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dc.contributor.authorTsutakawa, Susan E.
dc.contributor.authorTsai, Chi-Lin
dc.contributor.authorYan, Chunli
dc.contributor.authorBralic, Amer
dc.contributor.authorChazin, Walter J.
dc.contributor.authorHamdan, Samir
dc.contributor.authorSchärer, Orlando D.
dc.contributor.authorIvanov, Ivaylo
dc.contributor.authorTainer, John A.
dc.date.accessioned2020-10-01T11:44:21Z
dc.date.available2020-10-01T11:44:21Z
dc.date.issued2020-09-17
dc.date.submitted2020-07-10
dc.identifier.citationTsutakawa, S. E., Tsai, C.-L., Yan, C., Bralić, A., Chazin, W. J., Hamdan, S. M., … Tainer, J. A. (2020). Envisioning how the prototypic molecular machine TFIIH functions in transcription initiation and DNA repair. DNA Repair, 102972. doi:10.1016/j.dnarep.2020.102972
dc.identifier.issn1568-7864
dc.identifier.doi10.1016/j.dnarep.2020.102972
dc.identifier.urihttp://hdl.handle.net/10754/665400
dc.description.abstractCritical for transcription initiation and bulky lesion DNA repair, TFIIH provides an exemplary system to connect molecular mechanisms to biological outcomes due to its strong genetic links to different specific human diseases. Recent advances in structural and computational biology provide a unique opportunity to re-examine biologically relevant molecular structures and develop possible mechanistic insights for the large dynamic TFIIH complex. TFIIH presents many puzzles involving how its two SF2 helicase family enzymes, XPB and XPD, function in transcription initiation and repair: how do they initiate transcription, detect and verify DNA damage, select the damaged strand for incision, coordinate repair with transcription and cell cycle through Cdkactivating-kinase (CAK) signaling, and result in very different specific human diseases associated with cancer, aging, and development from single missense mutations? By joining analyses of breakthrough cryo-electron microscopy (cryo-EM) structures and advanced computation with data from biochemistry and human genetics, we develop unified concepts and molecular level understanding for TFIIH functions with a focus on structural mechanisms. We provocatively consider that TFIIH may have first evolved from evolutionary pressure for TCR to resolve arrested transcription blocks to DNA replication and later added its key roles in transcription initiation and global DNA repair. We anticipate that this level of mechanistic information will have significant impact on thinking about TFIIH, laying a robust foundation suitable to develop new paradigms for DNA transcription initiation and repair along with insights into disease prevention, susceptibility, diagnosis and interventions.
dc.description.sponsorshipWe thank the researchers, patients, and families who have critically contributed to defining the genetic basis for TFIIH pathophysiology. Work on TFIIH is supported by NCI P01 CA092584 (to S.E.T., O.D.S, W. J.C., I.I., J.A.T.), R01 CA218315 (to O.D.S., W.J.C.), NCI R35 CA220430 (to J.A.T.); NIGMS R01GM110387 (to S.E.T. and I.I.); and KAUST CRG3 (to S.M.H and J.A.T.). J.A.T. is a CPRIT Scholar in Cancer Research and acknowledges support by a Robert A. Welch Chemistry Chair. The O.D.S. laboratory is supported by the Korean Institute of Basic Science IBSR022-A1. I.I. acknowledges computational resources for TFIIH analysis provided by the NSF XSEDE programCHE110042 and the ORNL INCITE program under DOEDE-AC05-00OR22725.
dc.publisherElsevier BV
dc.relation.urlhttps://linkinghub.elsevier.com/retrieve/pii/S1568786420302214
dc.rightsThis is an open access article under the CC BY-NC-ND license.
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.titleEnvisioning how the prototypic molecular machine TFIIH functions in transcription initiation and DNA repair
dc.typeArticle
dc.contributor.departmentBiological and Environmental Sciences and Engineering (BESE) Division
dc.contributor.departmentBioscience Program
dc.contributor.departmentLaboratory of DNA Replication and Recombination
dc.identifier.journalDNA Repair
dc.eprint.versionPublisher's Version/PDF
dc.contributor.institutionMolecular Biophysics and Integrated Bioimaging, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, USA .
dc.contributor.institutionDepartment of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
dc.contributor.institutionDepartment of Chemistry, Georgia State University, Atlanta, GA, 30302 USA.
dc.contributor.institutionCenter for Diagnostics and Therapeutics, Georgia State University, Atlanta, GA, 30302 USA.
dc.contributor.institutionDepartments of Biochemistry and Chemistry, and Center for Structural Biology, Vanderbilt University, Nashville, TN, 37240, USA.
dc.contributor.institutionCenter for Genomic Integrity, Institute for Basic Science, Ulsan 44919, Republic of Korea.
dc.contributor.institutionSchool of Life Sciences, Ulsan National Institute of Science and Technology, Ulsan, 44919, Republic of Korea.
dc.contributor.institutionDepartment of Cancer Biology, University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
dc.identifier.pages102972
kaust.personBralic, Amer
kaust.personHamdan, Samir
kaust.grant.numberCRG3
dc.date.accepted2020-09-07
refterms.dateFOA2020-10-01T11:45:11Z
dc.date.published-online2020-09-17
dc.date.published-print2020-12


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