Back to Search Start Over

INTS13 variants causing a recessive developmental ciliopathy disrupt assembly of the Integrator complex

Authors :
Lauren G. Mascibroda
Mohammad Shboul
Nathan D. Elrod
Laurence Colleaux
Hanan Hamamy
Kai-Lieh Huang
Natoya Peart
Moirangthem Kiran Singh
Hane Lee
Barry Merriman
Jeanne N. Jodoin
Poojitha Sitaram
Laura A. Lee
Raja Fathalla
Baeth Al-Rawashdeh
Osama Ababneh
Mohammad El-Khateeb
Nathalie Escande-Beillard
Stanley F. Nelson
Yixuan Wu
Liang Tong
Linda J. Kenney
Sudipto Roy
William K. Russell
Jeanne Amiel
Bruno Reversade
Eric J. Wagner
Source :
Nature Communications, Vol 13, Iss 1, Pp 1-17 (2022)
Publication Year :
2022
Publisher :
Nature Portfolio, 2022.

Abstract

The integrator complex is required for the synthesis of protein coding and non-coding RNA and contains the protein INTS13. Here, the authors find germline mutations in INTS13 in two families with oral facial digital syndrome and show that the mutation affects the c-terminal domain of the protein and disrupts cilliogenesis.

Subjects

Subjects :
Science

Details

Language :
English
ISSN :
20411723
Volume :
13
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
edsdoj.35883c108c1d4e72ba468a3fd1444767
Document Type :
article
Full Text :
https://doi.org/10.1038/s41467-022-33547-8