Literature DB >> 25575569

Mutations in RAD21 disrupt regulation of APOB in patients with chronic intestinal pseudo-obstruction.

Elena Bonora1, Francesca Bianco1, Lina Cordeddu2, Michael Bamshad3, Ludmila Francescatto4, Dustin Dowless4, Vincenzo Stanghellini1, Rosanna F Cogliandro1, Greger Lindberg2, Zeynel Mungan5, Kivanc Cefle6, Tayfun Ozcelik7, Sukru Palanduz6, Sukru Ozturk6, Asuman Gedikbasi6, Alessandra Gori1, Tommaso Pippucci1, Claudio Graziano1, Umberto Volta1, Giacomo Caio1, Giovanni Barbara1, Mauro D'Amato2, Marco Seri1, Nicholas Katsanis4, Giovanni Romeo8, Roberto De Giorgio9.   

Abstract

BACKGROUND & AIMS: Chronic intestinal pseudo-obstruction (CIPO) is characterized by severe intestinal dysmotility that mimics a mechanical subocclusion with no evidence of gut obstruction. We searched for genetic variants associated with CIPO to increase our understanding of its pathogenesis and to identify potential biomarkers.
METHODS: We performed whole-exome sequencing of genomic DNA from patients with familial CIPO syndrome. Blood and lymphoblastoid cells were collected from patients and controls (individuals without CIPO); levels of messenger RNA (mRNA) and proteins were analyzed by quantitative reverse-transcription polymerase chain reaction, immunoblot, and mobility shift assays. Complementary DNAs were transfected into HEK293 cells. Expression of rad21 was suppressed in zebrafish embryos using a splice-blocking morpholino (rad21a). Gut tissues were collected and analyzed.
RESULTS: We identified a homozygous mutation (p.622, encodes Ala>Thr) in RAD21 in patients from a consanguineous family with CIPO. Expression of RUNX1, a target of RAD21, was reduced in cells from patients with CIPO compared with controls. In zebrafish, suppression of rad21a reduced expression of runx1; this phenotype was corrected by injection of human RAD21 mRNA, but not with the mRNA from the mutated p.622 allele. rad21a Morpholino zebrafish had delayed intestinal transit and greatly reduced numbers of enteric neurons, similar to patients with CIPO. This defect was greater in zebrafish with suppressed expression of ret and rad21, indicating their interaction in the regulation of gut neurogenesis. The promoter region of APOB bound RAD21 but not RAD21 p.622 Ala>Thr; expression of wild-type RAD21 in HEK293 cells repressed expression of APOB, compared with control vector. The gut-specific isoform of APOB (APOB48) is overexpressed in sera from patients with CIPO who carry the RAD21 mutation. APOB48 also is overexpressed in sporadic CIPO in sera and gut biopsy specimens.
CONCLUSIONS: Some patients with CIPO carry mutations in RAD21 that disrupt the ability of its product to regulate genes such as RUNX1 and APOB. Reduced expression of rad21 in zebrafish, and dysregulation of these target genes, disrupts intestinal transit and the development of enteric neurons.
Copyright © 2015 AGA Institute. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Animal Model; Genetic Analysis; Intestinal Motility; Sporadic and Familial Chronic Intestinal Pseudo-obstruction

Mesh:

Substances:

Year:  2015        PMID: 25575569      PMCID: PMC4375026          DOI: 10.1053/j.gastro.2014.12.034

Source DB:  PubMed          Journal:  Gastroenterology        ISSN: 0016-5085            Impact factor:   22.682


  42 in total

1.  A cohesin-RAD21 interactome.

Authors:  Anil K Panigrahi; Nenggang Zhang; Subhendu K Otta; Debananda Pati
Journal:  Biochem J       Date:  2012-03-15       Impact factor: 3.857

Review 2.  Therapeutic regulation of apoB100 metabolism in insulin resistance in vivo.

Authors:  Gerald F Watts; Esther M M Ooi; Dick C Chan
Journal:  Pharmacol Ther       Date:  2009-05-31       Impact factor: 12.310

3.  Microgavage of zebrafish larvae.

Authors:  Jordan L Cocchiaro; John F Rawls
Journal:  J Vis Exp       Date:  2013-02-20       Impact factor: 1.355

4.  The specific contributions of cohesin-SA1 to cohesion and gene expression: implications for cancer and development.

Authors:  Ana Cuadrado; Silvia Remeseiro; Gonzalo Gómez-López; David G Pisano; Ana Losada
Journal:  Cell Cycle       Date:  2012-06-15       Impact factor: 4.534

5.  Recurrent mutations in multiple components of the cohesin complex in myeloid neoplasms.

Authors:  Ayana Kon; Lee-Yung Shih; Masashi Minamino; Masashi Sanada; Yuichi Shiraishi; Yasunobu Nagata; Kenichi Yoshida; Yusuke Okuno; Masashige Bando; Ryuichiro Nakato; Shumpei Ishikawa; Aiko Sato-Otsubo; Genta Nagae; Aiko Nishimoto; Claudia Haferlach; Daniel Nowak; Yusuke Sato; Tamara Alpermann; Masao Nagasaki; Teppei Shimamura; Hiroko Tanaka; Kenichi Chiba; Ryo Yamamoto; Tomoyuki Yamaguchi; Makoto Otsu; Naoshi Obara; Mamiko Sakata-Yanagimoto; Tsuyoshi Nakamaki; Ken Ishiyama; Florian Nolte; Wolf-Karsten Hofmann; Shuichi Miyawaki; Shigeru Chiba; Hiraku Mori; Hiromitsu Nakauchi; H Phillip Koeffler; Hiroyuki Aburatani; Torsten Haferlach; Katsuhiko Shirahige; Satoru Miyano; Seishi Ogawa
Journal:  Nat Genet       Date:  2013-08-18       Impact factor: 38.330

6.  Apolipoprotein B is a new target of the GDNF/RET and ET-3/EDNRB signalling pathways.

Authors:  C Evangelisti; F Bianco; L M Pradella; A Puliti; A Goldoni; I Sbrana; M Rossi; M Vargiolu; M Seri; G Romeo; V Stanghellini; R de Giorgio; E Bonora
Journal:  Neurogastroenterol Motil       Date:  2012-08-16       Impact factor: 3.598

7.  RAD21 mutations cause a human cohesinopathy.

Authors:  Matthew A Deardorff; Jonathan J Wilde; Melanie Albrecht; Emma Dickinson; Stephanie Tennstedt; Diana Braunholz; Maren Mönnich; Yuqian Yan; Weizhen Xu; María Concepcion Gil-Rodríguez; Dinah Clark; Hakon Hakonarson; Sara Halbach; Laura Daniela Michelis; Abhinav Rampuria; Eva Rossier; Stephanie Spranger; Lionel Van Maldergem; Sally Ann Lynch; Gabriele Gillessen-Kaesbach; Hermann-Josef Lüdecke; Robert G Ramsay; Michael J McKay; Ian D Krantz; Huiling Xu; Julia A Horsfield; Frank J Kaiser
Journal:  Am J Hum Genet       Date:  2012-05-24       Impact factor: 11.025

8.  Cohesin and CTCF differentially regulate spatiotemporal runx1 expression during zebrafish development.

Authors:  Judith Marsman; Adam C O'Neill; Betty Rui-Yun Kao; Jenny M Rhodes; Michael Meier; Jisha Antony; Maren Mönnich; Julia A Horsfield
Journal:  Biochim Biophys Acta       Date:  2013-12-07

9.  Two novel RAD21 mutations in patients with mild Cornelia de Lange syndrome-like presentation and report of the first familial case.

Authors:  Agata Minor; Marwan Shinawi; Jacob S Hogue; Marisa Vineyard; Damara R Hamlin; Christopher Tan; Kirsten Donato; Latrice Wysinger; Shaun Botes; Soma Das; Daniela Del Gaudio
Journal:  Gene       Date:  2013-12-27       Impact factor: 3.688

10.  Rad21-cohesin haploinsufficiency impedes DNA repair and enhances gastrointestinal radiosensitivity in mice.

Authors:  Huiling Xu; Kuhendra Balakrishnan; Jordane Malaterre; Matthew Beasley; Yuqian Yan; Jeroen Essers; Esther Appeldoorn; Jonathan M Tomaszewski; Jonathan M Thomaszewski; Melisa Vazquez; Sandra Verschoor; Martin F Lavin; Ivan Bertoncello; Ivan Bertonchello; Robert G Ramsay; Michael J McKay
Journal:  PLoS One       Date:  2010-08-12       Impact factor: 3.240

View more
  22 in total

Review 1.  Advances in Enteric Neurobiology: The "Brain" in the Gut in Health and Disease.

Authors:  Subhash Kulkarni; Julia Ganz; James Bayrer; Laren Becker; Milena Bogunovic; Meenakshi Rao
Journal:  J Neurosci       Date:  2018-10-31       Impact factor: 6.167

2.  Diagnosis of Chronic Intestinal Pseudo-obstruction and Megacystis by Sequencing the ACTG2 Gene.

Authors:  Aubrey Milunsky; Clinton Baldwin; Xiaoying Zhang; Daniel Primack; Adrian Curnow; Jeff Milunsky
Journal:  J Pediatr Gastroenterol Nutr       Date:  2017-10       Impact factor: 2.839

3.  Expression of RAD21 immunoreactivity in myenteric neurons of the human and mouse small intestine.

Authors:  F Bianco; S T Eisenman; M G Colmenares Aguilar; E Bonora; P Clavenzani; D R Linden; R De Giorgio; G Farrugia; S J Gibbons
Journal:  Neurogastroenterol Motil       Date:  2018-08-01       Impact factor: 3.598

4.  Loss-of-Function Mutations in UNC45A Cause a Syndrome Associating Cholestasis, Diarrhea, Impaired Hearing, and Bone Fragility.

Authors:  Clothilde Esteve; Ludmila Francescatto; Perciliz L Tan; Aurélie Bourchany; Cécile De Leusse; Evelyne Marinier; Arnaud Blanchard; Patrice Bourgeois; Céline Brochier-Armanet; Ange-Line Bruel; Arnauld Delarue; Yannis Duffourd; Emmanuelle Ecochard-Dugelay; Géraldine Hery; Frédéric Huet; Philippe Gauchez; Emmanuel Gonzales; Catherine Guettier-Bouttier; Mina Komuta; Caroline Lacoste; Raphaelle Maudinas; Karin Mazodier; Yves Rimet; Jean-Baptiste Rivière; Bertrand Roquelaure; Sabine Sigaudy; Xavier Stephenne; Christel Thauvin-Robinet; Julien Thevenon; Jacques Sarles; Nicolas Levy; Catherine Badens; Olivier Goulet; Jean-Pierre Hugot; Nicholas Katsanis; Laurence Faivre; Alexandre Fabre
Journal:  Am J Hum Genet       Date:  2018-02-08       Impact factor: 11.025

Review 5.  Pediatric Intestinal Pseudo-obstruction in the Era of Genetic Sequencing.

Authors:  Heidi E Gamboa; Manu Sood
Journal:  Curr Gastroenterol Rep       Date:  2019-12-17

Review 6.  [Motility disorders of the small intestine].

Authors:  J Keller; P Layer
Journal:  Internist (Berl)       Date:  2015-06       Impact factor: 0.743

Review 7.  Cohesin subunit RAD21: From biology to disease.

Authors:  Haizi Cheng; Nenggang Zhang; Debananda Pati
Journal:  Gene       Date:  2020-07-17       Impact factor: 3.688

8.  The expanding phenotypes of cohesinopathies: one ring to rule them all!

Authors:  Jessica Piché; Patrick Piet Van Vliet; Michel Pucéat; Gregor Andelfinger
Journal:  Cell Cycle       Date:  2019-09-13       Impact factor: 4.534

9.  Dysregulation of the NRG1/ERBB pathway causes a developmental disorder with gastrointestinal dysmotility in humans.

Authors:  Thuy-Linh Le; Louise Galmiche; Jonathan Levy; Pim Suwannarat; Debby Mei Hellebrekers; Khomgrit Morarach; Franck Boismoreau; Tom Ej Theunissen; Mathilde Lefebvre; Anna Pelet; Jelena Martinovic; Antoinette Gelot; Fabien Guimiot; Amanda Calleroz; Cyril Gitiaux; Marie Hully; Olivier Goulet; Christophe Chardot; Severine Drunat; Yline Capri; Christine Bole-Feysot; Patrick Nitschké; Sandra Whalen; Linda Mouthon; Holly E Babcock; Robert Hofstra; Irenaeus Fm de Coo; Anne-Claude Tabet; Thierry J Molina; Boris Keren; Alice Brooks; Hubert Jm Smeets; Ulrika Marklund; Christopher T Gordon; Stanislas Lyonnet; Jeanne Amiel; Nadège Bondurand
Journal:  J Clin Invest       Date:  2021-03-15       Impact factor: 14.808

10.  A Novel Mutation in Nucleoporin 35 Causes Murine Degenerative Colonic Smooth Muscle Myopathy.

Authors:  Ian A Parish; Lincon A Stamp; Ayla May D Lorenzo; Suzanne M Fowler; Yovina Sontani; Lisa A Miosge; Debbie R Howard; Christopher C Goodnow; Heather M Young; John B Furness
Journal:  Am J Pathol       Date:  2016-07-16       Impact factor: 4.307

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.