Literature DB >> 34785929

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

Chenyang Lu1,2,3, Danhui Yang1,2,3, Cheng Lei1,2,3, Rongchun Wang1,2,3, Ting Guo1,2,3, Hong Luo1,2,3.   

Abstract

BACKGROUND: Dynein axonemal assembly factor 2 (DNAAF2) is involved in the early preassembly of dynein in the cytoplasm, which is essential for motile cilia function. Primary ciliary dyskinesia (PCD) associated with DNAAF2 variants has rarely been reported in females with infertility. Moreover, there is no report linking DNAAF2 to scoliosis in human.
MATERIALS AND METHODS: We recruited patients from two consanguineous families with a clinical diagnosis of PCD and collected their clinical history, laboratory tests, and radiographic data. Sequencing and bioinformatics analysis were then performed. Immunofluorescence and high-speed microscope analysis were used to support the pathogenicity of the variant.
RESULTS: Proband 1, a 26-year-old female from family I, exhibited scoliosis, bronchiectasis, sinusitis, situs inversus, and infertility. We found a novel homozygous missense variant in DNAAF2, c.491T>C, p.(Leu164Pro) in this patient. Subsequent immunofluorescence indicated the absence of outer dynein arm and inner dynein arm of cilia, and high-speed microscopy analysis showed that the most of the cilia are static, which support the pathogenicity of this variant. Proband 2, a 53-year-old female, presented with bronchiectasis, sinusitis, and infertility. In this patient, a new homozygous frameshift variant DNAAF2, c.822del, p.(Ala275Profs*10) was identified. The disease-causing variants mentioned above are not included in the current authorized genetic databases.
CONCLUSION: Our findings expand the spectrum of DNAAF2 variants and link DNAAF2 to female infertility and likely scoliosis in patients with PCD.
© 2021 Lu et al.

Entities:  

Keywords:  DNAAF2; bronchiectasis; female infertility; primary ciliary dyskinesia; scoliosis; situs inversus

Year:  2021        PMID: 34785929      PMCID: PMC8591118          DOI: 10.2147/PGPM.S338981

Source DB:  PubMed          Journal:  Pharmgenomics Pers Med        ISSN: 1178-7066


  40 in total

1.  Genotype and phenotype evaluation of patients with primary ciliary dyskinesia: First results from Turkey.

Authors:  Nagehan Emiralioğlu; Ekim Z Taşkıran; Can Koşukcu; Elif Bilgiç; Pergin Atilla; Bengisu Kaya; Önder Günaydın; Ayşe Yüzbaşıoğlu; Gökçen Dilşa Tuğcu; Dilber Ademhan; Sanem Eryılmaz Polat; Mina Gharibzadeh Hızal; Ebru Yalçın; Deniz Doğru; Nural Kiper; Mehmet Alikaşifoğlu; Uğur Özçelik
Journal:  Pediatr Pulmonol       Date:  2019-11-25

Review 2.  The adult scoliosis.

Authors:  Max Aebi
Journal:  Eur Spine J       Date:  2005-11-18       Impact factor: 3.134

3.  A novel homozygous mutation in FGFR3 causes tall stature, severe lateral tibial deviation, scoliosis, hearing impairment, camptodactyly, and arachnodactyly.

Authors:  Periklis Makrythanasis; Samia Temtamy; Mona S Aglan; Ghada A Otaify; Hanan Hamamy; Stylianos E Antonarakis
Journal:  Hum Mutat       Date:  2014-06-28       Impact factor: 4.878

Review 4.  Motile ciliopathies.

Authors:  Julia Wallmeier; Kim G Nielsen; Claudia E Kuehni; Jane S Lucas; Margaret W Leigh; Maimoona A Zariwala; Heymut Omran
Journal:  Nat Rev Dis Primers       Date:  2020-09-17       Impact factor: 52.329

5.  Ciliary function and motor protein composition of human fallopian tubes.

Authors:  Johanna Raidt; Claudius Werner; Tabea Menchen; Gerard W Dougherty; Heike Olbrich; Niki T Loges; Ralf Schmitz; Petra Pennekamp; Heymut Omran
Journal:  Hum Reprod       Date:  2015-09-15       Impact factor: 6.918

Review 6.  Adolescent idiopathic scoliosis.

Authors:  Jack C Cheng; René M Castelein; Winnie C Chu; Aina J Danielsson; Matthew B Dobbs; Theodoros B Grivas; Christina A Gurnett; Keith D Luk; Alain Moreau; Peter O Newton; Ian A Stokes; Stuart L Weinstein; R Geoffrey Burwell
Journal:  Nat Rev Dis Primers       Date:  2015-09-24       Impact factor: 52.329

Review 7.  Primary Ciliary Dyskinesia: An Update on Clinical Aspects, Genetics, Diagnosis, and Future Treatment Strategies.

Authors:  Virginia Mirra; Claudius Werner; Francesca Santamaria
Journal:  Front Pediatr       Date:  2017-06-09       Impact factor: 3.418

8.  Identification of Elongated Primary Cilia with Impaired Mechanotransduction in Idiopathic Scoliosis Patients.

Authors:  Niaz Oliazadeh; Kristen F Gorman; Robert Eveleigh; Guillaume Bourque; Alain Moreau
Journal:  Sci Rep       Date:  2017-03-14       Impact factor: 4.379

9.  Ktu/PF13 is required for cytoplasmic pre-assembly of axonemal dyneins.

Authors:  Heymut Omran; Daisuke Kobayashi; Heike Olbrich; Tatsuya Tsukahara; Niki T Loges; Haruo Hagiwara; Qi Zhang; Gerard Leblond; Eileen O'Toole; Chikako Hara; Hideaki Mizuno; Hiroyuki Kawano; Manfred Fliegauf; Toshiki Yagi; Sumito Koshida; Atsushi Miyawaki; Hanswalter Zentgraf; Horst Seithe; Richard Reinhardt; Yoshinori Watanabe; Ritsu Kamiya; David R Mitchell; Hiroyuki Takeda
Journal:  Nature       Date:  2008-12-04       Impact factor: 49.962

10.  Tbx6 regulates left/right patterning in mouse embryos through effects on nodal cilia and perinodal signaling.

Authors:  Anna-Katerina Hadjantonakis; Elinor Pisano; Virginia E Papaioannou
Journal:  PLoS One       Date:  2008-06-25       Impact factor: 3.240

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  2 in total

Review 1.  Turning the Curve Into Straight: Phenogenetics of the Spine Morphology and Coordinate Maintenance in the Zebrafish.

Authors:  Carlos Muñoz-Montecinos; Adrián Romero; Vania Sepúlveda; María Ángela Vira; Karen Fehrmann-Cartes; Sylvain Marcellini; Felipe Aguilera; Teresa Caprile; Ricardo Fuentes
Journal:  Front Cell Dev Biol       Date:  2022-01-26

2.  Case Report: DNAAF4 Variants Cause Primary Ciliary Dyskinesia and Infertility in Two Han Chinese Families.

Authors:  Ting Guo; Chenyang Lu; Danhui Yang; Cheng Lei; Ying Liu; Yingjie Xu; Binyi Yang; Rongchun Wang; Hong Luo
Journal:  Front Genet       Date:  2022-07-12       Impact factor: 4.772

  2 in total

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