Non-Syndromic Intellectual Disability and Its Pathways: A Long Noncoding RNA Perspective

被引:5
|
作者
Barros, Isabela I. [1 ]
Leao, Vitor [1 ]
Santis, Jessica O. [1 ]
Rosa, Reginaldo C. A. [1 ]
Brotto, Danielle B. [1 ]
Storti, Camila B. [1 ]
Siena, Adamo D. D. [1 ]
Molfetta, Greice A. [1 ]
Silva, Wilson A., Jr. [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Univ Sao Paulo, Ribeirao Preto Med Sch, Dept Genet, Ave Bandeirantes 3900, BR-14049900 Ribeirao Preto, SP, Brazil
[2] Univ Sao Paulo, Natl Inst Sci & Technol Stem Cell & Cell Therapy, Ribeirao Preto Med Sch, Rua Tenente Catao Roxo 2501, BR-14051140 Ribeirao Preto, Brazil
[3] Univ Sao Paulo, Ribeirao Preto Med Sch, Ctr Cell Based Therapy, Rua Tenente Catao Roxo 2501, BR-14051140 Ribeirao Preto, Brazil
[4] Univ Sao Paulo, Ribeirao Preto Med Sch, Ctr Integrat Syst Biol CISBi, NAP USP, Rua Catao Roxo 2501, BR-14051140 Ribeirao Preto, Brazil
[5] Midwest State Univ Parana UNICTR, Dept Med, Rua Fortim Atalaia 1900,Cidade Lagos, BR-85100000 Guarapuava, Brazil
[6] Guarapuava Inst Canc Res, Rua Fortim Atalaia 1900,Cidade Lagos, BR-85100000 Guarapuava, Brazil
基金
巴西圣保罗研究基金会;
关键词
SONIC HEDGEHOG; SIGNALING PATHWAY; BRAIN-DEVELOPMENT; NERVOUS-SYSTEM; RETT-SYNDROME; RHO-GTPASES; NEURODEVELOPMENTAL DISORDERS; PROGENITOR PROLIFERATION; PROMOTES PROLIFERATION; NEURONAL DEVELOPMENT;
D O I
10.3390/ncrna7010022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Non-syndromic intellectual disability (NS-ID or idiopathic) is a complex neurodevelopmental disorder that represents a global health issue. Although many efforts have been made to characterize it and distinguish it from syndromic intellectual disability (S-ID), the highly heterogeneous aspect of this disorder makes it difficult to understand its etiology. Long noncoding RNAs (lncRNAs) comprise a large group of transcripts that can act through various mechanisms and be involved in important neurodevelopmental processes. In this sense, comprehending the roles they play in this intricate context is a valuable way of getting new insights about how NS-ID can arise and develop. In this review, we attempt to bring together knowledge available in the literature about lncRNAs involved with molecular and cellular pathways already described in intellectual disability and neural function, to better understand their relevance in NS-ID and the regulatory complexity of this disorder.
引用
收藏
页数:22
相关论文
共 50 条
  • [1] Alterations to synaptic vesicles pathways are likely to be involved in non-syndromic intellectual disability
    Zelenova, M. A.
    Vorsanova, S. G.
    Yurov, Y. B.
    Korostelev, S. A.
    Kurinnaia, O. S.
    Iourov, I. Y.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 242 - 243
  • [2] The genetic basis of non-syndromic intellectual disability: a review
    Kaufman, Liana
    Ayub, Muhammad
    Vincent, John B.
    JOURNAL OF NEURODEVELOPMENTAL DISORDERS, 2010, 2 (04) : 182 - 209
  • [3] Gene networks associated with non-syndromic intellectual disability
    Lee, Soohyun
    Rudd, Stephen
    Gratten, Jacob
    Visscher, Peter M.
    Prins, Johannes B.
    Dawson, Paul A.
    JOURNAL OF NEUROGENETICS, 2018, 32 (01) : 6 - 14
  • [4] The genetic basis of non-syndromic intellectual disability: a review
    Liana Kaufman
    Muhammad Ayub
    John B. Vincent
    Journal of Neurodevelopmental Disorders, 2010, 2 : 182 - 209
  • [5] Uptake of funded genomic testing for syndromic and non-syndromic intellectual disability in Australia
    Dylan A. Mordaunt
    Kim Dalziel
    Ilias Goranitis
    Zornitza Stark
    European Journal of Human Genetics, 2023, 31 : 977 - 979
  • [6] Uptake of funded genomic testing for syndromic and non-syndromic intellectual disability in Australia
    Mordaunt, Dylan A.
    Dalziel, Kim
    Goranitis, Ilias
    Stark, Zornitza
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 (09) : 977 - 979
  • [7] Mutations of ARX and non-syndromic intellectual disability in Chinese population
    Yufei Wu
    Huan Zhang
    Xiaofen Liu
    Zhangyan Shi
    Hongling Li
    Zhibin Wang
    Xiaoyong Jie
    Shaoping Huang
    Fuchang Zhang
    Junlin Li
    Kejin Zhang
    Xiaocai Gao
    Genes & Genomics, 2019, 41 : 125 - 131
  • [8] Mutations of ARX and non-syndromic intellectual disability in Chinese population
    Wu, Yufei
    Zhang, Huan
    Liu, Xiaofen
    Shi, Zhangyan
    Li, Hongling
    Wang, Zhibin
    Jie, Xiaoyong
    Huang, Shaoping
    Zhang, Fuchang
    Li, Junlin
    Zhang, Kejin
    Gao, Xiaocai
    GENES & GENOMICS, 2019, 41 (01) : 125 - 131
  • [9] Evaluation of Individuals with Non-Syndromic Global Developmental Delay and Intellectual Disability
    AlMutiri, Rowim
    Malta, Maisa
    Shevell, Michael I.
    Srour, Myriam
    CHILDREN-BASEL, 2023, 10 (03):
  • [10] WDR13: A Novel Gene Implicated in Non-Syndromic Intellectual Disability
    Rzonca-Niewczas, Sylwia
    Wierzba, Jolanta
    Kaczorowska, Ewa
    Poryszewska, Milena
    Kosinska, Joanna
    Stawinski, Piotr
    Ploski, Rafal
    Bal, Jerzy
    GENES, 2021, 12 (12)