Literature DB >> 31602609

Advanced Methods for the Analysis of Altered Pre-mRNA Splicing in Yeast and Disease.

Huw B Thomas1, Raymond T O'Keefe2.   

Abstract

Splicing of pre-messenger RNA (pre-mRNA) transcripts is a fundamental process in all eukaryotes that provides a mechanism of increasing the proteomic diversity within a cell that can be tightly regulated in a dynamic manner. While constitutive and alternative splicing are necessary for the correct development and regulation of cells/organisms, aberrant splicing is now associated with an increasingly varied number of human diseases, such as neurological and developmental diseases, and cancer. Studies of splicing mechanisms and regulation are often achieved in nonhuman model organisms such as yeast. Yeasts possess homologs to many of the core spliceosome components of higher organisms, including humans, and as such yeast species are now a well-established model organism for understanding how differential splicing of transcripts can alter the phenotype of a cell or organism. Here we describe methods to investigate pre-mRNA splicing in yeast cells using modern RNA-Seq technology and bioinformatics software. Details of traditional validation methods are also described.

Entities:  

Keywords:  Pre-mRNA splicing; RNA-Seq; Spliceosome; Yeast

Mesh:

Substances:

Year:  2019        PMID: 31602609     DOI: 10.1007/978-1-4939-9736-7_8

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  16 in total

1.  Haploinsufficiency of a spliceosomal GTPase encoded by EFTUD2 causes mandibulofacial dysostosis with microcephaly.

Authors:  Matthew A Lines; Lijia Huang; Jeremy Schwartzentruber; Stuart L Douglas; Danielle C Lynch; Chandree Beaulieu; Maria Leine Guion-Almeida; Roseli Maria Zechi-Ceide; Blanca Gener; Gabriele Gillessen-Kaesbach; Caroline Nava; Geneviève Baujat; Denise Horn; Usha Kini; Almuth Caliebe; Yasemin Alanay; Gulen Eda Utine; Dorit Lev; Jürgen Kohlhase; Arthur W Grix; Dietmar R Lohmann; Ute Hehr; Detlef Böhm; Jacek Majewski; Dennis E Bulman; Dagmar Wieczorek; Kym M Boycott
Journal:  Am J Hum Genet       Date:  2012-02-02       Impact factor: 11.025

Review 2.  The role of Snu114p during pre-mRNA splicing.

Authors:  Lily Novak Frazer; Verity Nancollis; Raymond T O'Keefe
Journal:  Biochem Soc Trans       Date:  2008-06       Impact factor: 5.407

3.  Extensive cryptic splicing upon loss of RBM17 and TDP43 in neurodegeneration models.

Authors:  Qiumin Tan; Hari Krishna Yalamanchili; Jeehye Park; Antonia De Maio; Hsiang-Chih Lu; Ying-Wooi Wan; Joshua J White; Vitaliy V Bondar; Layal S Sayegh; Xiuyun Liu; Yan Gao; Roy V Sillitoe; Harry T Orr; Zhandong Liu; Huda Y Zoghbi
Journal:  Hum Mol Genet       Date:  2016-12-01       Impact factor: 6.150

4.  Compound heterozygosity of low-frequency promoter deletions and rare loss-of-function mutations in TXNL4A causes Burn-McKeown syndrome.

Authors:  Dagmar Wieczorek; William G Newman; Thomas Wieland; Tea Berulava; Maria Kaffe; Daniela Falkenstein; Christian Beetz; Elisabeth Graf; Thomas Schwarzmayr; Sofia Douzgou; Jill Clayton-Smith; Sarah B Daly; Simon G Williams; Sanjeev S Bhaskar; Jill E Urquhart; Beverley Anderson; James O'Sullivan; Odile Boute; Jasmin Gundlach; Johanna Christina Czeschik; Anthonie J van Essen; Filiz Hazan; Sarah Park; Anne Hing; Alma Kuechler; Dietmar R Lohmann; Kerstin U Ludwig; Elisabeth Mangold; Laura Steenpaß; Michael Zeschnigk; Johannes R Lemke; Charles Marques Lourenco; Ute Hehr; Eva-Christina Prott; Melanie Waldenberger; Anne C Böhmer; Bernhard Horsthemke; Raymond T O'Keefe; Thomas Meitinger; John Burn; Hermann-Josef Lüdecke; Tim M Strom
Journal:  Am J Hum Genet       Date:  2014-11-26       Impact factor: 11.025

Review 5.  Prp8 protein: at the heart of the spliceosome.

Authors:  Richard J Grainger; Jean D Beggs
Journal:  RNA       Date:  2005-05       Impact factor: 4.942

Review 6.  Brr2p RNA helicase with a split personality: insights into structure and function.

Authors:  Daniela Hahn; Jean D Beggs
Journal:  Biochem Soc Trans       Date:  2010-08       Impact factor: 5.407

7.  Mutations in SNRPB, encoding components of the core splicing machinery, cause cerebro-costo-mandibular syndrome.

Authors:  Séverine Bacrot; Mathilde Doyard; Céline Huber; Olivier Alibeu; Niklas Feldhahn; Daphné Lehalle; Didier Lacombe; Sandrine Marlin; Patrick Nitschke; Florence Petit; Marie-Paule Vazquez; Arnold Munnich; Valérie Cormier-Daire
Journal:  Hum Mutat       Date:  2014-12-11       Impact factor: 4.878

8.  Autosomal-dominant retinitis pigmentosa caused by a mutation in SNRNP200, a gene required for unwinding of U4/U6 snRNAs.

Authors:  Chen Zhao; Deepti L Bellur; Shasha Lu; Feng Zhao; Michael A Grassi; Sara J Bowne; Lori S Sullivan; Stephen P Daiger; Li Jia Chen; Chi Pui Pang; Kanxing Zhao; Jonathan P Staley; Catharina Larsson
Journal:  Am J Hum Genet       Date:  2009-10-29       Impact factor: 11.025

9.  Alternative Splicing of EZH2 pre-mRNA by SF3B3 Contributes to the Tumorigenic Potential of Renal Cancer.

Authors:  Ke Chen; Haibing Xiao; Jin Zeng; Gan Yu; Hui Zhou; Chunhua Huang; Weimin Yao; Wei Xiao; Junhui Hu; Wei Guan; Lily Wu; Jiaoti Huang; Qihong Huang; Hua Xu; Zhangqun Ye
Journal:  Clin Cancer Res       Date:  2016-11-22       Impact factor: 12.531

10.  RNA-seq reveals activation of both common and cytokine-specific pathways following neutrophil priming.

Authors:  Helen L Wright; Huw B Thomas; Robert J Moots; Steven W Edwards
Journal:  PLoS One       Date:  2013-03-06       Impact factor: 3.240

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