhance calcineurin signaling by phosphorylation of RCNs. Genes Dev. 2004; doi: 10.1101/gad.1159204 14701880
39. Brazill DT, Thorner J, Martin GS. Mck1, a member of the glycogen synthase kinase 3 family of protein kinases, is a negative regulator of pyruvate kinase in the yeast Saccharomyces cerevisiae. J Bacteriol. 1997; doi: 10.1128/jb.179.13.4415–4418.1997
40. Griffioen G, Swinnen S, Thevelein JM. Feedback inhibition on cell wall integrity signaling by Zds1 involves Gsk3 phosphorylation of a cAMP-dependent protein kinase regulatory subunit. J Biol Chem. 2003; doi: 10.1074/jbc.M210691200 12704202
41. Neigeborn L, Mitchell AP. The yeast MCK1 gene encodes a protein kinase homolog that activates early meiotic gene expression. Genes Dev. 1991; doi: 10.1101/gad.5.4.533 2010083
42. Schwartz MA, Madhani HD. Principles of MAP Kinase Signaling Specificity in Saccharomyces cerevisiae. Annu Rev Genet. 2004; doi: 10.1146/annurev.genet.39.073003.112634 15568991
Štítky
Genetika Reprodukčná medicína
Článek Viral quasispeciesČlánek Differential Requirements for the RAD51 Paralogs in Genome Repair and Maintenance in Human CellsČlánek Genetic mapping of fitness determinants across the malaria parasite Plasmodium falciparum life cycle
Článok vyšiel v časopisePLOS Genetics
Najčítanejšie tento týždeň
2019 Číslo 10- Gynekologové a odborníci na reprodukční medicínu se sejdou na prvním virtuálním summitu
- Je „freeze-all“ pro všechny? Odborníci na fertilitu diskutovali na virtuálním summitu
-
Všetky články tohto čísla
- HRPK-1, a conserved KH-domain protein, modulates microRNA activity during Caenorhabditis elegans development
- Dysregulation of STAT3 signaling is associated with endplate-oriented herniations of the intervertebral disc in Adgrg6 mutant mice
- Local adaptation drives the diversification of effectors in the fungal wheat pathogen Parastagonospora nodorum in the United States
- Biofilm-associated toxin and extracellular protease cooperatively suppress competitors in Bacillus subtilis biofilms
- Mutations of the Bacillus subtilis YidC1 (SpoIIIJ) insertase alleviate stress associated with σM-dependent membrane protein overproduction
- Viral quasispecies
- A functional regulatory variant of MYH3 influences muscle fiber-type composition and intramuscular fat content in pigs
- INX-18 and INX-19 play distinct roles in electrical synapses that modulate aversive behavior in Caenorhabditis elegans
- MR-pheWAS with stratification and interaction: Searching for the causal effects of smoking heaviness identified an effect on facial aging
- Tnni3k alleles influence ventricular mononuclear diploid cardiomyocyte frequency
- Differential Requirements for the RAD51 Paralogs in Genome Repair and Maintenance in Human Cells
- Ataxin2 functions via CrebA to mediate Huntingtin toxicity in circadian clock neurons
- Genetic factors define CPO and CLO subtypes of nonsyndromicorofacial cleft
- The quorum sensing transcription factor AphA directly regulates natural competence in Vibrio cholerae
- Mck1 kinase is a new player in the DNA damage checkpoint pathway
- A small set of conserved genes, including sp5 and Hox, are activated by Wnt signaling in the posterior of planarians and acoels
- Causal relationships between obesity and the leading causes of death in women and men
- Macrophages fine tune satellite cell fate in dystrophic skeletal muscle of mdx mice
- Optimizing clinical exome design and parallel gene-testing for recessive genetic conditions in preconception carrier screening: Translational research genomic data from 14,125 exomes
- Manipulating mtDNA in vivo reprograms metabolism via novel response mechanisms
- TSEN54 missense variant in Standard Schnauzers with leukodystrophy
- Centromeric SMC1 promotes centromer clustering and stabilizes meiotic homolog pairing
- A RAPGEF6 variant constitutes a major risk factor for laryngeal paralysis in dogs
- GPCR-mediated glucose sensing system regulates light-dependent fungal development and mycotoxin production
- Kinetochore-associated Stu2 promotes chromosome biorientation in vivo
- Metabolic effects of skeletal muscle-specific deletion of beta-arrestin-1 and -2 in mice
- NusG prevents transcriptional invasion of H-NS-silenced genes
- The effects of manipulating levels of replication initiation factors on origin firing efficiency in yeast
- Bayesian multivariate reanalysis of large genetic studies identifies many new associations
- Bacillus subtilis PgcA moonlights as a phosphoglucosamine mutase in support of peptidoglycan synthesis
- Protease-associated import systems are widespread in Gram-negative bacteria
- Expression of Concern: Exome sequencing in multiple sclerosis families identifies 12 candidate genes and nominates biological pathways for the genesis of disease
- Evaluating the strength of genetic results: Risks and responsibilities
- Spatiotemporal cytoskeleton organizations determine morphogenesis of multicellular trichomes in tomato
- Loss of thymidine kinase 1 inhibits lung cancer growth and metastatic attributes by reducing GDF15 expression
- Histone deposition promotes recombination-dependent replication at arrested forks
- Synergistic action of the transcription factors Krüppel homolog 1 and Hairy in juvenile hormone/Methoprene-tolerant-mediated gene-repression in the mosquito Aedes aegypti
- Low affinity binding sites in an activating CRM mediate negative autoregulation of the Drosophila Hox gene Ultrabithorax
- A novel system of bacterial cell division arrest implicated in horizontal transmission of an integrative and conjugative element
- PilT and PilU are homohexameric ATPases that coordinate to retract type IVa pili
- The comprehensive role of E-cadherin in maintaining prostatic epithelial integrity during oncogenic transformation and tumor progression
- Genetic mapping of fitness determinants across the malaria parasite Plasmodium falciparum life cycle
- A missense mutation in SNRPE linked to non-syndromal microcephaly interferes with U snRNP assembly and pre-mRNA splicing
- CRISPR editing of sftb-1/SF3B1 in Caenorhabditis elegans allows the identification of synthetic interactions with cancer-related mutations and the chemical inhibition of splicing
- Nitrate-responsive OBP4-XTH9 regulatory module controls lateral root development in Arabidopsis thaliana
- Paralog buffering contributes to the variable essentiality of genes in cancer cell lines
- Splice variants of DOMINO control Drosophila circadian behavior and pacemaker neuron maintenance
- Duplicate divergence of two bacterial small heat shock proteins reduces the demand for Hsp70 in refolding of substrates
- PLOS Genetics
- Archív čísel
- Aktuálne číslo
- Informácie o časopise
Najčítanejšie v tomto čísle- Spatiotemporal cytoskeleton organizations determine morphogenesis of multicellular trichomes in tomato
- Loss of thymidine kinase 1 inhibits lung cancer growth and metastatic attributes by reducing GDF15 expression
- Synergistic action of the transcription factors Krüppel homolog 1 and Hairy in juvenile hormone/Methoprene-tolerant-mediated gene-repression in the mosquito Aedes aegypti
- TSEN54 missense variant in Standard Schnauzers with leukodystrophy
Prihlásenie#ADS_BOTTOM_SCRIPTS#Zabudnuté hesloZadajte e-mailovú adresu, s ktorou ste vytvárali účet. Budú Vám na ňu zasielané informácie k nastaveniu nového hesla.
- Časopisy