Literature DB >> 29872134

Identification of predominant GNPTAB gene mutations in Eastern Chinese patients with mucolipidosis II/III and a prenatal diagnosis of mucolipidosis II.

Yu Wang1, Jun Ye1, Wen-Juan Qiu1, Lian-Shu Han1, Xiao-Lan Gao1, Li-Li Liang1, Xue-Fan Gu2, Hui-Wen Zhang3.   

Abstract

Mucolipidosis II α/β, mucolipidosis III α/β, and mucolipidosis III γ are autosomal recessive disorders belonging to the family of lysosomal storage disorders caused by deficiency of the UDP-N-acetylglucosamine, a lysosomal enzyme N-acetylglucosamine-1-phosphotransferase (GlcNAc-phosphotransferase) localized in the Golgi apparatus, which is essential for normal processing and packaging of soluble lysosomal enzymes with initiating the first step of tagging lysosomal enzymes with mannose-6-phosphate (M6P). Mucolipidosis II and III are caused by mutations in the GNPTAB and GNPTG genes, and patients with these diseases are characterized by short stature, skeletal abnormalities, and developmental delay. In this study we report 38 patients with mucolipidosis II and III enrolled in Eastern China during the past 8 years. The diagnosis was made based on clinical characteristics and measurement of plasma lysosomal enzyme activity. Sanger sequencing of GNPTAB and/or GNPTG for all patients and real-time quantitative PCR were performed to confirm the diagnosis. In addition, 11 cases of prenatal mucolipidosis II were diagnosed based on measurement of the enzyme activity in amniotic fluid supernatant and genetic testing of cultured amniotic cells. Based on molecular genetic tests, 30 patients were diagnosed with mucolipidosis II α/β, 6 were diagnosed with III α/β and 2 were diagnosed with III γ. Thirty-seven different GNPTAB gene mutations were identified in 29 patients with mucolipidosis II α/β and six patients with III α/β. These mutations included 22 new mutations (p.W44X, p.E279X, p.W416X, p.W463X, p.Q802X, p.Q882X, p.A34P, p.R334P, p.D408N, p.D534N, p.Y997C, p.D1018V, p.L1025S, p.L1033P, c.88_89delAC, c.890_891insT, c.1150_1151insTTA, c.1523delG, c.2473_2474insA, c.2980_2983delGCCT, c.3094delA, and deletion of exon 9). Four new GNPTG gene mutations were identified (c.13delC, p.Y81X, p.G126R and c.609+1delG) in two mucolipidosis III γ patients. Among the 11 cases of prenatal diagnosis, four were mucolipidosis II fetuses, three were heterozygous, and the remaining four were normal fetuses. This study expands the mutation spectrum of the GNPTAB and GNPTG genes and contributes to specific knowledge of mucolipidosis II/III in a population from Eastern China.

Entities:  

Keywords:  GNPTAB; GNPTG; gene mutation; genotype; lysosomal enzymes; mucolipidosis; phenotype; prenatal diagnosis

Mesh:

Substances:

Year:  2018        PMID: 29872134      PMCID: PMC6329779          DOI: 10.1038/s41401-018-0023-9

Source DB:  PubMed          Journal:  Acta Pharmacol Sin        ISSN: 1671-4083            Impact factor:   6.150


  37 in total

1.  Genomic organisation of the UDP-N-acetylglucosamine-1-phosphotransferase gamma subunit (GNPTAG) and its mutations in mucolipidosis III.

Authors:  A Raas-Rothschild; R Bargal; O Goldman; E Ben-Asher; J E M Groener; A Toutain; E Stemmer; Z Ben-Neriah; H Flusser; F A Beemer; M Penttinen; T Olender; A J J T Rein; G Bach; M Zeigler
Journal:  J Med Genet       Date:  2004-04       Impact factor: 6.318

2.  Identification of mutations in the GNPTA (MGC4170) gene coding for GlcNAc-phosphotransferase alpha/beta subunits in Korean patients with mucolipidosis type II or type IIIA.

Authors:  Kyung Hoon Paik; Seng Mi Song; Chang Seok Ki; Han-Wook Yu; Jung Sim Kim; Ki Hoon Min; Soo Hee Chang; Eun Jae Yoo; In Jung Lee; Eun Kyung Kwan; Sun Joo Han; Dong-Kyu Jin
Journal:  Hum Mutat       Date:  2005-10       Impact factor: 4.878

3.  Diagnosis of alpha-mannosidosis by measuring alpha-mannosidase in plasma.

Authors:  E M Prence; M R Natowicz
Journal:  Clin Chem       Date:  1992-04       Impact factor: 8.327

4.  Mucolipidosis II is caused by mutations in GNPTA encoding the alpha/beta GlcNAc-1-phosphotransferase.

Authors:  Stephan Tiede; Stephan Storch; Torben Lübke; Bernard Henrissat; Ruth Bargal; Annick Raas-Rothschild; Thomas Braulke
Journal:  Nat Med       Date:  2005-10-02       Impact factor: 53.440

5.  Missense mutations in N-acetylglucosamine-1-phosphotransferase alpha/beta subunit gene in a patient with mucolipidosis III and a mild clinical phenotype.

Authors:  Stephan Tiede; Nicole Muschol; Gert Reutter; Michael Cantz; Kurt Ullrich; Thomas Braulke
Journal:  Am J Med Genet A       Date:  2005-09-01       Impact factor: 2.802

6.  Molecular basis of variant pseudo-hurler polydystrophy (mucolipidosis IIIC)

Authors:  A Raas-Rothschild; V Cormier-Daire; M Bao; E Genin; R Salomon; K Brewer; M Zeigler; H Mandel; S Toth; B Roe; A Munnich; W M Canfield
Journal:  J Clin Invest       Date:  2000-03       Impact factor: 14.808

7.  The alpha- and beta-subunits of the human UDP-N-acetylglucosamine:lysosomal enzyme N-acetylglucosamine-1-phosphotransferase [corrected] are encoded by a single cDNA.

Authors:  Mariko Kudo; Ming Bao; Anil D'Souza; Fu Ying; Huaqin Pan; Bruce A Roe; William M Canfield
Journal:  J Biol Chem       Date:  2005-08-24       Impact factor: 5.157

8.  Mucolipidosis II presenting as severe neonatal hyperparathyroidism.

Authors:  Sheila Unger; David A Paul; Michelle C Nino; Charles P McKay; Stephen Miller; Etienne Sochett; Nancy Braverman; Joe T R Clarke; David E C Cole; Andrea Superti-Furga
Journal:  Eur J Pediatr       Date:  2004-12-03       Impact factor: 3.183

9.  Clinical variability in mucolipidosis III (pseudo-Hurler polydystrophy).

Authors:  Anna Tylki-Szymańska; Barbara Czartoryska; Johanna E M Groener; Agnieszka Ługowska
Journal:  Am J Med Genet       Date:  2002-03-15

10.  A single site in human beta-hexosaminidase A binds both 6-sulfate-groups on hexosamines and the sialic acid moiety of GM2 ganglioside.

Authors:  Rohita Sharma; Scott Bukovac; John Callahan; Don Mahuran
Journal:  Biochim Biophys Acta       Date:  2003-01-20
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  6 in total

1.  Disease-causing missense mutations within the N-terminal transmembrane domain of GlcNAc-1-phosphotransferase impair endoplasmic reticulum translocation or Golgi retention.

Authors:  Wang-Sik Lee; Benjamin C Jennings; Balraj Doray; Stuart Kornfeld
Journal:  Hum Mutat       Date:  2020-04-08       Impact factor: 4.878

2.  Structure of the human GlcNAc-1-phosphotransferase αβ subunits reveals regulatory mechanism for lysosomal enzyme glycan phosphorylation.

Authors:  Hua Li; Wang-Sik Lee; Xiang Feng; Lin Bai; Benjamin C Jennings; Lin Liu; Balraj Doray; William M Canfield; Stuart Kornfeld; Huilin Li
Journal:  Nat Struct Mol Biol       Date:  2022-03-24       Impact factor: 18.361

3.  Placental pathology in an unsuspected case of mucolipidosis type II with secondary hyperparathyroidism in a premature infant.

Authors:  Parith Wongkittichote; Garland Michael Upchurch; Louis P Dehner; Timothy Wood; Jorge L Granadillo
Journal:  Mol Genet Metab Rep       Date:  2021-03-25

4.  Case Report: Mucolipidosis II and III Alpha/Beta Caused by Pathogenic Variants in the GNPTAB Gene (Mucolipidosis).

Authors:  Shao-Jia Mao; Yu-Mei Zu; Yang-Li Dai; Chao-Chun Zou
Journal:  Front Pediatr       Date:  2022-04-08       Impact factor: 3.418

Review 5.  Detection of Structural Variants by NGS: Revealing Missing Alleles in Lysosomal Storage Diseases.

Authors:  Valentina La Cognata; Sebastiano Cavallaro
Journal:  Biomedicines       Date:  2022-07-29

6.  GNPTAB c.2404C > T nonsense mutation in a patient with mucolipidosis III alpha/beta: a case report.

Authors:  Chi-Chun Ho; Lilian Li-Yan Tsung; Kam-Tim Liu; Wing-Tat Poon
Journal:  BMC Med Genet       Date:  2018-09-12       Impact factor: 2.103

  6 in total

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