Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex

被引:25
|
作者
Kapoor, Saketh [1 ]
Shah, Mohd Hussain [1 ]
Singh, Nivedita [1 ]
Rather, Mohammad Iqbal [1 ]
Bhat, Vishwanath [1 ]
Gopinath, Sindhura [2 ]
Bindu, Parayil Sankaran [3 ]
Taly, Arun B. [3 ]
Sinha, Sanjib [3 ]
Nagappa, Madhu [3 ]
Bharath, Rose Dawn [4 ]
Mahadevan, Anita [5 ]
Narayanappa, Gayathri [5 ]
Chickabasaviah, Yasha T. [5 ]
Kumar, Arun [1 ]
机构
[1] Indian Inst Sci, Dept Mol Reprod Dev & Genet, Bangalore 560012, Karnataka, India
[2] RV Coll Engn, Dept Biotechnol, Bangalore 560059, Karnataka, India
[3] Natl Inst Mental Hlth & Neurosci, Dept Neurol, Bangalore 560029, Karnataka, India
[4] Natl Inst Mental Hlth & Neurosci, Dept Neuroimaging & Intervent Radiol, Bangalore 560029, Karnataka, India
[5] Natl Inst Mental Hlth & Neurosci, Dept Neuropathol, Bangalore 560029, Karnataka, India
来源
PLOS ONE | 2016年 / 11卷 / 05期
关键词
PHOSPHOLIPASE A(2); PHENOTYPIC SPECTRUM; MUTATION; MODEL;
D O I
10.1371/journal.pone.0155605
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mutations in PLA2G6 were identified in patients with a spectrum of neurodegenerative conditions, such as infantile neuroaxonal dystrophy (INAD), atypical late-onset neuroaxonal dystrophy (ANAD) and dystonia parkinsonism complex (DPC). However, there is no report on the genetic analysis of families with members affected with INAD, ANAD and DPC from India. Therefore, the main aim of this study was to perform genetic analysis of 22 Indian families with INAD, ANAD and DPC. DNA sequence analysis of the entire coding region of PLA2G6 identified 13 different mutations, including five novel ones (p.Leu224Pro, p.Asp283Asn, p.Arg329Cys, p.Leu491Phe, and p.Arg649His), in 12/22 (54.55%) families with INAD and ANAD. Interestingly, one patient with INAD was homozygous for two different mutations, p.Leu491Phe and p.Ala516Val, and thus harboured four mutant alleles. With these mutations, the total number of mutations in this gene reaches 129. The absence of mutations in 10/22 (45.45%) families suggests that the mutations could be in deep intronic or promoter regions of this gene or these families could have mutations in a yet to be identified gene. The present study increases the mutation landscape of PLA2G6. The present finding will be useful for genetic diagnosis, carrier detection and genetic counselling to families included in this study and other families with similar disease condition.
引用
收藏
页数:12
相关论文
共 50 条
  • [11] Novel insertion mutation in the PLA2G6 gene in an Iranian family with infantile neuroaxonal dystrophy
    Rostampour, Dorsa
    Zolfaghari, Mohammad Reza
    Gholami, Milad
    JOURNAL OF CLINICAL LABORATORY ANALYSIS, 2022, 36 (03)
  • [12] Iron accumulation and neuroaxonal dystrophy in PLA2G6 associated neurodegeneration
    Sumi-Akamaru, H.
    Beck, G.
    Riku, Y.
    Yoshida, M.
    Fujimura, H.
    Kato, S.
    Mochizuki, H.
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2017, 381 : 738 - 739
  • [13] Phenotypic spectrum of patients with infantile neuroaxonal dystrophy (INAD) caused by mutations in the PLA2G6 gene
    Kurian, M. A.
    Morgan, N., V
    Wassmer, E.
    MacPherson, L.
    Peake, D.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2007, 30 : 141 - 141
  • [14] Infantile neuroaxonal dystrophy caused by PLA2G6 gene mutation in a Chinese patient: A case report
    Wang, Baotian
    Wu, De
    Tang, Jiulai
    EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2018, 16 (02) : 1290 - 1294
  • [15] A new missense mutation in PLA2G6 gene among a family with infantile neuroaxonal dystrophy INAD
    Gebril, Ola
    Uebe, Steffen
    Reuter, Miriam
    Schumacher, Johannes
    Abou Jamra, Rami
    Reis, Andre
    EGYPTIAN PEDIATRIC ASSOCIATION GAZETTE, 2016, 64 (04) : 171 - 176
  • [16] A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy (vol 381, pg 209, 2017)
    Iannello, Grazia
    Graziano, Claudio
    Cenacchi, Giovanna
    Cordelli, Duccio Maria
    Zuntini, Roberta
    Papa, Valentina
    Magista, Anna Maria
    Gagliardi, Monica
    Procopio, Radha
    Quattrone, Aldo
    Annesi, Grazia
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2018, 385 : 238 - 238
  • [17] Identification of a Novel Nonsense Mutation in PLA2G6 and Prenatal Diagnosis in a Chinese Family With Infantile Neuroaxonal Dystrophy
    Zou, Yongyi
    Luo, Haiyan
    Yuan, Huizhen
    Xie, Kang
    Yang, Yan
    Huang, Shuhui
    Yang, Bicheng
    Liu, Yanqiu
    FRONTIERS IN NEUROLOGY, 2022, 13
  • [18] Fetal Akinesia Deformation Sequence and Neuroaxonal Dystrophy without PLA2G6 Mutation
    Rakheja, Dinesh
    Uddin, Naseem
    Mitui, Midori
    Cope-Yokoyama, Sandy
    Hogan, Robert N.
    Burns, Dennis K.
    PEDIATRIC AND DEVELOPMENTAL PATHOLOGY, 2010, 13 (06) : 492 - 496
  • [19] A rare inherited homozygous missense variant in PLA2G6 influences susceptibility to infantile neuroaxonal dystrophy: a case report
    Lyu, Yongxue
    Wang, Tao
    Lin, Meifang
    Qi, Fengfeng
    TRANSLATIONAL PEDIATRICS, 2024, 13 (03) : 484 - 491
  • [20] Cerebellar atrophy without cerebellar cortex hyperintensity in infantile neuroaxonal dystrophy (INAD) due to PLA2G6 mutation
    Biancheri, Roberta
    Rossi, Andrea
    Alpigiani, Giannina
    Filocamo, Mirella
    Gandolfo, Carlo
    Lorini, Renata
    Minetti, Carlo
    EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, 2007, 11 (03) : 175 - 177