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Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma

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Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma. / Pohler, Elizabeth; Mamai, Ons; Hirst, Jennifer; Zamiri, Mozheh; Horn, Helen; Nomura, Toshifumi; Irvine, Alan D; Moran, Benvon; Wilson, Neil J; Smith, Frances J D; Goh, Christabelle S M; Sandilands, Aileen; Cole, Christian; Barton, Geoffrey J; Evans, Alan T; Shimizu, Hiroshi; Akiyama, Masashi; Suehiro, Mitsuhiro; Konohana, Izumi; Shboul, Mohammad; Teissier, Sebastien; Boussofara, Lobna; Denguezli, Mohamed; Saad, Ali; Gribaa, Moez; Dopping-Hepenstal, Patricia J; McGrath, John A; Brown, Sara J; Goudie, David R; Reversade, Bruno; Munro, Colin S; McLean, W H Irwin (Lead / Corresponding author).

In: Nature Genetics, Vol. 44, No. 11, 11.2012, p. 1272-1276.

Research output: Contribution to journalArticle

Harvard

Pohler, E, Mamai, O, Hirst, J, Zamiri, M, Horn, H, Nomura, T, Irvine, AD, Moran, B, Wilson, NJ, Smith, FJD, Goh, CSM, Sandilands, A, Cole, C, Barton, GJ, Evans, AT, Shimizu, H, Akiyama, M, Suehiro, M, Konohana, I, Shboul, M, Teissier, S, Boussofara, L, Denguezli, M, Saad, A, Gribaa, M, Dopping-Hepenstal, PJ, McGrath, JA, Brown, SJ, Goudie, DR, Reversade, B, Munro, CS & McLean, WHI 2012, 'Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma' Nature Genetics, vol 44, no. 11, pp. 1272-1276.

APA

Pohler, E., Mamai, O., Hirst, J., Zamiri, M., Horn, H., Nomura, T., Irvine, A. D., Moran, B., Wilson, N. J., Smith, F. J. D., Goh, C. S. M., Sandilands, A., Cole, C., Barton, G. J., Evans, A. T., Shimizu, H., Akiyama, M., Suehiro, M., Konohana, I., Shboul, M., Teissier, S., Boussofara, L., Denguezli, M., Saad, A., Gribaa, M., Dopping-Hepenstal, P. J., McGrath, J. A., Brown, S. J., Goudie, D. R., Reversade, B., Munro, C. S., & McLean, W. H. I. (2012). Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma. Nature Genetics, 44(11), 1272-1276doi: 10.1038/ng.2444

Vancouver

Pohler E, Mamai O, Hirst J, Zamiri M, Horn H, Nomura T et al. Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma. Nature Genetics. 2012 Nov;44(11):1272-1276.

Author

Pohler, Elizabeth; Mamai, Ons; Hirst, Jennifer; Zamiri, Mozheh; Horn, Helen; Nomura, Toshifumi; Irvine, Alan D; Moran, Benvon; Wilson, Neil J; Smith, Frances J D; Goh, Christabelle S M; Sandilands, Aileen; Cole, Christian; Barton, Geoffrey J; Evans, Alan T; Shimizu, Hiroshi; Akiyama, Masashi; Suehiro, Mitsuhiro; Konohana, Izumi; Shboul, Mohammad; Teissier, Sebastien; Boussofara, Lobna; Denguezli, Mohamed; Saad, Ali; Gribaa, Moez; Dopping-Hepenstal, Patricia J; McGrath, John A; Brown, Sara J; Goudie, David R; Reversade, Bruno; Munro, Colin S; McLean, W H Irwin (Lead / Corresponding author) / Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma.

In: Nature Genetics, Vol. 44, No. 11, 11.2012, p. 1272-1276.

Research output: Contribution to journalArticle

Bibtex - Download

@article{bcaf90410a9349dea232224f90f48d3a,
title = "Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma",
author = "Elizabeth Pohler and Ons Mamai and Jennifer Hirst and Mozheh Zamiri and Helen Horn and Toshifumi Nomura and Irvine, {Alan D} and Benvon Moran and Wilson, {Neil J} and Smith, {Frances J D} and Goh, {Christabelle S M} and Aileen Sandilands and Christian Cole and Barton, {Geoffrey J} and Evans, {Alan T} and Hiroshi Shimizu and Masashi Akiyama and Mitsuhiro Suehiro and Izumi Konohana and Mohammad Shboul and Sebastien Teissier and Lobna Boussofara and Mohamed Denguezli and Ali Saad and Moez Gribaa and Dopping-Hepenstal, {Patricia J} and McGrath, {John A} and Brown, {Sara J} and Goudie, {David R} and Bruno Reversade and Munro, {Colin S} and McLean, {W H Irwin}",
year = "2012",
volume = "44",
number = "11",
pages = "1272--1276",
journal = "Nature Genetics",
issn = "1061-4036",

}

RIS (suitable for import to EndNote) - Download

TY - JOUR

T1 - Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma

A1 - Pohler,Elizabeth

A1 - Mamai,Ons

A1 - Hirst,Jennifer

A1 - Zamiri,Mozheh

A1 - Horn,Helen

A1 - Nomura,Toshifumi

A1 - Irvine,Alan D

A1 - Moran,Benvon

A1 - Wilson,Neil J

A1 - Smith,Frances J D

A1 - Goh,Christabelle S M

A1 - Sandilands,Aileen

A1 - Cole,Christian

A1 - Barton,Geoffrey J

A1 - Evans,Alan T

A1 - Shimizu,Hiroshi

A1 - Akiyama,Masashi

A1 - Suehiro,Mitsuhiro

A1 - Konohana,Izumi

A1 - Shboul,Mohammad

A1 - Teissier,Sebastien

A1 - Boussofara,Lobna

A1 - Denguezli,Mohamed

A1 - Saad,Ali

A1 - Gribaa,Moez

A1 - Dopping-Hepenstal,Patricia J

A1 - McGrath,John A

A1 - Brown,Sara J

A1 - Goudie,David R

A1 - Reversade,Bruno

A1 - Munro,Colin S

A1 - McLean,W H Irwin

AU - Pohler,Elizabeth

AU - Mamai,Ons

AU - Hirst,Jennifer

AU - Zamiri,Mozheh

AU - Horn,Helen

AU - Nomura,Toshifumi

AU - Irvine,Alan D

AU - Moran,Benvon

AU - Wilson,Neil J

AU - Smith,Frances J D

AU - Goh,Christabelle S M

AU - Sandilands,Aileen

AU - Cole,Christian

AU - Barton,Geoffrey J

AU - Evans,Alan T

AU - Shimizu,Hiroshi

AU - Akiyama,Masashi

AU - Suehiro,Mitsuhiro

AU - Konohana,Izumi

AU - Shboul,Mohammad

AU - Teissier,Sebastien

AU - Boussofara,Lobna

AU - Denguezli,Mohamed

AU - Saad,Ali

AU - Gribaa,Moez

AU - Dopping-Hepenstal,Patricia J

AU - McGrath,John A

AU - Brown,Sara J

AU - Goudie,David R

AU - Reversade,Bruno

AU - Munro,Colin S

AU - McLean,W H Irwin

PY - 2012/11

Y1 - 2012/11

N2 - Palmoplantar keratodermas (PPKs) are a group of disorders that are diagnostically and therapeutically problematic in dermatogenetics. Punctate PPKs are characterized by circumscribed hyperkeratotic lesions on the palms and soles with considerable heterogeneity. In 18 families with autosomal dominant punctate PPK, we report heterozygous loss-of-function mutations in AAGAB, encoding a- and ?-adaptin-binding protein p34, located at a previously linked locus at 15q22. a- and ?-adaptin-binding protein p34, a cytosolic protein with a Rab-like GTPase domain, was shown to bind both clathrin adaptor protein complexes, indicating a role in membrane trafficking. Ultrastructurally, lesional epidermis showed abnormalities in intracellular vesicle biology. Immunohistochemistry showed hyperproliferation within the punctate lesions. Knockdown of AAGAB in keratinocytes led to increased cell division, which was linked to greatly elevated epidermal growth factor receptor (EGFR) protein expression and tyrosine phosphorylation. We hypothesize that p34 deficiency may impair endocytic recycling of growth factor receptors such as EGFR, leading to increased signaling and cellular proliferation.

AB - Palmoplantar keratodermas (PPKs) are a group of disorders that are diagnostically and therapeutically problematic in dermatogenetics. Punctate PPKs are characterized by circumscribed hyperkeratotic lesions on the palms and soles with considerable heterogeneity. In 18 families with autosomal dominant punctate PPK, we report heterozygous loss-of-function mutations in AAGAB, encoding a- and ?-adaptin-binding protein p34, located at a previously linked locus at 15q22. a- and ?-adaptin-binding protein p34, a cytosolic protein with a Rab-like GTPase domain, was shown to bind both clathrin adaptor protein complexes, indicating a role in membrane trafficking. Ultrastructurally, lesional epidermis showed abnormalities in intracellular vesicle biology. Immunohistochemistry showed hyperproliferation within the punctate lesions. Knockdown of AAGAB in keratinocytes led to increased cell division, which was linked to greatly elevated epidermal growth factor receptor (EGFR) protein expression and tyrosine phosphorylation. We hypothesize that p34 deficiency may impair endocytic recycling of growth factor receptors such as EGFR, leading to increased signaling and cellular proliferation.

KW - LOCUS

KW - EGFR

KW - MEMBRANE

KW - IDENTIFICATION

KW - ENDOCYTIC TRAFFICKING

KW - PROTEINS

KW - DESMOPLAKIN

KW - MUTATIONS

KW - GROWTH-FACTOR RECEPTOR

KW - OCCURS

U2 - 10.1038/ng.2444

DO - 10.1038/ng.2444

M1 - Article

JO - Nature Genetics

JF - Nature Genetics

SN - 1061-4036

IS - 11

VL - 44

SP - 1272

EP - 1276

ER -

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