赵宸滋, 张晴, 李志刚. NBAS基因的生物学功能和相关疾病的研究进展[J]. 罕见病研究, 2022, 1(3): 359-364. DOI: 10.12376/j.issn.2097-0501.2022.03.021
引用本文: 赵宸滋, 张晴, 李志刚. NBAS基因的生物学功能和相关疾病的研究进展[J]. 罕见病研究, 2022, 1(3): 359-364. DOI: 10.12376/j.issn.2097-0501.2022.03.021
ZHAO Chenzi, ZHANG Qing, LI Zhigang. Progress in Biological Functions of NBAS Gene and Related Diseases[J]. Journal of Rare Diseases, 2022, 1(3): 359-364. DOI: 10.12376/j.issn.2097-0501.2022.03.021
Citation: ZHAO Chenzi, ZHANG Qing, LI Zhigang. Progress in Biological Functions of NBAS Gene and Related Diseases[J]. Journal of Rare Diseases, 2022, 1(3): 359-364. DOI: 10.12376/j.issn.2097-0501.2022.03.021

NBAS基因的生物学功能和相关疾病的研究进展

Progress in Biological Functions of NBAS Gene and Related Diseases

  • 摘要: 神经母细胞瘤扩增序列(NBAS)是一个在神经母细胞瘤系发现的高度保守的基因,定位于人类2号染色体p24.3,编码Synaxin-18复合体的一个组成部分,其功能主要是参与高尔基体至内质网的逆向转运和无义介导的mRNA降解。NBAS基因在30余种组织中广泛表达,提示其可能在人体内行使重要的功能。2010年和2015年,NBAS先后被鉴定为SOPH综合征和发热相关急性肝衰竭的致病基因。近期发现,NBAS基因突变也会导致免疫系统受累,引发免疫缺陷。本文就NBAS基因的主要生物学功能、基因突变的致病性及致病机制进行综述。

     

    Abstract: Neuroblastoma-amplified sequence (NBAS) is a highly conserved gene firstly found in neuroblastoma, targeting on the human chromosome 2 p24.3 and encodes a protein that is a subunit of the Syntaxin 18 complex. The functions of NBAS include the involvement in transport of Golgi-to-Endoplasmic Reticulum retrograde and degradation of nonsense-mediated mRNA. NBAS gene is widely expressed in more than 30 tissues, suggesting that it may play an important role in human body. In 2010 and 2015, NBAS was identified successively as the pathogenic gene of SOPH syndrome and fever-related liver failure respectively. Recent studies shows that NBAS gene mutations can involve immune system and cause immune deficiency. In this paper, we review the biological function of NBAS, NBAS gene mutation-related diseases and their pathogenesis in recent years.

     

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