Literature DB >> 21665001

Hereditary leukonychia, or porcelain nails, resulting from mutations in PLCD1.

Maija Kiuru1, Mazen Kurban1, Munenari Itoh1, Lynn Petukhova1, Yutaka Shimomura1, Muhammad Wajid1, Angela M Christiano2.   

Abstract

Hereditary leukonychia (porcelain nails or white nails) is a rare nail disorder with an unknown genetic basis. To identify variants in a gene underlying this phenotype, we identified four families of Pakistani origin showing features of hereditary leukonychia. All 20 nails of each affected individual were chalky and white in appearance, consistent with total leukonychia, with no other cutaneous, appendageal, or systemic findings. By using Affymetrix 10K chip, we established linkage to chromosome 3p21.3-p22 with a LOD score (Z) of 5.1. We identified pathogenic mutations in PLCD1 in all four families, which encodes phosphoinositide-specific phospholipase C delta 1 subunit, a key enzyme in phosphoinositide metabolism. We then identified localization of PLCD1 in the nail matrix. It was recently shown that PLCD1 is a component of the human nail plate by proteomic analysis and is localized in the matrix of human nails. Furthermore, mutations detected in PLCD1 resulted in reduced enzymatic activity in vitro. Our data show that mutations in PLCD1 underlie hereditary leukonychia, revealing a gene involved in molecular control of nail growth.
Copyright © 2011 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21665001      PMCID: PMC3113240          DOI: 10.1016/j.ajhg.2011.05.014

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  29 in total

1.  LEUKONYCHIA. TOTAL AND PARTIAL LEUKONYCHIA IN A SINGLE FAMILY WITH A REVIEW OF THE LITERATURE.

Authors:  S D ALBRIGHT; C E WHEELER
Journal:  Arch Dermatol       Date:  1964-10

2.  Novel keratin 14 mutations in patients with severe recessive epidermolysis bullosa simplex.

Authors:  Cristina Has; Yow-Ren Chang; Andreas Volz; Doris Hoeping; Jürgen Kohlhase; Leena Bruckner-Tuderman
Journal:  J Invest Dermatol       Date:  2006-04-13       Impact factor: 8.551

3.  Mutations in the gene encoding the Wnt-signaling component R-spondin 4 (RSPO4) cause autosomal recessive anonychia.

Authors:  C Bergmann; J Senderek; D Anhuf; C T Thiel; A B Ekici; P Poblete-Gutierrez; M van Steensel; D Seelow; G Nürnberg; H H Schild; P Nürnberg; A Reis; J Frank; K Zerres
Journal:  Am J Hum Genet       Date:  2006-10-17       Impact factor: 11.025

4.  PLCD1 is a functional tumor suppressor inducing G(2)/M arrest and frequently methylated in breast cancer.

Authors:  Tingxiu Xiang; Lili Li; Yichao Fan; Yanyan Jiang; Ying Ying; Thomas C Putti; Qian Tao; Guosheng Ren
Journal:  Cancer Biol Ther       Date:  2010-09-21       Impact factor: 4.742

5.  Proteomic analysis of human nail plate.

Authors:  Robert H Rice; Yajuan Xia; Rudy J Alvarado; Brett S Phinney
Journal:  J Proteome Res       Date:  2010-11-01       Impact factor: 4.466

6.  Identification of a novel class of mammalian phosphoinositol-specific phospholipase C enzymes.

Authors:  Alan J Stewart; Joy Mukherjee; Scott J Roberts; Douglas Lester; Colin Farquharson
Journal:  Int J Mol Med       Date:  2005-01       Impact factor: 4.101

7.  Phospholipase C delta 1 is a novel 3p22.3 tumor suppressor involved in cytoskeleton organization, with its epigenetic silencing correlated with high-stage gastric cancer.

Authors:  X-T Hu; F-B Zhang; Y-C Fan; X-S Shu; A H Y Wong; W Zhou; Q-L Shi; H-M Tang; L Fu; X-Y Guan; S Y Rha; Q Tao; C He
Journal:  Oncogene       Date:  2009-05-18       Impact factor: 9.867

8.  ATM gene mutations result in both recessive and dominant expression phenotypes of genes and microRNAs.

Authors:  Denis A Smirnov; Vivian G Cheung
Journal:  Am J Hum Genet       Date:  2008-08       Impact factor: 11.025

9.  Hereditary leukonychia totalis, acanthosis-nigricans-like lesions and hair dysplasia: a new syndrome?

Authors:  Yannick Le Corre; Maud Steff; Anne Croue; Robert Filmon; Jean-Luc Verret; Christian Le Clech
Journal:  Eur J Med Genet       Date:  2009-05-04       Impact factor: 2.708

10.  Phospholipase C-delta1 is an essential molecule downstream of Foxn1, the gene responsible for the nude mutation, in normal hair development.

Authors:  Yoshikazu Nakamura; Manabu Ichinohe; Masayuki Hirata; Hirokazu Matsuura; Takashi Fujiwara; Takahiro Igarashi; Masamichi Nakahara; Hideki Yamaguchi; Sadao Yasugi; Tadaomi Takenawa; Kiyoko Fukami
Journal:  FASEB J       Date:  2007-10-15       Impact factor: 5.191

View more
  11 in total

1.  Spontaneous Quick Resolution of Uncombable Hair Syndrome-Like Disease.

Authors:  Yuval Ramot; Abraham Zlotogorski; Vered Molho-Pessach
Journal:  Skin Appendage Disord       Date:  2018-10-11

2.  An Idiopathic Leukonychia Totalis and Leukonychia Partialis Case Report and Review of the Literature.

Authors:  Theresa Canavan; Antonella Tosti; Hurst Mallory; Kristopher McKay; Wendy Cantrell; Boni Elewski
Journal:  Skin Appendage Disord       Date:  2015-03-27

3.  Whole exome sequencing identifies a novel dominant missense mutation underlying leukonychia in a Pakistani family.

Authors:  Teka Khan; Manan Khan; Ayesha Yousaf; Saadullah Khan; Muhammad Naeem; Akram Shah; Ghulam Murtaza; Asim Ali; Nazish Jabeen; Hafiz Muhammad Jafar Hussain; Hui Ma; Yuanwei Zhang; Muhammad Zubair; Xiaohua Jiang; Huan Zhang
Journal:  J Hum Genet       Date:  2018-07-23       Impact factor: 3.172

4.  [Leukonychia totalis].

Authors:  G Wagner; V Meyer; M M Sachse
Journal:  Hautarzt       Date:  2016-04       Impact factor: 0.751

5.  SERPINB11 frameshift variant associated with novel hoof specific phenotype in Connemara ponies.

Authors:  Carrie J Finno; Carlynn Stevens; Amy Young; Verena Affolter; Nikhil A Joshi; Sheila Ramsay; Danika L Bannasch
Journal:  PLoS Genet       Date:  2015-04-13       Impact factor: 5.917

6.  Idiopathic congenital true leukonychia totalis.

Authors:  Avhad Ganesh; Ghuge Priyanka
Journal:  Indian Dermatol Online J       Date:  2014-11

7.  Abnormalities of hair structure and skin histology derived from CRISPR/Cas9-based knockout of phospholipase C-delta 1 in mice.

Authors:  Yu-Min Liu; Wei Liu; Jun-Shuang Jia; Bang-Zhu Chen; Heng-Wei Chen; Yu Liu; Ya-Nan Bie; Peng Gu; Yan Sun; Dong Xiao; Wei-Wang Gu
Journal:  J Transl Med       Date:  2018-05-25       Impact factor: 5.531

8.  Hereditary Leukonychia Totalis: A Case Report and Review of the Literature.

Authors:  Kallapan Pakornphadungsit; Poonkiat Suchonwanit; Tueboon Sriphojanart; Pamela Chayavichitsilp
Journal:  Case Rep Dermatol       Date:  2018-04-12

9.  Mutation in Phospholipase C, δ1 (PLCD1) Gene Underlies Hereditary Leukonychia in a Pashtun Family and Review of the Literature.

Authors:  A K Khan; S A Khan; Na Muhammad; No Muhammad; J Ahmad; H Nawaz; A Nasir; S Farman; S Khan
Journal:  Balkan J Med Genet       Date:  2018-10-29       Impact factor: 0.519

10.  Identification of two novel mutations in the PLCD1 gene in Chinese patients with hereditary leukonychia.

Authors:  Shuzhan Shen; Minhua Shao; Uma Keyal; Xiuli Wang; Ming Li; Guolong Zhang
Journal:  Mol Med Rep       Date:  2021-03-31       Impact factor: 2.952

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.