Literature DB >> 27226544

Exon Skipping in the RET Gene Encodes Novel Isoforms That Differentially Regulate RET Protein Signal Transduction.

Nicole A Gabreski1, Janki K Vaghasia2, Silvia S Novakova2, Neil Q McDonald3, Brian A Pierchala4.   

Abstract

Rearranged during transfection (RET), a receptor tyrosine kinase that is activated by the glial cell line-derived neurotrophic factor family ligands (GFLs), plays a crucial role in the development and function of the nervous system and additionally is required for kidney development and spermatogenesis. RET encodes a transmembrane receptor that is 20 exons long and produces two known protein isoforms differing in C-terminal amino acid composition, referred to as RET9 and RET51. Studies of human pheochromocytomas identified two additional novel transcripts involving the skipping of exon 3 or exons 3, 4, and 5 and are referred to as RET(Δ) (E3) and RET(Δ) (E345), respectively. Here we report the presence of Ret(Δ) (E3) and Ret(Δ) (E345) in zebrafish, mice, and rats and show that these transcripts are dynamically expressed throughout development of the CNS, peripheral nervous system, and kidneys. We further explore the biochemical properties of these isoforms, demonstrating that, like full-length RET, RET(ΔE3) and RET(ΔE345) are trafficked to the cell surface, interact with all four GFRα co-receptors, and have the ability to heterodimerize with full-length RET. Signaling experiments indicate that RET(ΔE3) is phosphorylated in a similar manner to full-length RET. RET(ΔE345), in contrast, displays higher baseline autophosphorylation, specifically on the catalytic tyrosine, Tyr(905), and also on one of the most important signaling residues, Tyr(1062) These data provide the first evidence for a physiologic role of these isoforms in RET pathway function.
© 2016 by The American Society for Biochemistry and Molecular Biology, Inc.

Entities:  

Keywords:  alternative splicing; cell signaling; neurotrophic factor; receptor tyrosine kinase; signal transduction

Mesh:

Substances:

Year:  2016        PMID: 27226544      PMCID: PMC4965573          DOI: 10.1074/jbc.M115.709675

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  58 in total

Review 1.  GDNF family neurotrophic factor signaling: four masters, one servant?

Authors:  M S Airaksinen; A Titievsky; M Saarma
Journal:  Mol Cell Neurosci       Date:  1999-05       Impact factor: 4.314

2.  RET alternate splicing influences the interaction of activated RET with the SH2 and PTB domains of Shc, and the SH2 domain of Grb2.

Authors:  M J Lorenzo; G D Gish; C Houghton; T J Stonehouse; T Pawson; B A Ponder; D P Smith
Journal:  Oncogene       Date:  1997-02-20       Impact factor: 9.867

3.  Signaling complexes and protein-protein interactions involved in the activation of the Ras and phosphatidylinositol 3-kinase pathways by the c-Ret receptor tyrosine kinase.

Authors:  V Besset; R P Scott; C F Ibáñez
Journal:  J Biol Chem       Date:  2000-12-15       Impact factor: 5.157

Review 4.  RET revisited: expanding the oncogenic portfolio.

Authors:  Lois M Mulligan
Journal:  Nat Rev Cancer       Date:  2014-03       Impact factor: 60.716

5.  Characterization of RET proto-oncogene 3' splicing variants and polyadenylation sites: a novel C-terminus for RET.

Authors:  S M Myers; C Eng; B A Ponder; L M Mulligan
Journal:  Oncogene       Date:  1995-11-16       Impact factor: 9.867

6.  Characterization of intracellular signals via tyrosine 1062 in RET activated by glial cell line-derived neurotrophic factor.

Authors:  H Hayashi; M Ichihara; T Iwashita; H Murakami; Y Shimono; K Kawai; K Kurokawa; Y Murakumo; T Imai; H Funahashi; A Nakao; M Takahashi
Journal:  Oncogene       Date:  2000-09-14       Impact factor: 9.867

Review 7.  Targeting the RET pathway in thyroid cancer.

Authors:  Samuel A Wells; Massimo Santoro
Journal:  Clin Cancer Res       Date:  2009-11-24       Impact factor: 12.531

8.  The Ret receptor protein tyrosine kinase associates with the SH2-containing adapter protein Grb10.

Authors:  A Pandey; H Duan; P P Di Fiore; V M Dixit
Journal:  J Biol Chem       Date:  1995-09-15       Impact factor: 5.157

9.  The neurotrophic effects of glial cell line-derived neurotrophic factor on spinal motoneurons are restricted to fusimotor subtypes.

Authors:  Thomas W Gould; Shigenobu Yonemura; Ronald W Oppenheim; Shiho Ohmori; Hideki Enomoto
Journal:  J Neurosci       Date:  2008-02-27       Impact factor: 6.167

10.  Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret.

Authors:  A Schuchardt; V D'Agati; L Larsson-Blomberg; F Costantini; V Pachnis
Journal:  Nature       Date:  1994-01-27       Impact factor: 49.962

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  3 in total

1.  Biosystems Study of the Molecular Networks Underlying Hippocampal Aging Progression and Anti-aging Treatment in Mice.

Authors:  Jiao Wang; Qian Li; Yanyan Kong; Fangfang Zhou; Jie Li; Weihao Li; Kai Wang; Ting Wu; Yihui Guan; Jiang Xie; Tieqiao Wen
Journal:  Front Aging Neurosci       Date:  2017-12-06       Impact factor: 5.750

2.  Event Analysis: Using Transcript Events To Improve Estimates of Abundance in RNA-seq Data.

Authors:  Jeremy R B Newman; Patrick Concannon; Manuel Tardaguila; Ana Conesa; Lauren M McIntyre
Journal:  G3 (Bethesda)       Date:  2018-08-30       Impact factor: 3.154

3.  Artemin and an Artemin-Derived Peptide, Artefin, Induce Neuronal Survival, and Differentiation Through Ret and NCAM.

Authors:  Mirolyuba Ilieva; Janne Nielsen; Irina Korshunova; Kamil Gotfryd; Elisabeth Bock; Stanislava Pankratova; Tanja Maria Michel
Journal:  Front Mol Neurosci       Date:  2019-02-22       Impact factor: 5.639

  3 in total

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