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1000 Titel
  • Complete lung agenesis caused by complex genomic rearrangements with neo-TAD formation at the SHH locus
1000 Autor/in
  1. Melo, Uirá Souto |
  2. Piard, Juliette |
  3. Fischer-Zirnsak, Björn |
  4. Klever, Marius-Konstantin |
  5. Schöpflin, Robert |
  6. Mensah, Martin Atta |
  7. Holtgrewe, Manuel |
  8. Arbez-Gindre, Francine |
  9. Martin, Alain |
  10. Guigue, Virginie |
  11. Gaillard, Dominique |
  12. Landais, Emilie |
  13. Roze, Virginie |
  14. Kremer, Valerie |
  15. Ramanah, Rajeev |
  16. Cabrol, Christelle |
  17. Harms, Frederike L. |
  18. Kornak, Uwe |
  19. Spielmann, Malte |
  20. Mundlos, Stefan |
  21. Van Maldergem, Lionel |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-08-26
1000 Erschienen in
1000 Quellenangabe
  • 140(10):1459-1469
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00439-021-02344-6 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8460539/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • During human organogenesis, lung development is a timely and tightly regulated developmental process under the control of a large number of signaling molecules. Understanding how genetic variants can disturb normal lung development causing different lung malformations is a major goal for dissecting molecular mechanisms during embryogenesis. Here, through exome sequencing (ES), array CGH, genome sequencing (GS) and Hi-C, we aimed at elucidating the molecular basis of bilateral isolated lung agenesis in three fetuses born to a non-consanguineous family. We detected a complex genomic rearrangement containing duplicated, triplicated and deleted fragments involving the SHH locus in fetuses presenting complete agenesis of both lungs and near-complete agenesis of the trachea, diagnosed by ultrasound screening and confirmed at autopsy following termination. The rearrangement did not include SHH itself, but several regulatory elements for lung development, such as MACS1, a major SHH lung enhancer, and the neighboring genes MNX1 and NOM1. The rearrangement incorporated parts of two topologically associating domains (TADs) including their boundaries. Hi-C of cells from one of the affected fetuses showed the formation of two novel TADs each containing SHH enhancers and the MNX1 and NOM1 genes. Hi-C together with GS indicate that the new 3D conformation is likely causative for this condition by an inappropriate activation of MNX1 included in the neo-TADs by MACS1 enhancer, further highlighting the importance of the 3D chromatin conformation in human disease.
1000 Sacherschließung
lokal Female [MeSH]
lokal Lung/abnormalities [MeSH]
lokal Organogenesis/genetics [MeSH]
lokal Adult [MeSH]
lokal Abnormalities, Multiple/genetics [MeSH]
lokal Fetus [MeSH]
lokal Humans [MeSH]
lokal Molecular Medicine
lokal Evolution, Molecular [MeSH]
lokal Genome, Human [MeSH]
lokal Original Investigation
lokal Male [MeSH]
lokal Metabolic Diseases
lokal Lung Diseases/genetics [MeSH]
lokal Gene Function
lokal Cadaver [MeSH]
lokal Lung/growth
lokal Genetic Variation [MeSH]
lokal Pregnancy [MeSH]
lokal Lung/ultrastructure [MeSH]
lokal Human Genetics
1000 Liste der Beteiligten
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1000 Erstellt am 2023-04-28T14:17:37.905+0200
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1000 Zuletzt bearbeitet Fri Oct 20 19:04:58 CEST 2023
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