Regulatory Logic of Pan-Neuronal Gene Expression in C-elegans

被引:104
作者
Stefanakis, Nikolaos [1 ]
Carrera, Ines [1 ]
Hobert, Oliver [1 ]
机构
[1] Columbia Univ, Howard Hughes Med Inst, Med Ctr, Dept Biochem & Mol Biophys, New York, NY 10032 USA
基金
美国国家卫生研究院;
关键词
NEMATODE CAENORHABDITIS-ELEGANS; NERVOUS-SYSTEM; TERMINAL DIFFERENTIATION; CHEMOSENSORY NEURONS; HOMEODOMAIN PROTEIN; HOMEOBOX GENES; TRANSCRIPTION; IDENTITY; SPECIFICATION; SUPPRESSORS;
D O I
10.1016/j.neuron.2015.07.031
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
While neuronal cell types display an astounding degree of phenotypic diversity, most if not all neuron types share a core panel of terminal features. However, little is known about how pan-neuronal expression patterns are genetically programmed. Through an extensive analysis of the cis-regulatory control regions of a battery of pan-neuronal C. elegans genes, including genes involved in synaptic vesicle biology and neuropeptide signaling, we define a common organizational principle in the regulation of pan-neuronal genes in the form of a surprisingly complex array of seemingly redundant, parallel-acting cis-regulatory modules that direct expression to broad, overlapping domains throughout the nervous system. These parallel-acting cis-regulatory modules are responsive to a multitude of distinct trans-acting factors. Neuronal gene expression programs therefore fall into two fundamentally distinct classes. Neuron-type-specific genes are generally controlled by discrete and non-redundantly acting regulatory inputs, while pan-neuronal gene expression is controlled by diverse, coincident and seemingly redundant regulatory inputs.
引用
收藏
页码:733 / 750
页数:18
相关论文
共 43 条
[1]  
Altun-Gultekin Z, 2001, DEVELOPMENT, V128, P1951
[2]   Genetic ablation of Rest leads to in vitro-specific derepression of neuronal genes during neurogenesis [J].
Aoki, Hitomi ;
Hara, Akira ;
Era, Takumi ;
Kunisada, Takahiro ;
Yamada, Yasuhiro .
DEVELOPMENT, 2012, 139 (04) :667-677
[3]   A transcriptional regulatory cascade that controls left/right asymmetry in chemosensory neurons of C-elegans [J].
Chang, S ;
Johnston, RJ ;
Hobert, O .
GENES & DEVELOPMENT, 2003, 17 (17) :2123-2137
[4]   A RasGRP, C. elegans RGEF-1b, Couples External Stimuli to Behavior by Activating LET-60 (Ras) in Sensory Neurons [J].
Chen, Lu ;
Fu, Ya ;
Ren, Min ;
Xiao, Bing ;
Rubint, Charles S. .
NEURON, 2011, 70 (01) :51-65
[5]   NRSF/REST is required in vivo for repression of multiple neuronal target genes during embryogenesis [J].
Chen, ZF ;
Paquette, AJ ;
Anderson, DJ .
NATURE GENETICS, 1998, 20 (02) :136-142
[6]   A combinatorial regulatory signature controls terminal differentiation of the dopaminergic nervous system in C. elegans [J].
Doitsidou, Maria ;
Flames, Nuria ;
Topalidou, Irini ;
Abe, Namiko ;
Felton, Terry ;
Remesal, Laura ;
Popovitchenko, Tatiana ;
Mann, Richard ;
Chalfie, Martin ;
Hobert, Oliver .
GENES & DEVELOPMENT, 2013, 27 (12) :1391-1405
[7]  
Eastman C, 1999, J NEUROSCI, V19, P6225
[8]   Multiple layers of complexity in cis-regulatory regions of developmental genes [J].
Frankel, Nicolas .
DEVELOPMENTAL DYNAMICS, 2012, 241 (12) :1857-1866
[9]   A Competition Mechanism for a Homeotic Neuron Identity Transformation in C-elegans [J].
Gordon, Patricia M. ;
Hobert, Oliver .
DEVELOPMENTAL CELL, 2015, 34 (02) :206-219
[10]   PHA-1, A SELECTABLE MARKER FOR GENE-TRANSFER IN C-ELEGANS [J].
GRANATO, M ;
SCHNABEL, H ;
SCHNABEL, R .
NUCLEIC ACIDS RESEARCH, 1994, 22 (09) :1762-1763