The Physiological Roles of the Exon Junction Complex in Development and Diseases

被引:15
作者
Asthana, Shravan [1 ]
Martin, Hannah [1 ]
Rupkey, Julian [1 ]
Patel, Shray [1 ]
Yoon, Joy [1 ]
Keegan, Abiageal [1 ]
Mao, Yingwei [1 ]
机构
[1] Penn State Univ, Dept Biol, University Pk, PA 16802 USA
基金
美国国家卫生研究院;
关键词
RBM8A; MAGOH; MLN51; neurodevelopment; NMD; mRNA; MESSENGER-RNA DECAY; NONSENSE-MEDIATED DECAY; CHILDHOOD-ONSET SCHIZOPHRENIA; MAGO NASHI; BINDING PROTEIN; GENE-EXPRESSION; CORE COMPLEX; ENHANCES TRANSLATION; STRUCTURAL INSIGHTS; REVEALS;
D O I
10.3390/cells11071192
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The exon junction complex (EJC) becomes an increasingly important regulator of early gene expression in the central nervous system (CNS) and other tissues. The EJC is comprised of three core proteins: RNA-binding motif 8A (RBM8A), Mago homolog (MAGOH), eukaryotic initiation factor 4A3 (EIF4A3), and a peripheral EJC factor, metastatic lymph node 51 (MLN51), together with various auxiliary factors. The EJC is assembled specifically at exon-exon junctions on mRNAs, hence the name of the complex. The EJC regulates multiple levels of gene expression, from splicing to translation and mRNA degradation. The functional roles of the EJC have been established as crucial to the normal progress of embryonic and neurological development, with wide ranging implications on molecular, cellular, and organism level function. Dysfunction of the EJC has been implicated in multiple developmental and neurological diseases. In this review, we discuss recent progress on the EJC's physiological roles.
引用
收藏
页数:17
相关论文
共 169 条
[1]   A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders [J].
Addington, A. M. ;
Gauthier, J. ;
Piton, A. ;
Hamdan, F. F. ;
Raymond, A. ;
Gogtay, N. ;
Miller, R. ;
Tossell, J. ;
Bakalar, J. ;
Germain, G. ;
Gochman, P. ;
Long, R. ;
Rapoport, J. L. ;
Rouleau, G. A. .
MOLECULAR PSYCHIATRY, 2011, 16 (03) :238-239
[2]   An EJC Factor RBM8a Regulates Anxiety Behaviors [J].
Alachkar, A. ;
Jiang, D. ;
Harrison, M. ;
Zhou, Y. ;
Chen, G. ;
Mao, Y. .
CURRENT MOLECULAR MEDICINE, 2013, 13 (06) :887-899
[3]   Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome [J].
Albers, Cornelis A. ;
Paul, Dirk S. ;
Schulze, Harald ;
Freson, Kathleen ;
Stephens, Jonathan C. ;
Smethurst, Peter A. ;
Jolley, Jennifer D. ;
Cvejic, Ana ;
Kostadima, Myrto ;
Bertone, Paul ;
Breuning, Martijn H. ;
Debili, Najet ;
Deloukas, Panos ;
Favier, Remi ;
Fiedler, Janine ;
Hobbs, Catherine M. ;
Huang, Ni ;
Hurles, Matthew E. ;
Kiddle, Graham ;
Krapels, Ingrid ;
Nurden, Paquita ;
Ruivenkamp, Claudia A. L. ;
Sambrook, Jennifer G. ;
Smith, Kenneth ;
Stemple, Derek L. ;
Strauss, Gabriele ;
Thys, Chantal ;
van Geet, Chris ;
Newbury-Ecob, Ruth ;
Ouwehand, Willem H. ;
Ghevaert, Cedric .
NATURE GENETICS, 2012, 44 (04) :435-U248
[4]   Human spliceosomal protein CWC22 plays a role in coupling splicing to exon junction complex deposition and nonsense-mediated decay [J].
Alexandrov, Andrei ;
Colognori, David ;
Shu, Mei-Di ;
Steitz, Joan A. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (52) :21313-21318
[5]   Full UPF3B function is critical for neuronal differentiation of neural stem cells [J].
Alrahbeni, Tahani ;
Sartor, Francesca ;
Anderson, Jihan ;
Miedzybrodzka, Zosia ;
McCaig, Colin ;
Mueller, Berndt .
MOLECULAR BRAIN, 2015, 8
[6]   Structure of the exon junction core complex with a trapped DEAD-box ATPase bound to RNA [J].
Andersen, Christian B. F. ;
Ballut, Lionel ;
Johansen, Jesper S. ;
Chamieh, Hala ;
Nielsen, Klaus H. ;
Oliveira, Cristiano L. P. ;
Pedersen, Jan Skov ;
Seraphin, Bertrand ;
Le Hir, Herve ;
Andersen, Gregers Rom .
SCIENCE, 2006, 313 (5795) :1968-1972
[7]   Mechanism of Nonsense-Mediated mRNA Decay Stimulation by Splicing Factor SRSF1 [J].
Aznarez, Isabel ;
Nomakuchi, Tomoki T. ;
Tetenbaum-Novatt, Jaclyn ;
Rahman, Mohammad Alinoor ;
Fregoso, Oliver ;
Rees, Holly ;
Krainer, Adrian R. .
CELL REPORTS, 2018, 23 (07) :2186-2198
[8]   The exon-junction-complex-component metastatic lymph node 51 functions in stress-granule assembly [J].
Baguet, Aurelie ;
Degot, Sebastien ;
Cougot, Nicolas ;
Bertrand, Edouard ;
Chenard, Marie-Pierre ;
Wendling, Corinne ;
Kessler, Pascal ;
Le Hir, Herve ;
Rio, Marie-Christine ;
Tomasetto, Catherine .
JOURNAL OF CELL SCIENCE, 2007, 120 (16) :2774-2784
[9]   The exon junction core complex is locked onto RNA by inhibition of eIF4AIII ATPase activity [J].
Ballut, L ;
Marchadier, B ;
Baguet, A ;
Tomasetto, C ;
Séraphin, B ;
Le Hir, H .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2005, 12 (10) :861-869
[10]   UPF2, a nonsense-mediated mRNA decay factor, is required for prepubertal Sertoli cell development and male fertility by ensuring fidelity of the transcriptome [J].
Bao, Jianqiang ;
Tang, Chong ;
Yuan, Shuiqiao ;
Porse, Bo T. ;
Yan, Wei .
DEVELOPMENT, 2015, 142 (02) :352-362