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Identification of Variants in RET and IHH Pathway Members in a Large Family With History of Hirschsprung Disease

Sribudiani, Y., Chauhan, R. K., Alves, M. M., Petrova, L., Brosens, E., Harrison, C., Wabbersen, T., de Graaf, B. M., Rugenbrink, T., Burzynski, G., Brouwer, R. W. W., van IJcken, W. F. J., Maas, S. M., de Klein, A., Osinga, J., Eggen, B. J. L., Burns, A. J., Brooks, A. S., Shepherd, I. T. & Hofstra, R. M. W., Jul-2018, In : Gastroenterology. 155, 1, p. 118-129.e6 18 p.

Research output: Contribution to journalArticleAcademicpeer-review

  • Yunia Sribudiani
  • Rajendra K. Chauhan
  • Maria M. Alves
  • Lucy Petrova
  • Erwin Brosens
  • Colin Harrison
  • Tara Wabbersen
  • Bianca M. de Graaf
  • Tim Rugenbrink
  • Grzegorz Burzynski
  • Rutger W. W. Brouwer
  • Wilfred F. J. van IJcken
  • Saskia M. Maas
  • Annelies de Klein
  • Jan Osinga
  • Bart J. L. Eggen
  • Alan J. Burns
  • Alice S. Brooks
  • Iain T. Shepherd
  • Robert M. W. Hofstra

BACKGROUND & AIMS: Hirschsprung disease (HSCR) is an inherited congenital disorder characterized by absence of enteric ganglia in the distal part of the gut. Variants in ret proto-oncogene (RET) have been associated with up to 50% of familial and 35% of sporadic cases. We searched for variants that affect disease risk in a large, multigenerational family with history of HSCR in a linkage region previously associated with the disease (4q31.3-q32.3) and exome wide. METHODS: We performed exome sequencing analyses of a family in the Netherlands with 5 members diagnosed with HSCR and 2 members diagnosed with functional constipation. We initially focused on variants in genes located in 4q31.3-q32.3; however, we also performed an exome-wide analysis in which known HSCR or HSCR-associated gene variants predicted to be deleterious were prioritized for further analysis. Candidate genes were expressed in HEK293, COS-7, and Neuro-2a cells and analyzed by luciferase and immunoblot assays. Morpholinos were designed to target exons of candidate genes and injected into 1-cell stage zebrafish embryos. Embryos were allowed to develop and stained for enteric neurons. RESULTS: Within the linkage region, we identified 1 putative splice variant in the lipopolysaccharide responsive beige-like anchor protein gene (LRBA). Functional assays could not confirm its predicted effect on messenger RNA splicing or on expression of the mab-21 like 2 gene (MAB21L2), which is embedded in LRBA. Zebrafish that developed following injection of the lrba morpholino had a shortened body axis and subtle gut morphological defects, but no significant reduction in number of enteric neurons compared with controls. Outside the linkage region, members of 1 branch of the family carried a previously unidentified RET variant or an in-frame deletion in the glial cell line derived neurotrophic factor gene (GDNF), which encodes a ligand of RET. This deletion was located 6 base pairs before the last codon. We also found variants in the Indian hedgehog gene (IHH) and its mediator, the transcription factor GLI family zinc finger 3 (GLI3). When expressed in cells, the RET-P399L variant disrupted protein glycosylation and had altered phosphorylation following activation by GDNF. The deletion in GDNF prevented secretion of its gene product, reducing RET activation, and the IHH-Q51K variant reduced expression of the transcription factor GLI1. Injection of morpholinos that target ihh reduced the number of enteric neurons to 13% +/- 1.4% of control zebrafish. CONCLUSIONS: In a study of a large family with history of HSCR, we identified variants in LRBA, RET, the gene encoding the RET ligand (GDNF), IHH, and a gene encoding a mediator of IHH signaling (GLI3). These variants altered functions of the gene products when expressed in cells and knockout of ihh reduced the number of enteric neurons in the zebrafish gut.

Original languageEnglish
Pages (from-to)118-129.e6
Number of pages18
JournalGastroenterology
Volume155
Issue number1
Publication statusPublished - Jul-2018

    Keywords

  • ENS, Neural Development, Genetic Causes of HSCR, Family Study, NERVOUS-SYSTEM DEVELOPMENT, GENOME-WIDE ASSOCIATION, MULTIGENIC INHERITANCE, SUSCEPTIBILITY LOCUS, GERMLINE MUTATIONS, POINT MUTATIONS, GENE-EXPRESSION, ZEBRAFISH, PROTOONCOGENE, HEDGEHOG

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