Literature DB >> 27867341

Disorders of Transcriptional Regulation: An Emerging Category of Multiple Malformation Syndromes.

Kosuke Izumi1.   

Abstract

Some genetic disorders caused by mutations in genes encoding components of the transcriptional machinery as well as proteins involved in epigenetic modification of the genome share many overlapping features, such as facial dysmorphisms, growth problems and developmental delay/intellectual disability. As a basis for some shared phenotypic characteristics in these syndromes, a similar transcriptome disturbance, characterized by global transcriptional dysregulation, is believed to play a major role. In this review article, a general overview of gene transcription is provided, and the current knowledge of the mechanisms underlying some disorders of transcriptional regulation, such as Rubinstein- Taybi, Coffin-Siris, Cornelia de Lange, and CHOPS syndromes, are discussed.

Entities:  

Keywords:  Chromatin remodeling; Malformation syndromes; Transcriptional regulation

Year:  2016        PMID: 27867341      PMCID: PMC5109993          DOI: 10.1159/000448747

Source DB:  PubMed          Journal:  Mol Syndromol        ISSN: 1661-8769


  70 in total

1.  Selective anchoring of TFIID to nucleosomes by trimethylation of histone H3 lysine 4.

Authors:  Michiel Vermeulen; Klaas W Mulder; Sergei Denissov; W W M Pim Pijnappel; Frederik M A van Schaik; Radhika A Varier; Marijke P A Baltissen; Henk G Stunnenberg; Matthias Mann; H Th Marc Timmers
Journal:  Cell       Date:  2007-09-20       Impact factor: 41.582

2.  De novo loss-of-function mutations in X-linked SMC1A cause severe ID and therapy-resistant epilepsy in females: expanding the phenotypic spectrum.

Authors:  S Jansen; T Kleefstra; M H Willemsen; P de Vries; R Pfundt; J Y Hehir-Kwa; C Gilissen; J A Veltman; B B A de Vries; L E L M Vissers
Journal:  Clin Genet       Date:  2016-02-14       Impact factor: 4.438

3.  A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndrome.

Authors:  Hiba Risheg; John M Graham; Robin D Clark; R Curtis Rogers; John M Opitz; John B Moeschler; Andreas P Peiffer; Melanie May; Sumy M Joseph; Julie R Jones; Roger E Stevenson; Charles E Schwartz; Michael J Friez
Journal:  Nat Genet       Date:  2007-03-04       Impact factor: 38.330

4.  Mutations in ANKRD11 cause KBG syndrome, characterized by intellectual disability, skeletal malformations, and macrodontia.

Authors:  Asli Sirmaci; Michail Spiliopoulos; Francesco Brancati; Eric Powell; Duygu Duman; Alex Abrams; Guney Bademci; Emanuele Agolini; Shengru Guo; Berrin Konuk; Asli Kavaz; Susan Blanton; Maria Christina Digilio; Bruno Dallapiccola; Juan Young; Stephan Zuchner; Mustafa Tekin
Journal:  Am J Hum Genet       Date:  2011-07-21       Impact factor: 11.025

Review 5.  Mechanisms of cohesin-mediated gene regulation and lessons learned from cohesinopathies.

Authors:  Alexander R Ball; Yen-Yun Chen; Kyoko Yokomori
Journal:  Biochim Biophys Acta       Date:  2013-11-22

6.  De novo heterozygous mutations in SMC3 cause a range of Cornelia de Lange syndrome-overlapping phenotypes.

Authors:  María Concepción Gil-Rodríguez; Matthew A Deardorff; Morad Ansari; Christopher A Tan; Ilaria Parenti; Carolina Baquero-Montoya; Lilian B Ousager; Beatriz Puisac; María Hernández-Marcos; María Esperanza Teresa-Rodrigo; Iñigo Marcos-Alcalde; Jan-Jaap Wesselink; Silvia Lusa-Bernal; Emilia K Bijlsma; Diana Braunholz; Inés Bueno-Martinez; Dinah Clark; Nicola S Cooper; Cynthia J Curry; Richard Fisher; Alan Fryer; Jaya Ganesh; Cristina Gervasini; Gabriele Gillessen-Kaesbach; Yiran Guo; Hakon Hakonarson; Robert J Hopkin; Maninder Kaur; Brendan J Keating; María Kibaek; Esther Kinning; Tjitske Kleefstra; Antonie D Kline; Ekaterina Kuchinskaya; Lidia Larizza; Yun R Li; Xuanzhu Liu; Milena Mariani; Jonathan D Picker; Ángeles Pié; Jelena Pozojevic; Ethel Queralt; Julie Richer; Elizabeth Roeder; Anubha Sinha; Richard H Scott; Joyce So; Katherine A Wusik; Louise Wilson; Jianguo Zhang; Paulino Gómez-Puertas; César H Casale; Lena Ström; Angelo Selicorni; Feliciano J Ramos; Laird G Jackson; Ian D Krantz; Soma Das; Raoul C M Hennekam; Frank J Kaiser; David R FitzPatrick; Juan Pié
Journal:  Hum Mutat       Date:  2015-03-17       Impact factor: 4.878

7.  Nipbl and mediator cooperatively regulate gene expression to control limb development.

Authors:  Akihiko Muto; Shingo Ikeda; Martha E Lopez-Burks; Yutaka Kikuchi; Anne L Calof; Arthur D Lander; Thomas F Schilling
Journal:  PLoS Genet       Date:  2014-09-25       Impact factor: 5.917

8.  Genome-Wide Transcriptional Regulation Mediated by Biochemically Distinct SWI/SNF Complexes.

Authors:  Jesse R Raab; Samuel Resnick; Terry Magnuson
Journal:  PLoS Genet       Date:  2015-12-30       Impact factor: 5.917

9.  NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndrome.

Authors:  Emma T Tonkin; Tzu-Jou Wang; Steven Lisgo; Michael J Bamshad; Tom Strachan
Journal:  Nat Genet       Date:  2004-05-16       Impact factor: 38.330

10.  HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycle.

Authors:  Matthew A Deardorff; Masashige Bando; Ryuichiro Nakato; Erwan Watrin; Takehiko Itoh; Masashi Minamino; Katsuya Saitoh; Makiko Komata; Yuki Katou; Dinah Clark; Kathryn E Cole; Elfride De Baere; Christophe Decroos; Nataliya Di Donato; Sarah Ernst; Lauren J Francey; Yolanda Gyftodimou; Kyotaro Hirashima; Melanie Hullings; Yuuichi Ishikawa; Christian Jaulin; Maninder Kaur; Tohru Kiyono; Patrick M Lombardi; Laura Magnaghi-Jaulin; Geert R Mortier; Naohito Nozaki; Michael B Petersen; Hiroyuki Seimiya; Victoria M Siu; Yutaka Suzuki; Kentaro Takagaki; Jonathan J Wilde; Patrick J Willems; Claude Prigent; Gabriele Gillessen-Kaesbach; David W Christianson; Frank J Kaiser; Laird G Jackson; Toru Hirota; Ian D Krantz; Katsuhiko Shirahige
Journal:  Nature       Date:  2012-09-13       Impact factor: 49.962

View more
  15 in total

1.  Comprehensive genetic analysis of 57 families with clinically suspected Cornelia de Lange syndrome.

Authors:  Hiromi Aoi; Takeshi Mizuguchi; José Ricard Ceroni; Veronica Eun Hue Kim; Isabel Furquim; Rachel S Honjo; Takuma Iwaki; Toshifumi Suzuki; Futoshi Sekiguchi; Yuri Uchiyama; Yoshiteru Azuma; Kohei Hamanaka; Eriko Koshimizu; Satoko Miyatake; Satomi Mitsuhashi; Atsushi Takata; Noriko Miyake; Satoru Takeda; Atsuo Itakura; Débora R Bertola; Chong Ae Kim; Naomichi Matsumoto
Journal:  J Hum Genet       Date:  2019-07-23       Impact factor: 3.172

2.  ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder.

Authors:  Raphael Carapito; Ekaterina L Ivanova; Aurore Morlon; Linyan Meng; Anne Molitor; Eva Erdmann; Bruno Kieffer; Angélique Pichot; Lydie Naegely; Aline Kolmer; Nicodème Paul; Antoine Hanauer; Frédéric Tran Mau-Them; Nolwenn Jean-Marçais; Susan M Hiatt; Gregory M Cooper; Tatiana Tvrdik; Alison M Muir; Clémantine Dimartino; Maya Chopra; Jeanne Amiel; Christopher T Gordon; Fabien Dutreux; Aurore Garde; Christel Thauvin-Robinet; Xia Wang; Magalie S Leduc; Meredith Phillips; Heather P Crawford; Mary K Kukolich; David Hunt; Victoria Harrison; Mira Kharbanda; Robert Smigiel; Nina Gold; Christina Y Hung; David H Viskochil; Sarah L Dugan; Pinar Bayrak-Toydemir; Géraldine Joly-Helas; Anne-Marie Guerrot; Caroline Schluth-Bolard; Marlène Rio; Ingrid M Wentzensen; Kirsty McWalter; Rhonda E Schnur; Andrea M Lewis; Seema R Lalani; Noël Mensah-Bonsu; Jocelyn Céraline; Zijie Sun; Rafal Ploski; Carlos A Bacino; Heather C Mefford; Laurence Faivre; Olaf Bodamer; Jamel Chelly; Bertrand Isidor; Seiamak Bahram
Journal:  Am J Hum Genet       Date:  2019-01-10       Impact factor: 11.025

3.  WDR26 Haploinsufficiency Causes a Recognizable Syndrome of Intellectual Disability, Seizures, Abnormal Gait, and Distinctive Facial Features.

Authors:  Cara M Skraban; Constance F Wells; Preetha Markose; Megan T Cho; Addie I Nesbitt; P Y Billie Au; Amber Begtrup; John A Bernat; Lynne M Bird; Kajia Cao; Arjan P M de Brouwer; Elizabeth H Denenberg; Ganka Douglas; Kristin M Gibson; Katheryn Grand; Alice Goldenberg; A Micheil Innes; Jane Juusola; Marlies Kempers; Esther Kinning; David M Markie; Martina M Owens; Katelyn Payne; Richard Person; Rolph Pfundt; Amber Stocco; Claire L S Turner; Nienke E Verbeek; Laurence E Walsh; Taylor C Warner; Patricia G Wheeler; Dagmar Wieczorek; Alisha B Wilkens; Evelien Zonneveld-Huijssoon; Tjitske Kleefstra; Stephen P Robertson; Avni Santani; Koen L I van Gassen; Matthew A Deardorff
Journal:  Am J Hum Genet       Date:  2017-07-06       Impact factor: 11.025

4.  Mutations in chromatin regulators functionally link Cornelia de Lange syndrome and clinically overlapping phenotypes.

Authors:  Ilaria Parenti; María E Teresa-Rodrigo; Jelena Pozojevic; Sara Ruiz Gil; Ingrid Bader; Diana Braunholz; Nuria C Bramswig; Cristina Gervasini; Lidia Larizza; Lutz Pfeiffer; Ferda Ozkinay; Feliciano Ramos; Benedikt Reiz; Olaf Rittinger; Tim M Strom; Erwan Watrin; Kerstin Wendt; Dagmar Wieczorek; Bernd Wollnik; Carolina Baquero-Montoya; Juan Pié; Matthew A Deardorff; Gabriele Gillessen-Kaesbach; Frank J Kaiser
Journal:  Hum Genet       Date:  2017-01-24       Impact factor: 4.132

5.  Haploinsufficiency of the Sin3/HDAC corepressor complex member SIN3B causes a syndromic intellectual disability/autism spectrum disorder.

Authors:  Xenia Latypova; Marie Vincent; Alice Mollé; Oluwadamilare A Adebambo; Cynthia Fourgeux; Tahir N Khan; Alfonso Caro; Monica Rosello; Carmen Orellana; Dmitriy Niyazov; Damien Lederer; Marie Deprez; Yline Capri; Peter Kannu; Anne Claude Tabet; Jonathan Levy; Emmelien Aten; Nicolette den Hollander; Miranda Splitt; Jagdeep Walia; Ladonna L Immken; Pawel Stankiewicz; Kirsty McWalter; Sharon Suchy; Raymond J Louie; Shannon Bell; Roger E Stevenson; Justine Rousseau; Catherine Willem; Christelle Retiere; Xiang-Jiao Yang; Philippe M Campeau; Francisco Martinez; Jill A Rosenfeld; Cédric Le Caignec; Sébastien Küry; Sandra Mercier; Kamran Moradkhani; Solène Conrad; Thomas Besnard; Benjamin Cogné; Nicholas Katsanis; Stéphane Bézieau; Jeremie Poschmann; Erica E Davis; Bertrand Isidor
Journal:  Am J Hum Genet       Date:  2021-04-02       Impact factor: 11.025

6.  Disease-associated c-MYC downregulation in human disorders of transcriptional regulation.

Authors:  Maria M Pallotta; Maddalena Di Nardo; Patrizia Sarogni; Ian D Krantz; Antonio Musio
Journal:  Hum Mol Genet       Date:  2022-05-19       Impact factor: 5.121

7.  Structural analysis of histone deacetylase 8 mutants associated with Cornelia de Lange Syndrome spectrum disorders.

Authors:  Jeremy D Osko; Nicholas J Porter; Christophe Decroos; Matthew S Lee; Paris R Watson; Sarah E Raible; Ian D Krantz; Matthew A Deardorff; David W Christianson
Journal:  J Struct Biol       Date:  2020-12-11       Impact factor: 2.867

Review 8.  Cornelia de Lange syndrome: from molecular diagnosis to therapeutic approach.

Authors:  Patrizia Sarogni; Maria M Pallotta; Antonio Musio
Journal:  J Med Genet       Date:  2019-11-08       Impact factor: 6.318

9.  NIPBL+/- haploinsufficiency reveals a constellation of transcriptome disruptions in the pluripotent and cardiac states.

Authors:  Jason A Mills; Pamela S Herrera; Maninder Kaur; Lanfranco Leo; Deborah McEldrew; Jesus A Tintos-Hernandez; Ramakrishnan Rajagopalan; Alyssa Gagne; Zhe Zhang; Xilma R Ortiz-Gonzalez; Ian D Krantz
Journal:  Sci Rep       Date:  2018-01-18       Impact factor: 4.996

Review 10.  Genomic Diagnosis for Pediatric Disorders: Revolution and Evolution.

Authors:  Emilie Lalonde; Stefan Rentas; Fumin Lin; Matthew C Dulik; Cara M Skraban; Nancy B Spinner
Journal:  Front Pediatr       Date:  2020-07-08       Impact factor: 3.418

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.