Littérature scientifique sur le sujet « RecQ4 helicases »
Créez une référence correcte selon les styles APA, MLA, Chicago, Harvard et plusieurs autres
Consultez les listes thématiques d’articles de revues, de livres, de thèses, de rapports de conférences et d’autres sources académiques sur le sujet « RecQ4 helicases ».
À côté de chaque source dans la liste de références il y a un bouton « Ajouter à la bibliographie ». Cliquez sur ce bouton, et nous générerons automatiquement la référence bibliographique pour la source choisie selon votre style de citation préféré : APA, MLA, Harvard, Vancouver, Chicago, etc.
Vous pouvez aussi télécharger le texte intégral de la publication scolaire au format pdf et consulter son résumé en ligne lorsque ces informations sont inclues dans les métadonnées.
Articles de revues sur le sujet "RecQ4 helicases"
Thangavel, Saravanabhavan, Ramiro Mendoza-Maldonado, Erika Tissino, Julia M. Sidorova, Jinhu Yin, Weidong Wang, Raymond J. Monnat, Arturo Falaschi et Alessandro Vindigni. « Human RECQ1 and RECQ4 Helicases Play Distinct Roles in DNA Replication Initiation ». Molecular and Cellular Biology 30, no 6 (11 janvier 2010) : 1382–96. http://dx.doi.org/10.1128/mcb.01290-09.
Texte intégralBACHRATI, Csanád Z., et Ian D. HICKSON. « RecQ helicases : suppressors of tumorigenesis and premature aging ». Biochemical Journal 374, no 3 (15 septembre 2003) : 577–606. http://dx.doi.org/10.1042/bj20030491.
Texte intégralRogers, Cody M., Elsbeth Sanders, Phoebe A. Nguyen, Whitney Smith-Kinnaman, Amber L. Mosley et Matthew L. Bochman. « The Genetic and Physical Interactomes of the Saccharomyces cerevisiae Hrq1 Helicase ». G3: ; Genes|Genomes|Genetics 10, no 12 (28 octobre 2020) : 4347–57. http://dx.doi.org/10.1534/g3.120.401864.
Texte intégralRogers, Cody M., Chun-Ying Lee, Samuel Parkins, Nicholas J. Buehler, Sabine Wenzel, Francisco Martínez-Márquez, Yuichiro Takagi, Sua Myong et Matthew L. Bochman. « The yeast Hrq1 helicase stimulates Pso2 translesion nuclease activity and thereby promotes DNA interstrand crosslink repair ». Journal of Biological Chemistry 295, no 27 (5 mai 2020) : 8945–57. http://dx.doi.org/10.1074/jbc.ra120.013626.
Texte intégralSéguéla-Arnaud, Mathilde, Wayne Crismani, Cécile Larchevêque, Julien Mazel, Nicole Froger, Sandrine Choinard, Afef Lemhemdi et al. « Multiple mechanisms limit meiotic crossovers : TOP3α and two BLM homologs antagonize crossovers in parallel to FANCM ». Proceedings of the National Academy of Sciences 112, no 15 (30 mars 2015) : 4713–18. http://dx.doi.org/10.1073/pnas.1423107112.
Texte intégralPark, Youngji, Guangbin Luo et Stanton Gerson. « Repopulation Advantage of Blm−/− Cells in the Primary Recipients Can Be Reversed by Cisplatin Treatment. » Blood 104, no 11 (16 novembre 2004) : 2683. http://dx.doi.org/10.1182/blood.v104.11.2683.2683.
Texte intégralCheok, C. F., C. Z. Bachrati, K. L. Chan, C. Ralf, L. Wu et I. D. Hickson. « Roles of the Bloom's syndrome helicase in the maintenance of genome stability ». Biochemical Society Transactions 33, no 6 (26 octobre 2005) : 1456–59. http://dx.doi.org/10.1042/bst0331456.
Texte intégralGarige, Mamatha, et Sudha Sharma. « Cellular Deficiency of Werner Syndrome Protein or RECQ1 Promotes Genotoxic Potential of Hydroquinone and Benzo[a]pyrene Exposure ». International Journal of Toxicology 33, no 5 (septembre 2014) : 373–81. http://dx.doi.org/10.1177/1091581814547422.
Texte intégralGupta, Sonia Vidushi, et Kristina Hildegard Schmidt. « Maintenance of Yeast Genome Integrity by RecQ Family DNA Helicases ». Genes 11, no 2 (18 février 2020) : 205. http://dx.doi.org/10.3390/genes11020205.
Texte intégralPike, Ashley C. W., Shivasankari Gomathinayagam, Paolo Swuec, Matteo Berti, Ying Zhang, Christina Schnecke, Francesca Marino et al. « Human RECQ1 helicase-driven DNA unwinding, annealing, and branch migration : Insights from DNA complex structures ». Proceedings of the National Academy of Sciences 112, no 14 (23 mars 2015) : 4286–91. http://dx.doi.org/10.1073/pnas.1417594112.
Texte intégralThèses sur le sujet "RecQ4 helicases"
THANGAVEL, SARAVANA BHAVAN. « Characterization of the Role of RecQ helicases in human DNA replication ». Doctoral thesis, Scuola Normale Superiore, 2010. http://hdl.handle.net/11384/85963.
Texte intégralMojumdar, Aditya. « Structural and Biochemical study of human RECQ4 ». Doctoral thesis, Università degli studi di Trieste, 2015. http://hdl.handle.net/10077/11141.
Texte intégralRecQ helicases belong to a ubiquitous family of DNA unwinding enzymes that are essential to maintain genome stability by acting at the interface between DNA replication, recombination and repair. Humans have five different paralogues of RecQ helicases namely RecQ1, BLM, WRN, RecQ4 and RecQ5. This work focuses on the structural and biochemical study of human RecQ4. Germ-line mutations in the RECQ4 gene give rise to three distinct human genetic disorders (Rothmund-Thomson, RAPADILINO and Baller-Gerold syndromes). Despite the important roles of RecQ4 in various cellular processes, RecQ4 have never been fully characterized. In addition to the helicase domain, RecQ4 has a unique N-terminal part that is essential for viability and is constituted by a region homologous to the yeast Sld2 replication initiation factor, followed by a cysteine-rich region, predicted to fold as a Zn knuckle. A part of this work focuses on the structural and biochemical analysis of both the human and Xenopus RecQ4 cysteine-rich regions, and shows by NMR spectroscopy that the Xenopus fragment does indeed assumes the canonical Zn knuckle fold, whereas the human sequence remains unstructured, consistent with the mutation of one of the Zn ligands. Both the human and Xenopus Zn knuckles bind to a variety of nucleic acid substrates, with a preference for RNA. We also investigated the effect of an additional Sld2 homologous region upstream the Zn knuckle. In both the human and Xenopus system, the presence of this region strongly enhances binding to nucleic acids. These results reveal novel possible roles of RecQ4 in DNA replication and genome stability. Recently the catalytic core of RecQ4 has been predicted to include RecQ-like-C-terminal (RQC) domain at the C-terminus of the helicase domain, similar to other RecQ helicases. This domain is composed of a Zn-binding region and a winged helix (WH) domain. Another part of this thesis centers on the structural and biochemical characterization of the catalytic core of RecQ4 including the helicase and RQC domain. The results provide an insight in the Zn binding ligands present in the RQC domain that plays a role in DNA binding and unwinding activity of the protein. Also the presence of the characteristic aromatic residue at the tip of the WH β hairpin and its role in DNA binding and unwinding has been established. Finally, it provides a low resolution SAXS model of the catalytic core of RecQ4.
Elicasi RecQ appartengono a una famiglia ubiquitaria di DNA svolgimento enzimi che sono essenziali per mantenere la stabilità del genoma agendo all'interfaccia tra replicazione del DNA, ricombinazione e riparazione. Gli esseri umani hanno cinque diversi paralogues di RecQ elicasi cioè RecQ1, BLM, WRN, RecQ4 e RecQ5. Questo lavoro si concentra sullo studio strutturale e biochimica di RecQ4 umana. Mutazioni germinali nel gene RECQ4 danno luogo a tre malattie genetiche umane distinte (Rothmund-Thomson, RAPADILINO e sindromi Baller-Gerold). Nonostante i ruoli importanti di RecQ4 in diversi processi cellulari, RecQ4 non sono mai stati pienamente caratterizzato. In aggiunta al dominio elicasi, RecQ4 ha una parte unica N-terminale che è essenziale per la vitalità ed è costituito da una regione omologa al lievito Sld2 fattore di iniziazione replica, seguita da una regione ricca di cisteina, previsto per piegare come stinco Zn . Una parte di questo lavoro si concentra sull'analisi strutturale e biochimica sia della regioni ricche di cisteina Xenopus RecQ4 umana e, e spettacoli di spettroscopia NMR che il frammento Xenopus effettivamente assume la canonica Zn nocca volte, mentre la sequenza di resti umani non strutturato, coerente con la mutazione di uno dei ligandi Zn. Sia il nocche Xenopus Zn umana e si legano ad una varietà di substrati di acido nucleico, con una preferenza per l'RNA. Abbiamo anche studiato l'effetto di un ulteriore regione omologa Sld2 monte la nocca Zn. Sia il sistema Xenopus umano e, la presenza di questa regione migliora fortemente legame ad acidi nucleici. Questi risultati rivelano possibili ruoli nuovi di RecQ4 nella replicazione del DNA e la stabilità del genoma. Recentemente il nucleo catalitico di RecQ4 stato previsto per includere RecQ-like-C-terminale (RQC) dominio al C-terminale del dominio elicasi, simile ad altri elicasi RecQ. Questo dominio è costituito da una regione-Zn vincolanti e un'elica alato (WH) dominio. Un'altra parte di questa tesi incentrata sulla caratterizzazione strutturale e biochimica del nucleo catalitico della RecQ4 compreso il elicasi e il dominio RQC. I risultati forniscono una descrizione nel Zn ligandi presenti nel dominio RQC che svolge un ruolo nel legame al DNA e l'attività svolgimento della proteina legante. Inoltre è stata stabilita la presenza della caratteristica residuo aromatico sulla punta della forcella WH β e il suo ruolo nel legame al DNA e di svolgimento. Infine, esso fornisce una bassa risoluzione SAXS modello del nucleo catalitico di RecQ4.
XXVII Ciclo
1985
Ren, Hua. « Aspects moléculaires des hélicases de la famille de RecQ ». Phd thesis, École normale supérieure de Cachan - ENS Cachan, 2009. http://tel.archives-ouvertes.fr/tel-00448084.
Texte intégralKaiser, Sebastian [Verfasser], et Caroline [Gutachter] Kisker. « A RecQ helicase in disguise : Characterization of the unconventional Structure and Function of the human Genome Caretaker RecQ4 / Sebastian Kaiser ; Gutachter : Caroline Kisker ». Würzburg : Universität Würzburg, 2019. http://d-nb.info/1206879246/34.
Texte intégralGuo, Rongbing. « Biochemical and structural characterization of BLM Helicase ». Paris 11, 2008. http://www.theses.fr/2008PA112168.
Texte intégralBloom's syndrome (BS) is an autosomal recessive disorder, showing high frequency of sister chromatid exchange in lymphocyte of the patients. Since BS is preposition of a wide spectrum of cancer, the syndrome has been studied for understanding of the mechanism of cancer extensively. Ln the first part, we proved the existence of a zinc-binding domain in which a zinc ion is coordinated by four cysteines residues in RecQ-Ct domain of BLM. This conclusion is drawn from our biophysical and biochemical studies. We modeled the 3D structure of BLM protein based on that of E. Coli RecQ helicase, which revealed a similar structural domain in both helicases that coordinate zinc. The results from experiments with three mutants showed that their enzymatic activities were severely reduced or abrogated. The demetalization of zinc from BLM had no influence on the activities of BLM, but it would decrease the themostability of the protein. Ln conclusion, BLM contains a zinc binding domain with one zinc ion in each protein. The second part of our studies includes the work for understanding of causative molecular mechanism of missense mutations which happened in helicase domain of BLM found in BS patients. On the basis of the work inthe fist part, we further modeled the 3D structure of BLM in complex with A TPyS and DNA. With the model, we deduced the possible causative mechanism of mutants. We produced mutant proteins and purified them to homogeneity. The A TPase activity, A TP binding activity, DNA binding activity and helicase activity ofthe mutants were ail checked. Ln conclusion 1 showed that: 1. BLM642-129o possibly employ an "inchworm" model mechanism; 2. Amino acid residues from 861 to 901 are imprtant for DNA binding; 3. DNA binding ofBLM is mainly controlled by lobe2 and lobe3, lobel contribute to a transient ssDNA binding; 4. The annealing activity of RecQ helicase suggests a weak DNA binding activity
Budhathoki, Jagat B. « Interactions of RecQ-Family Helicases with G-quadruplex Structures at the Single Molecule Level ». Kent State University / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=kent1467765011.
Texte intégralHuber, Michael D. « Structure-function analysis and substrate specific inhibition of RecQ helicases / ». Thesis, Connect to this title online ; UW restricted, 2005. http://hdl.handle.net/1773/9253.
Texte intégralBajpai, Sailesh. « Analysis of human RECQ1 helicase function in cells ». Thesis, Open University, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.522223.
Texte intégralLevitt, Nicola C. « Role of RecQ helicases in maintenance of genome integrity ». Thesis, University of Oxford, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.275469.
Texte intégralLucic, Bojana. « Understanding the structural basis of the human RECQ1 helicase function ». Thesis, Open University, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.536078.
Texte intégralLivres sur le sujet "RecQ4 helicases"
Lombard, David B. Biochemistry and genetics of recq-helicases. Boston, MA : Kluwer Academic Publishers, 2001.
Trouver le texte intégralLombard, David B. Biochemistry and Genetics of RecQ-Helicases. Boston, MA : Springer US, 2001. http://dx.doi.org/10.1007/978-1-4615-1405-3.
Texte intégralLombard, David B. Biochemistry and genetics of recq-helicases. Boston, MA : Kluwer Academic Publishers, 2001.
Trouver le texte intégralLombard, David B. Biochemistry and Genetics of RecQ-Helicases. Springer, 2012.
Trouver le texte intégralLombard, David B. Biochemistry and Genetics of Recq-Helicases. Springer London, Limited, 2012.
Trouver le texte intégralLombard, David B. Biochemistry and Genetics of RecQ-Helicases. Springer, 2000.
Trouver le texte intégralChapitres de livres sur le sujet "RecQ4 helicases"
Lombard, David B. « The RecQ-family helicases ». Dans Biochemistry and Genetics of RecQ-Helicases, 3–19. Boston, MA : Springer US, 2001. http://dx.doi.org/10.1007/978-1-4615-1405-3_1.
Texte intégralLu, Linchao, Weidong Jin, Hao Liu et Lisa L. Wang. « RECQ DNA Helicases and Osteosarcoma ». Dans Advances in Experimental Medicine and Biology, 129–45. Cham : Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-04843-7_7.
Texte intégralLu, Linchao, Weidong Jin et Lisa L. Wang. « RECQ DNA Helicases and Osteosarcoma ». Dans Current Advances in the Science of Osteosarcoma, 37–54. Cham : Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-43085-6_3.
Texte intégralMohaghegh, Payam, et Ian D. Hickson. « Biochemical Roles of RecQ Helicases ». Dans Molecular Mechanisms of Werner’s Syndrome, 12–21. Boston, MA : Springer US, 2004. http://dx.doi.org/10.1007/978-1-4419-9032-7_2.
Texte intégralLombard, David B. « Targeting the WRN Locus in the mouse ». Dans Biochemistry and Genetics of RecQ-Helicases, 21–41. Boston, MA : Springer US, 2001. http://dx.doi.org/10.1007/978-1-4615-1405-3_2.
Texte intégralLombard, David B. « Interaction of the BLM protein with Topo III alpha in Somatic and meiotic cells ». Dans Biochemistry and Genetics of RecQ-Helicases, 43–58. Boston, MA : Springer US, 2001. http://dx.doi.org/10.1007/978-1-4615-1405-3_3.
Texte intégralLombard, David B. « Nijmegen Breakage Syndrome disease protein and Mre11 at PML Nuclear Bodies and meiotic telomeres ». Dans Biochemistry and Genetics of RecQ-Helicases, 59–76. Boston, MA : Springer US, 2001. http://dx.doi.org/10.1007/978-1-4615-1405-3_4.
Texte intégralLarsen, Nicolai Balle, et Ian D. Hickson. « RecQ Helicases : Conserved Guardians of Genomic Integrity ». Dans Advances in Experimental Medicine and Biology, 161–84. New York, NY : Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-5037-5_8.
Texte intégralKobbe, Daniela, Manfred Focke et Holger Puchta. « Purification and Characterization of RecQ Helicases of Plants ». Dans Methods in Molecular Biology, 195–209. Totowa, NJ : Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-355-8_14.
Texte intégralSeki, Masayuki, Shusuke Tada et Takemi Enomoto. « Function of RECQ family helicase in genome stability ». Dans Subcellular Biochemistry, 49–73. Dordrecht : Springer Netherlands, 2006. http://dx.doi.org/10.1007/978-1-4020-4896-8_5.
Texte intégralActes de conférences sur le sujet "RecQ4 helicases"
Zuo, Mingxin, David Maxwell, Basvoju A. Bhanu Prasad, Zhenghong Peng, William Bornmann et Milind M. Javle. « Abstract 5361 : Development of targeted inhibitors against RecQ1 helicase ». Dans Proceedings : AACR Annual Meeting 2014 ; April 5-9, 2014 ; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.am2014-5361.
Texte intégralLao, Victoria Valinluck, Kelly T. Carter, Peter S. Rabinovitch, Piri Welcsh et William M. Grady. « Abstract 1157 : Increased expression of RecQ helicases in sporadic primary colorectal cancers ». Dans Proceedings : AACR 103rd Annual Meeting 2012‐‐ Mar 31‐Apr 4, 2012 ; Chicago, IL. American Association for Cancer Research, 2012. http://dx.doi.org/10.1158/1538-7445.am2012-1157.
Texte intégralChun, Stephen G., Nelson S. Yee, Fang Qi, Richard Allsopp, Philip M. Davy, Keith S. Fong, Michele Carbone et Peter K. Bryant-Greenwood. « Abstract 3209 : The WRN RecQ helicase acts as a tumor suppressor in pancreatic adenocarcinoma ». Dans Proceedings : AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010 ; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-3209.
Texte intégralWelcsh, Piri, Keffy Kehrli, Paul Lazarchuk et Julia Sidorova. « Abstract POSTER-BIOL-1346 : Growth-suppressive effect of WRN RECQ helicase inactivation in breast and ovarian cancer cells ». Dans Abstracts : 10th Biennial Ovarian Cancer Research Symposium ; September 8-9, 2014 ; Seattle, WA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1557-3265.ovcasymp14-poster-biol-1346.
Texte intégral