Transcribing the connectome: roles for transcription factors and chromatin regulators in activity-dependent synapse development

被引:20
作者
Chen, Liang-Fu [1 ]
Zhou, Allen S. [1 ]
West, Anne E. [1 ]
机构
[1] Duke Univ, Dept Neurobiol, Durham, NC USA
关键词
activity-dependent synaptic plasticity; autism; chromatin; synapse development; transcription; AUTISM SPECTRUM DISORDER; CPG-BINDING PROTEIN-2; MENTAL-RETARDATION PROTEIN; DE-NOVO MUTATIONS; RETT-SYNDROME; MEF2C HAPLOINSUFFICIENCY; BDNF TRANSCRIPTION; IN-VIVO; NEURAL DEVELOPMENT; DNA-METHYLATION;
D O I
10.1152/jn.00067.2017
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The wiring of synaptic connections in the developing mammalian brain is shaped by both intrinsic and extrinsic signals. One point where these regulatory pathways converge is via the sensory experience-dependent regulation of new gene transcription. Recent studies have elucidated a number of molecular mechanisms that allow nuclear transcription factors and chromatin regulatory proteins to encode aspects of specificity in experience-dependent synapse development. Here we review the evidence for the transcriptional mechanisms that sculpt activity-dependent aspects of synaptic connectivity during postnatal development and discuss how disruption of these processes is associated with aberrant brain development in autism and intellectual disability.
引用
收藏
页码:755 / 770
页数:16
相关论文
共 141 条
[1]   Advances in autism genetics: on the threshold of a new neurobiology [J].
Abrahams, Brett S. ;
Geschwind, Daniel H. .
NATURE REVIEWS GENETICS, 2008, 9 (05) :341-355
[2]   Dendrite development regulated by CREST, a calcium-regulated transcriptional activator [J].
Aizawa, H ;
Hu, SC ;
Bobb, K ;
Balakrishnan, K ;
Ince, G ;
Gurevich, I ;
Cowan, M ;
Ghosh, A .
SCIENCE, 2004, 303 (5655) :197-202
[3]   Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 [J].
Amir, RE ;
Van den Veyver, IB ;
Wan, M ;
Tran, CQ ;
Francke, U ;
Zoghbi, HY .
NATURE GENETICS, 1999, 23 (02) :185-188
[4]   Neuropathology of Rett syndrome [J].
Armstrong, DD .
JOURNAL OF CHILD NEUROLOGY, 2005, 20 (09) :747-753
[5]   Evolution of Osteocrin as an activity-regulated factor in the primate brain [J].
Ataman, Bulent ;
Boulting, Gabriella L. ;
Harmin, David A. ;
Yang, Marty G. ;
Baker-Salisbury, Mollie ;
Yap, Ee-Lynn ;
Malik, Athar N. ;
Mei, Kevin ;
Rubin, Alex A. ;
Spiegel, Ivo ;
Durresi, Ershela ;
Sharma, Nikhil ;
Hu, Linda S. ;
Pletikos, Mihovil ;
Griffith, Eric C. . ;
Partlow, Jennifer N. ;
Stevens, Christine R. ;
Adli, Mazhar ;
Chahrour, Maria ;
Sestan, Nenad ;
Walsh, Christopher A. ;
Berezovskii, Vladimir K. ;
Livingstone, Margaret S. ;
Greenberg, Michael E. .
NATURE, 2016, 539 (7628) :242-+
[6]   An AT-Hook Domain in MeCP2 Determines the Clinical Course of Rett Syndrome and Related Disorders [J].
Baker, Steven Andrew ;
Chen, Lin ;
Wilkins, Angela Dawn ;
Yu, Peng ;
Lichtarge, Olivier ;
Zoghbi, Huda Yahya .
CELL, 2013, 152 (05) :984-996
[7]   MEF2C, a transcription factor that facilitates learning and memory by negative regulation of synapse numbers and function [J].
Barbosa, Ana C. ;
Kim, Mi-Sung ;
Ertunc, Mert ;
Adachi, Megumi ;
Nelson, Erika D. ;
McAnally, John ;
Richardson, James A. ;
Kavalali, Ege T. ;
Monteggia, Lisa M. ;
Bassel-Duby, Rhonda ;
Olson, Eric N. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (27) :9391-9396
[8]   From the connectome to brain function [J].
Bargmann, Cornelia I. ;
Marder, Eve .
NATURE METHODS, 2013, 10 (06) :483-490
[9]   Fragile X Syndrome: Loss of Local mRNA Regulation Alters Synaptic Development and Function [J].
Bassell, Gary J. ;
Warren, Stephen T. .
NEURON, 2008, 60 (02) :201-214
[10]   Widespread Changes in Dendritic and Axonal Morphology in Mecp2-Mutant Mouse Models of Rett Syndrome: Evidence for Disruption of Neuronal Networks [J].
Belichenko, Pavel V. ;
Wright, Elena E. ;
Belichenko, Nadia P. ;
Masliah, Eliezer ;
Li, Hong Hua ;
Mobley, William C. ;
Francke, Uta .
JOURNAL OF COMPARATIVE NEUROLOGY, 2009, 514 (03) :240-258