Literature DB >> 27748060

Developmental regulation of RNA processing by Rbfox proteins.

John G Conboy1.   

Abstract

The Rbfox genes encode an ancient family of sequence-specific RNA binding proteins (RBPs) that are critical developmental regulators in multiple tissues including skeletal muscle, cardiac muscle, and brain. The hallmark of Rbfox proteins is a single high-affinity RRM domain, highly conserved from insects to humans, that binds preferentially to UGCAUG motifs at diverse regulatory sites in pre-mRNA introns, mRNA 3'UTRs, and pre-miRNAs hairpin structures. Versatile regulatory circuits operate on Rbfox pre-mRNA and mRNA to ensure proper expression of Rbfox1 protein isoforms, which then act on the broader transcriptome to regulate alternative splicing networks, mRNA stability and translation, and microRNA processing. Complex Rbfox expression is encoded in large genes encompassing multiple promoters and alternative splicing options that govern spatiotemporal expression of structurally distinct and tissue-specific protein isoforms with different classes of RNA targets. Nuclear Rbfox1 is a candidate master regulator that binds intronic UGCAUG elements to impact splicing efficiency of target alternative exons, many in transcripts for other splicing regulators. Tissue-specificity of Rbfox-mediated alternative splicing is executed by combinatorial regulation through the integrated activity of Rbfox proteins and synergistic or antagonistic splicing factors. Studies in animal models show that Rbfox1-related genes are critical for diverse developmental processes including germ cell differentiation and memory in Drosophila, neuronal migration and function in mouse brain, myoblast fusion and skeletal muscle function, and normal heart function. Finally, genetic and biochemical evidence suggest that aberrations in Rbfox-regulated circuitry are risk factors for multiple human disorders, especially neurodevelopmental disorders including epilepsy and autism, and cardiac hypertrophy. WIREs RNA 2017, 8:e1398. doi: 10.1002/wrna.1398 For further resources related to this article, please visit the WIREs website.
© 2016 Wiley Periodicals, Inc.

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Year:  2016        PMID: 27748060      PMCID: PMC5315656          DOI: 10.1002/wrna.1398

Source DB:  PubMed          Journal:  Wiley Interdiscip Rev RNA        ISSN: 1757-7004            Impact factor:   9.957


  85 in total

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Authors:  Tugba Guven-Ozkan; Germain U Busto; Soleil S Schutte; Isaac Cervantes-Sandoval; Diane K O'Dowd; Ronald L Davis
Journal:  Cell Rep       Date:  2016-02-11       Impact factor: 9.423

2.  Molecular basis of RNA recognition by the human alternative splicing factor Fox-1.

Authors:  Sigrid D Auweter; Rudi Fasan; Luc Reymond; Jason G Underwood; Douglas L Black; Stefan Pitsch; Frédéric H-T Allain
Journal:  EMBO J       Date:  2005-12-15       Impact factor: 11.598

3.  Fox-2 splicing factor binds to a conserved intron motif to promote inclusion of protein 4.1R alternative exon 16.

Authors:  Julie L Ponthier; Christina Schluepen; Weiguo Chen; Robert A Lersch; Sherry L Gee; Victor C Hou; Annie J Lo; Sarah A Short; Joel A Chasis; John C Winkelmann; John G Conboy
Journal:  J Biol Chem       Date:  2006-03-14       Impact factor: 5.157

4.  MBNL1 and RBFOX2 cooperate to establish a splicing programme involved in pluripotent stem cell differentiation.

Authors:  Julian P Venables; Laure Lapasset; Gilles Gadea; Philippe Fort; Roscoe Klinck; Manuel Irimia; Emmanuel Vignal; Philippe Thibault; Panagiotis Prinos; Benoit Chabot; Sherif Abou Elela; Pierre Roux; Jean-Marc Lemaitre; Jamal Tazi
Journal:  Nat Commun       Date:  2013       Impact factor: 14.919

5.  Dysregulation of RBFOX2 Is an Early Event in Cardiac Pathogenesis of Diabetes.

Authors:  Curtis A Nutter; Elizabeth A Jaworski; Sunil K Verma; Vaibhav Deshmukh; Qiongling Wang; Olga B Botvinnik; Mario J Lozano; Ismail J Abass; Talha Ijaz; Allan R Brasier; Nisha J Garg; Xander H T Wehrens; Gene W Yeo; Muge N Kuyumcu-Martinez
Journal:  Cell Rep       Date:  2016-05-26       Impact factor: 9.423

6.  Pontocerebellar hypoplasia in association with de novo 19p13.11p13.12 microdeletion.

Authors:  Natalie M Gallant; Erin Baldwin; Noriko Salamon; Katrina M Dipple; Fabiola Quintero-Rivera
Journal:  Am J Med Genet A       Date:  2011-10-12       Impact factor: 2.802

7.  Defining the regulatory network of the tissue-specific splicing factors Fox-1 and Fox-2.

Authors:  Chaolin Zhang; Zuo Zhang; John Castle; Shuying Sun; Jason Johnson; Adrian R Krainer; Michael Q Zhang
Journal:  Genes Dev       Date:  2008-09-15       Impact factor: 11.361

8.  Molecular Features Underlying Neurodegeneration Identified through In Vitro Modeling of Genetically Diverse Parkinson's Disease Patients.

Authors:  Lin Lin; Jonathan Göke; Engin Cukuroglu; Mark R Dranias; Antonius M J VanDongen; Lawrence W Stanton
Journal:  Cell Rep       Date:  2016-06-02       Impact factor: 9.423

9.  Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants.

Authors:  Anthony J Griswold; Nicole D Dueker; Derek Van Booven; Joseph A Rantus; James M Jaworski; Susan H Slifer; Michael A Schmidt; William Hulme; Ioanna Konidari; Patrice L Whitehead; Michael L Cuccaro; Eden R Martin; Jonathan L Haines; John R Gilbert; John P Hussman; Margaret A Pericak-Vance
Journal:  Mol Autism       Date:  2015-07-07       Impact factor: 7.509

Review 10.  Fox-1 family of RNA-binding proteins.

Authors:  Hidehito Kuroyanagi
Journal:  Cell Mol Life Sci       Date:  2009-12       Impact factor: 9.261

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  43 in total

Review 1.  Genetic, epigenetic and posttranscriptional mechanisms for treatment of major depression: the 5-HT1A receptor gene as a paradigm

Authors:  Paul R. Albert; Brice Le François; Faranak Vahid-Ansari
Journal:  J Psychiatry Neurosci       Date:  2019-05-01       Impact factor: 6.186

2.  Dose-dependent action of the RNA binding protein FOX-1 to relay X-chromosome number and determine C. elegans sex.

Authors:  Behnom Farboud; Catherine S Novak; Monique Nicoll; Alyssa Quiogue; Barbara J Meyer
Journal:  Elife       Date:  2020-12-29       Impact factor: 8.140

Review 3.  When one becomes many-Alternative splicing in β-cell function and failure.

Authors:  Maria Inês Alvelos; Jonàs Juan-Mateu; Maikel Luis Colli; Jean-Valéry Turatsinze; Décio L Eizirik
Journal:  Diabetes Obes Metab       Date:  2018-09       Impact factor: 6.577

4.  Rbfox-1 contributes to CaMKIIα expression and intracerebral hemorrhage-induced secondary brain injury via blocking micro-RNA-124.

Authors:  Fang Shen; Xiang Xu; Zhengquan Yu; Haiying Li; Haitao Shen; Xiang Li; Meifen Shen; Gang Chen
Journal:  J Cereb Blood Flow Metab       Date:  2020-04-04       Impact factor: 6.200

5.  Aberrant Expression of a Non-muscle RBFOX2 Isoform Triggers Cardiac Conduction Defects in Myotonic Dystrophy.

Authors:  Chaitali Misra; Sushant Bangru; Feikai Lin; Kin Lam; Sara N Koenig; Ellen R Lubbers; Jamila Hedhli; Nathaniel P Murphy; Darren J Parker; Lawrence W Dobrucki; Thomas A Cooper; Emad Tajkhorshid; Peter J Mohler; Auinash Kalsotra
Journal:  Dev Cell       Date:  2020-02-27       Impact factor: 12.270

Review 6.  Cortical interneuron development: a tale of time and space.

Authors:  Jia Sheng Hu; Daniel Vogt; Magnus Sandberg; John L Rubenstein
Journal:  Development       Date:  2017-11-01       Impact factor: 6.868

7.  Splicing Activation by Rbfox Requires Self-Aggregation through Its Tyrosine-Rich Domain.

Authors:  Yi Ying; Xiao-Jun Wang; Celine K Vuong; Chia-Ho Lin; Andrey Damianov; Douglas L Black
Journal:  Cell       Date:  2017-07-13       Impact factor: 41.582

8.  Rbfox Splicing Factors Promote Neuronal Maturation and Axon Initial Segment Assembly.

Authors:  Martin Jacko; Sebastien M Weyn-Vanhentenryck; John W Smerdon; Rui Yan; Huijuan Feng; Damian J Williams; Joy Pai; Ke Xu; Hynek Wichterle; Chaolin Zhang
Journal:  Neuron       Date:  2018-02-01       Impact factor: 17.173

Review 9.  Faulty RNA splicing: consequences and therapeutic opportunities in brain and muscle disorders.

Authors:  Vittoria Pagliarini; Piergiorgio La Rosa; Claudio Sette
Journal:  Hum Genet       Date:  2017-04-22       Impact factor: 4.132

10.  Increased nuclear but not cytoplasmic activities of CELF1 protein leads to muscle wasting.

Authors:  Diana C Cox; Xiangnan Guan; Zheng Xia; Thomas A Cooper
Journal:  Hum Mol Genet       Date:  2020-06-27       Impact factor: 6.150

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