Literature DB >> 29363216

Diagnostic yield of a targeted gene panel in primary ciliary dyskinesia patients.

Tamara Paff1,2,3, Irsan E Kooi3, Youssef Moutaouakil3, Elise Riesebos3, Erik A Sistermans3, Hans J M A Daniels1, Janneke M M Weiss3, Hans H W M Niessen4, Eric G Haarman2, Gerard Pals3, Dimitra Micha3.   

Abstract

We aimed to determine the diagnostic yield of a targeted-exome panel in a cohort of 74 Dutch primary ciliary dyskinesia (PCD) patients. The panel consisted of 26 PCD-related and 284 candidate genes. To prioritize PCD candidate genes, we investigated the transcriptome of human airway cells of 12 healthy volunteers during in vitro ciliogenesis and hypothesized that PCD-related genes show significant upregulation. We compared gene expression in epithelial precursor cells grown as collagen monolayer and ciliated cells grown in suspension by RNA sequencing. All genes reported as PCD causative, except NME8, showed significant upregulation during in vitro ciliogenesis. We observed 67.6% diagnostic yield when testing the targeted-exome panel in our cohort. There was relatively high percentage of DNAI and HYDIN mutations compared to other countries. The latter may be due to our solution for the problem of the confounding HYDIN2 pseudogene. Candidate genes included two recently published PCD-related genes DNAJB13 and PIH1D3; identification of the latter was a direct result of this study. In conclusion, we demonstrate 67.6% diagnostic yield by targeted exome sequencing in a Dutch PCD population and present a highly sensitive and moderately specific approach for identification of PCD-related genes, based on significant upregulation during in vitro ciliogenesis.
© 2018 Wiley Periodicals, Inc.

Entities:  

Keywords:  RNA sequencing; ciliogenesis; primary ciliary dyskinesia; targeted exome sequencing

Mesh:

Year:  2018        PMID: 29363216     DOI: 10.1002/humu.23403

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  9 in total

1.  A Novel Homozygous Nonsense HYDIN Gene Mutation p.(Arg951*) in Primary Ciliary Dyskinesia.

Authors:  Antony Terance Benjamin; Ram Ganesh; Balan Louis Gaspar; Jane Lucas; Claire Jackson; Marie Legendre; Rahma Mani; Estelle Escudier
Journal:  Indian J Pediatr       Date:  2019-05-14       Impact factor: 1.967

2.  Novel compound heterozygous DNAAF2 mutations cause primary ciliary dyskinesia in a Han Chinese family.

Authors:  Minghan Sun; Yi Zhang; Yi Wang; Hao Tan; Hailian Wang; Tiantian Lei; Xiaojie Li; Xiaojian Zhang; Wen Xiong; Ke Dou; Yongxin Ma
Journal:  J Assist Reprod Genet       Date:  2020-07-07       Impact factor: 3.412

3.  Identification of Two Novel DNAAF2 Variants in Two Consanguineous Families with Primary Ciliary Dyskinesia.

Authors:  Chenyang Lu; Danhui Yang; Cheng Lei; Rongchun Wang; Ting Guo; Hong Luo
Journal:  Pharmgenomics Pers Med       Date:  2021-11-10

4.  Recessive DNAH9 Loss-of-Function Mutations Cause Laterality Defects and Subtle Respiratory Ciliary-Beating Defects.

Authors:  Niki T Loges; Dinu Antony; Ales Maver; Matthew A Deardorff; Elif Yýlmaz Güleç; Alper Gezdirici; Tabea Nöthe-Menchen; Inga M Höben; Lena Jelten; Diana Frank; Claudius Werner; Johannes Tebbe; Kaman Wu; Elizabeth Goldmuntz; Goran Čuturilo; Bryan Krock; Alyssa Ritter; Rim Hjeij; Zeineb Bakey; Petra Pennekamp; Bernd Dworniczak; Han Brunner; Borut Peterlin; Cansaran Tanidir; Heike Olbrich; Heymut Omran; Miriam Schmidts
Journal:  Am J Hum Genet       Date:  2018-11-21       Impact factor: 11.025

5.  Spectrum of Genetic Variants in a Cohort of 37 Laterality Defect Cases.

Authors:  Dinu Antony; Elif Gulec Yilmaz; Alper Gezdirici; Lennart Slagter; Zeineb Bakey; Helen Bornaun; Ibrahim Cansaran Tanidir; Tran Van Dinh; Han G Brunner; Peter Walentek; Sebastian J Arnold; Rolf Backofen; Miriam Schmidts
Journal:  Front Genet       Date:  2022-04-13       Impact factor: 4.772

Review 6.  Chronic airway disease in primary ciliary dyskinesia-spiced with geno-phenotype associations.

Authors:  Kim G Nielsen; Mathias G Holgersen; Suzanne Crowley; June K Marthin
Journal:  Am J Med Genet C Semin Med Genet       Date:  2022-03-29       Impact factor: 3.359

7.  Clinical characteristics and genetic spectrum of 26 individuals of Chinese origin with primary ciliary dyskinesia.

Authors:  Xinyue Zhao; Chun Bian; Keqiang Liu; Wenshuai Xu; Yaping Liu; Xinlun Tian; Jing Bai; Kai-Feng Xu; Xue Zhang
Journal:  Orphanet J Rare Dis       Date:  2021-07-01       Impact factor: 4.123

8.  Identification of Pathogenic Mutations and Investigation of the NOTCH Pathway Activation in Kartagener Syndrome.

Authors:  Yongjian Yue; Qijun Huang; Peng Zhu; Pan Zhao; Xinjuan Tan; Shengguo Liu; Shulin Li; Xuemei Han; Linling Cheng; Bo Li; Yingyun Fu
Journal:  Front Genet       Date:  2019-08-22       Impact factor: 4.599

Review 9.  Childhood rare lung disease in the 21st century: "-omics" technology advances accelerating discovery.

Authors:  Timothy J Vece; Jennifer A Wambach; James S Hagood
Journal:  Pediatr Pulmonol       Date:  2020-07
  9 in total

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