Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma

Adrian A. Lahola-Chomiak, Tim Footz, Kim Nguyen-Phuoc, Gavin J. Neil, Baojian Fan, Keri F. Allen, David Greenfield, Richard K Parrish, Kevin Linkroum, Louis R. Pasquale, Ralf M. Leonhardt, Robert Ritch, Shari Javadiyan, Jamie E. Craig, W. T. Allison, Ordan J. Lehmann, Michael A. Walter, Janey L. Wiggs

Research output: Contribution to journalArticle

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Abstract

Pigmentary glaucoma (PG) is a common glaucoma subtype that results from release of pigment from the iris, called pigment dispersion syndrome (PDS), and its deposition throughout the anterior chamber of the eye. Although PG has a substantial heritable component, no causative genes have yet been identified. We used whole exome sequencing of two independent pedigrees to identify two premelanosome protein (PMEL) variants associated with heritable PDS/PG. PMEL encodes a key component of the melanosome, the organelle essential for melanin synthesis, storage and transport. Targeted screening of PMEL in three independent cohorts (n = 394) identified seven additional PDS/PG-associated non-synonymous variants. Five of the nine variants exhibited defective processing of the PMEL protein. In addition, analysis of PDS/PG-associated PMEL variants expressed in HeLa cells revealed structural changes to pseudomelanosomes indicating altered amyloid fibril formation in five of the nine variants. Introduction of 11-base pair deletions to the homologous pmela in zebrafish by the clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9 method caused profound pigmentation defects and enlarged anterior segments in the eye, further supporting PMEL's role in ocular pigmentation and function. Taken together, these data support a model in which missense PMEL variants represent dominant negative mutations that impair the ability of PMEL to form functional amyloid fibrils. While PMEL mutations have previously been shown to cause pigmentation and ocular defects in animals, this research is the first report of mutations in PMEL causing human disease.

Original languageEnglish (US)
Pages (from-to)1298-1311
Number of pages14
JournalHuman molecular genetics
Volume28
Issue number8
DOIs
StatePublished - Apr 15 2019

Fingerprint

Open Angle Glaucoma
Proteins
Pigmentation
Amyloid
Mutation
Clustered Regularly Interspaced Short Palindromic Repeats
Anterior Eye Segment
Exome
Melanosomes
Melanins
Anterior Chamber
Iris
Zebrafish
Pedigree
HeLa Cells
Base Pairing
Glaucoma
Organelles
Glaucoma-Related Pigment Dispersion Syndrome

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Genetics(clinical)

Cite this

Lahola-Chomiak, A. A., Footz, T., Nguyen-Phuoc, K., Neil, G. J., Fan, B., Allen, K. F., ... Wiggs, J. L. (2019). Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma. Human molecular genetics, 28(8), 1298-1311. https://doi.org/10.1093/hmg/ddy429

Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma. / Lahola-Chomiak, Adrian A.; Footz, Tim; Nguyen-Phuoc, Kim; Neil, Gavin J.; Fan, Baojian; Allen, Keri F.; Greenfield, David; Parrish, Richard K; Linkroum, Kevin; Pasquale, Louis R.; Leonhardt, Ralf M.; Ritch, Robert; Javadiyan, Shari; Craig, Jamie E.; Allison, W. T.; Lehmann, Ordan J.; Walter, Michael A.; Wiggs, Janey L.

In: Human molecular genetics, Vol. 28, No. 8, 15.04.2019, p. 1298-1311.

Research output: Contribution to journalArticle

Lahola-Chomiak, AA, Footz, T, Nguyen-Phuoc, K, Neil, GJ, Fan, B, Allen, KF, Greenfield, D, Parrish, RK, Linkroum, K, Pasquale, LR, Leonhardt, RM, Ritch, R, Javadiyan, S, Craig, JE, Allison, WT, Lehmann, OJ, Walter, MA & Wiggs, JL 2019, 'Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma', Human molecular genetics, vol. 28, no. 8, pp. 1298-1311. https://doi.org/10.1093/hmg/ddy429
Lahola-Chomiak, Adrian A. ; Footz, Tim ; Nguyen-Phuoc, Kim ; Neil, Gavin J. ; Fan, Baojian ; Allen, Keri F. ; Greenfield, David ; Parrish, Richard K ; Linkroum, Kevin ; Pasquale, Louis R. ; Leonhardt, Ralf M. ; Ritch, Robert ; Javadiyan, Shari ; Craig, Jamie E. ; Allison, W. T. ; Lehmann, Ordan J. ; Walter, Michael A. ; Wiggs, Janey L. / Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma. In: Human molecular genetics. 2019 ; Vol. 28, No. 8. pp. 1298-1311.
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AU - Lahola-Chomiak, Adrian A.

AU - Footz, Tim

AU - Nguyen-Phuoc, Kim

AU - Neil, Gavin J.

AU - Fan, Baojian

AU - Allen, Keri F.

AU - Greenfield, David

AU - Parrish, Richard K

AU - Linkroum, Kevin

AU - Pasquale, Louis R.

AU - Leonhardt, Ralf M.

AU - Ritch, Robert

AU - Javadiyan, Shari

AU - Craig, Jamie E.

AU - Allison, W. T.

AU - Lehmann, Ordan J.

AU - Walter, Michael A.

AU - Wiggs, Janey L.

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