Literature DB >> 34104971

Transcript isoforms of Reep6 have distinct functions in the retina.

Qingnan Liang1,2, Nathaniel Wu1, Smriti Zaneveld1, Hehe Liu1, Shangyi Fu1, Keqing Wang1, Renae Bertrand1,2, Jun Wang1, Yumei Li1, Rui Chen1,2.   

Abstract

Much of the complexity of the eukaryotic cell transcriptome is due to the alternative splicing of mRNA. However, knowledge on how transcriptome complexity is translated into functional complexity remains limited. For example, although different isoforms of a gene may show distinct temporal and spatial expression patterns, it is largely unknown whether these isoforms encode proteins with distinct functions matching their expression pattern. In this report, we investigated the function and relationship of the two isoforms of Reep6, namely Reep6.1 and Reep6.2, in rod photoreceptor cells. These two isoforms result from the alternative splicing of exon 5 and show mutually exclusive expression patterns. Reep6.2 is the canonical isoform that is expressed in non-retinal tissues, whereas Reep6.1 is the only expressed isoform in the adult retina. The Reep6.1 isoform-specific knockout mouse, Reep6E5/E5, is generated by deleting exon 5 and a homozygous deletion phenotypically displayed a rod degeneration phenotype comparable to a Reep6 full knockout mouse, indicating that the Reep6.1 isoform is essential for the rod photoreceptor cell survival. Consistent with the results obtained from a loss-of-function experiment, overexpression of Reep6.2 failed to rescue the rod degeneration phenotype of Reep6 knockout mice whereas overexpression of Reep6.1 does lead to rescue. These results demonstrate that, consistent with the expression pattern of the isoform, Reep6.1 has rod-specific functions that cannot be substituted by its canonical isoform. Our findings suggested that a strict regulation of splicing is required for the maintenance of photoreceptor cells.
© The Author(s) 2021. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

Entities:  

Mesh:

Substances:

Year:  2021        PMID: 34104971      PMCID: PMC8522633          DOI: 10.1093/hmg/ddab157

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   5.121


  38 in total

Review 1.  Function of alternative splicing.

Authors:  Olga Kelemen; Paolo Convertini; Zhaiyi Zhang; Yuan Wen; Manli Shen; Marina Falaleeva; Stefan Stamm
Journal:  Gene       Date:  2012-08-15       Impact factor: 3.688

2.  A spastic paraplegia mouse model reveals REEP1-dependent ER shaping.

Authors:  Christian Beetz; Nicole Koch; Mukhran Khundadze; Geraldine Zimmer; Sandor Nietzsche; Nicole Hertel; Antje-Kathrin Huebner; Rizwan Mumtaz; Michaela Schweizer; Elisabeth Dirren; Kathrin N Karle; Andrey Irintchev; Victoria Alvarez; Christoph Redies; Martin Westermann; Ingo Kurth; Thomas Deufel; Michael M Kessels; Britta Qualmann; Christian A Hübner
Journal:  J Clin Invest       Date:  2013-09-24       Impact factor: 14.808

3.  Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13).

Authors:  A B McKie; J C McHale; T J Keen; E E Tarttelin; R Goliath; J J van Lith-Verhoeven; J Greenberg; R S Ramesar; C B Hoyng; F P Cremers; D A Mackey; S S Bhattacharya; A C Bird; A F Markham; C F Inglehearn
Journal:  Hum Mol Genet       Date:  2001-07-15       Impact factor: 6.150

4.  Hereditary spastic paraplegia proteins REEP1, spastin, and atlastin-1 coordinate microtubule interactions with the tubular ER network.

Authors:  Seong H Park; Peng-Peng Zhu; Rell L Parker; Craig Blackstone
Journal:  J Clin Invest       Date:  2010-04       Impact factor: 14.808

5.  Transcriptional expression of cis-acting and trans-acting splicing mutations cause autosomal dominant retinitis pigmentosa.

Authors:  María José Gamundi; Imma Hernan; Marta Muntanyola; Miquel Maseras; Pedro López-Romero; Rebeca Alvarez; Ana Dopazo; Salud Borrego; Miguel Carballo
Journal:  Hum Mutat       Date:  2008-06       Impact factor: 4.878

Review 6.  Alternative splicing and retinal degeneration.

Authors:  M M Liu; D J Zack
Journal:  Clin Genet       Date:  2013-06-05       Impact factor: 4.438

7.  Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa.

Authors:  Gavin Arno; Smriti A Agrawal; Aiden Eblimit; James Bellingham; Mingchu Xu; Feng Wang; Christina Chakarova; David A Parfitt; Amelia Lane; Thomas Burgoyne; Sarah Hull; Keren J Carss; Alessia Fiorentino; Matthew J Hayes; Peter M Munro; Ralph Nicols; Nikolas Pontikos; Graham E Holder; Chinwe Asomugha; F Lucy Raymond; Anthony T Moore; Vincent Plagnol; Michel Michaelides; Alison J Hardcastle; Yumei Li; Catherine Cukras; Andrew R Webster; Michael E Cheetham; Rui Chen
Journal:  Am J Hum Genet       Date:  2016-11-23       Impact factor: 11.025

8.  REEP6 deficiency leads to retinal degeneration through disruption of ER homeostasis and protein trafficking.

Authors:  Smriti A Agrawal; Thomas Burgoyne; Aiden Eblimit; James Bellingham; David A Parfitt; Amelia Lane; Ralph Nichols; Chinwe Asomugha; Matthew J Hayes; Peter M Munro; Mingchu Xu; Keqing Wang; Clare E Futter; Yumei Li; Rui Chen; Michael E Cheetham
Journal:  Hum Mol Genet       Date:  2017-07-15       Impact factor: 6.150

9.  Alternative isoform regulation in human tissue transcriptomes.

Authors:  Eric T Wang; Rickard Sandberg; Shujun Luo; Irina Khrebtukova; Lu Zhang; Christine Mayr; Stephen F Kingsmore; Gary P Schroth; Christopher B Burge
Journal:  Nature       Date:  2008-11-27       Impact factor: 49.962

Review 10.  Alternative Splicing in Neurogenesis and Brain Development.

Authors:  Chun-Hao Su; Dhananjaya D; Woan-Yuh Tarn
Journal:  Front Mol Biosci       Date:  2018-02-12
View more
  4 in total

Review 1.  Exploring the eukaryotic Yip and REEP/Yop superfamily of membrane-shaping adapter proteins (MSAPs): A cacophony or harmony of structure and function?

Authors:  Timothy Angelotti
Journal:  Front Mol Biosci       Date:  2022-08-19

2.  Identification of the Transcriptional Biomarkers Panel Linked to Pathological Remodelling of the Eye Tissues in Various HD Mouse Models.

Authors:  Iwona Mazur-Michałek; Marcin Ruciński; Mateusz Sowiński; Paulina Pietras; Marta Leśniczak-Staszak; Witold Szaflarski; Mark Isalan; Michal Mielcarek
Journal:  Cells       Date:  2022-05-18       Impact factor: 7.666

3.  Regulation of Melanocortin-3 and -4 Receptors by Isoforms of Melanocortin-2 Receptor Accessory Protein 1 and 2.

Authors:  Ren-Lei Ji; Ya-Xiong Tao
Journal:  Biomolecules       Date:  2022-02-02

4.  Contribution of Whole-Genome Sequencing and Transcript Analysis to Decipher Retinal Diseases Associated with MFSD8 Variants.

Authors:  Anaïs F Poncet; Olivier Grunewald; Veronika Vaclavik; Isabelle Meunier; Isabelle Drumare; Valérie Pelletier; Béatrice Bocquet; Margarita G Todorova; Anne-Gaëlle Le Moing; Aurore Devos; Daniel F Schorderet; Florence Jobic; Sabine Defoort-Dhellemmes; Hélène Dollfus; Vasily M Smirnov; Claire-Marie Dhaenens
Journal:  Int J Mol Sci       Date:  2022-04-13       Impact factor: 6.208

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.