Your browser doesn't support javascript.
loading
INTS13 variants causing a recessive developmental ciliopathy disrupt assembly of the Integrator complex.
Mascibroda, Lauren G; Shboul, Mohammad; Elrod, Nathan D; Colleaux, Laurence; Hamamy, Hanan; Huang, Kai-Lieh; Peart, Natoya; Singh, Moirangthem Kiran; Lee, Hane; Merriman, Barry; Jodoin, Jeanne N; Sitaram, Poojitha; Lee, Laura A; Fathalla, Raja; Al-Rawashdeh, Baeth; Ababneh, Osama; El-Khateeb, Mohammad; Escande-Beillard, Nathalie; Nelson, Stanley F; Wu, Yixuan; Tong, Liang; Kenney, Linda J; Roy, Sudipto; Russell, William K; Amiel, Jeanne; Reversade, Bruno; Wagner, Eric J.
Afiliação
  • Mascibroda LG; Department of Biochemistry and Molecular Biology, The University of Texas Medical Branch at Galveston, Galveston, TX, 77550, USA.
  • Shboul M; Department of Medical Laboratory Sciences, Jordan University of Science and Technology, Irbid, Jordan.
  • Elrod ND; Department of Biochemistry and Molecular Biology, The University of Texas Medical Branch at Galveston, Galveston, TX, 77550, USA.
  • Colleaux L; Inserm UMR 1163, Institut Imagine, 24 Boulevard du Montparnasse, 75015, Paris, France.
  • Hamamy H; Department of Genetic Medicine and Development, University Hospital, Geneva, Switzerland.
  • Huang KL; Department of Biochemistry and Molecular Biology, The University of Texas Medical Branch at Galveston, Galveston, TX, 77550, USA.
  • Peart N; Department of Biochemistry and Biophysics, University of Rochester School of Medicine Dentistry, Rochester, NY, 14642, USA.
  • Singh MK; Center for RNA Biology, University of Rochester School of Medicine Dentistry, Rochester, NY, 14642, USA.
  • Lee H; Department of Biochemistry and Molecular Biology, The University of Texas Medical Branch at Galveston, Galveston, TX, 77550, USA.
  • Merriman B; Department of Biochemistry and Molecular Biology, The University of Texas Medical Branch at Galveston, Galveston, TX, 77550, USA.
  • Jodoin JN; Department of Pathology and Laboratory Medicine, Department of Human Genetics, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, 90095, USA.
  • Sitaram P; 3billion, Inc., Seoul, South Korea.
  • Lee LA; Department of Pathology and Laboratory Medicine, Department of Human Genetics, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, 90095, USA.
  • Fathalla R; Department of Cell and Developmental Biology, Vanderbilt University Medical Center, Nashville, TN, 37232, USA.
  • Al-Rawashdeh B; Department of Cell and Developmental Biology, Vanderbilt University Medical Center, Nashville, TN, 37232, USA.
  • Ababneh O; Department of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, TN, 37232, USA.
  • El-Khateeb M; National Center for Diabetes, Endocrinology and Genetics, Amman, Jordan.
  • Escande-Beillard N; Faculty of Medicine, Hospital of the University of Jordan, University of Jordan, Amman, Jordan.
  • Nelson SF; Faculty of Medicine, Hospital of the University of Jordan, University of Jordan, Amman, Jordan.
  • Wu Y; National Center for Diabetes, Endocrinology and Genetics, Amman, Jordan.
  • Tong L; Department of Medical Genetics, KOÇ University, Istanbul, Turkey.
  • Kenney LJ; Institute of Molecular and Cell Biology, A*STAR, Singapore, Singapore.
  • Roy S; Department of Pathology and Laboratory Medicine, Department of Human Genetics, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, 90095, USA.
  • Russell WK; Department of Biological Sciences, Columbia University, New York, NY, 10027, USA.
  • Amiel J; Department of Biological Sciences, Columbia University, New York, NY, 10027, USA.
  • Reversade B; Department of Biochemistry and Molecular Biology, The University of Texas Medical Branch at Galveston, Galveston, TX, 77550, USA.
  • Wagner EJ; Institute of Molecular and Cell Biology, A*STAR, Singapore, Singapore.
Nat Commun ; 13(1): 6054, 2022 10 13.
Article em En | MEDLINE | ID: mdl-36229431
Oral-facial-digital (OFD) syndromes are a heterogeneous group of congenital disorders characterized by malformations of the face and oral cavity, and digit anomalies. Mutations within 12 cilia-related genes have been identified that cause several types of OFD, suggesting that OFDs constitute a subgroup of developmental ciliopathies. Through homozygosity mapping and exome sequencing of two families with variable OFD type 2, we identified distinct germline variants in INTS13, a subunit of the Integrator complex. This multiprotein complex associates with RNA Polymerase II and cleaves nascent RNA to modulate gene expression. We determined that INTS13 utilizes its C-terminus to bind the Integrator cleavage module, which is disrupted by the identified germline variants p.S652L and p.K668Nfs*9. Depletion of INTS13 disrupts ciliogenesis in human cultured cells and causes dysregulation of a broad collection of ciliary genes. Accordingly, its knockdown in Xenopus embryos leads to motile cilia anomalies. Altogether, we show that mutations in INTS13 cause an autosomal recessive ciliopathy, which reveals key interactions between components of the Integrator complex.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndromes Orofaciodigitais / Proteínas de Transporte / Proteínas de Ciclo Celular / Ciliopatias Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndromes Orofaciodigitais / Proteínas de Transporte / Proteínas de Ciclo Celular / Ciliopatias Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article