DNA double-strand breaks as drivers of neural genomic change, function, and disease

被引:72
作者
Alt, Frederick W. [1 ,2 ]
Schwer, Bjoern [3 ,4 ]
机构
[1] Harvard Med Sch, Howard Hughes Med Inst, Program Cellular & Mol Med, Dept Genet,Boston Childrens Hosp, Boston, MA 02115 USA
[2] Harvard Med Sch, Dept Pediat, Boston, MA 02115 USA
[3] Univ Calif San Francisco, Dept Neurol Surg, San Francisco, CA 94158 USA
[4] Univ Calif San Francisco, Eli & Edythe Broad Ctr Regenerat Med & Stem Cell, San Francisco, CA 94158 USA
关键词
DNA repair; Non-homologous end joining; DNA double-strand breaks; Neural stem and progenitor cells; Neurons; Somatic mosaicism; Exon shuffling; Genomic instability; DNA replication; Transcription; Neurodevelopment; Copy number variations; END-JOINING PROTEINS; COMMON FRAGILE SITES; V(D)J RECOMBINATION; NERVOUS-SYSTEM; CHROMOSOMAL TRANSLOCATIONS; STEM/PROGENITOR CELLS; EMBRYONIC LETHALITY; SEQUENCING REVEALS; LIGASE IV; B-CELLS;
D O I
10.1016/j.dnarep.2018.08.019
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Early work from about two decades ago implicated DNA double-strand break (DSB) formation and repair in neuronal development. Findings emerging from recent studies of DSBs in proliferating neural progenitors and in mature, non-dividing neurons suggest important roles of DSBs in brain physiology, aging, cancer, psychiatric and neurodegenerative disorders. We provide an overview of some findings and speculate on what may lie ahead.
引用
收藏
页码:158 / 163
页数:6
相关论文
共 74 条
[1]  
Alt FW, 2017, RES PER NEUROSCI, P63, DOI 10.1007/978-3-319-60192-2_6
[2]   Mechanisms of Programmed DNA Lesions and Genomic Instability in the Immune System [J].
Alt, Frederick W. ;
Zhang, Yu ;
Meng, Fei-Long ;
Guo, Chunguang ;
Schwer, Bjoern .
CELL, 2013, 152 (03) :417-429
[3]   JOINING OF IMMUNOGLOBULIN HEAVY-CHAIN GENE SEGMENTS - IMPLICATIONS FROM A CHROMOSOME WITH EVIDENCE OF 3 D-JH FUSIONS [J].
ALT, FW ;
BALTIMORE, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (13) :4118-4122
[4]   DNA Break Mapping Reveals Topoisomerase II Activity Genome-Wide [J].
Baranello, Laura ;
Kouzine, Fedor ;
Wojtowicz, Damian ;
Cui, Kairong ;
Przytycka, Teresa M. ;
Zhao, Keji ;
Levens, David .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2014, 15 (07) :13111-13122
[5]   Identification of Early Replicating Fragile Sites that Contribute to Genome Instability [J].
Barlow, Jacqueline H. ;
Faryabi, Robert B. ;
Callen, Elsa ;
Wong, Nancy ;
Malhowski, Amy ;
Chen, Hua Tang ;
Gutierrez-Cruz, Gustavo ;
Sun, Hong-Wei ;
McKinnon, Peter ;
Wright, George ;
Casellas, Rafael ;
Robbiani, Davide F. ;
Staudt, Louis ;
Fernandez-Capetillo, Oscar ;
Nussenzweig, Andre .
CELL, 2013, 152 (03) :620-632
[6]   Classical and Alternative End-Joining Pathways for Repair of Lymphocyte-Specific and General DNA Double-Strand Breaks [J].
Boboila, Cristian ;
Alt, Frederick W. ;
Schwer, Bjoern .
ADVANCES IN IMMUNOLOGY, VOL 116, 2012, 116 :1-49
[7]   Transcriptional elongation requires DNA break-induced signalling [J].
Bunch, Heeyoun ;
Lawney, Brian P. ;
Lin, Yu-Fen ;
Asaithamby, Aroumougame ;
Murshid, Ayesha ;
Wang, Yaoyu E. ;
Chen, Benjamin P. C. ;
Calderwood, Stuart K. .
NATURE COMMUNICATIONS, 2015, 6
[8]   A critical role for topoisomerase IIb and DNA double strand breaks in transcription [J].
Calderwood, Stuart K. .
TRANSCRIPTION-AUSTIN, 2016, 7 (03) :75-83
[9]   Genome Organization Drives Chromosome Fragility [J].
Canela, Andres ;
Maman, Yaakov ;
Jung, Seolkyoung ;
Wong, Nancy ;
Callen, Elsa ;
Day, Amanda ;
Kieffer-Kwon, Kyong-Rim ;
Pekowska, Aleksandra ;
Zhang, Hongliang ;
Rao, Suhas S. P. ;
Huang, Su-Chen ;
Mckinnon, Peter J. ;
Aplan, Peter D. ;
Pommier, Yves ;
Aiden, Erez Lieberman ;
Casellas, Rafael ;
Nussenzweig, Andre .
CELL, 2017, 170 (03) :507-+
[10]   Non-homologous DNA end joining and alternative pathways to double-strand break repair [J].
Chang, Howard H. Y. ;
Pannunzio, Nicholas R. ;
Adachi, Noritaka ;
Lieber, Michael R. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2017, 18 (08) :495-506