• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

锌指蛋白 335 在大脑发育和免疫系统中的多面性。

The many faces of the zinc finger protein 335 in brain development and immune system.

机构信息

Key Laboratory of Molecular Medicine and Biotherapy, Department of Biology, School of Life Science, Beijing Institute of Technology, Beijing 100081, China.

出版信息

Biomed Pharmacother. 2023 Sep;165:115257. doi: 10.1016/j.biopha.2023.115257. Epub 2023 Aug 2.

DOI:10.1016/j.biopha.2023.115257
PMID:37541176
Abstract

Zinc finger protein 335 (ZNF335) plays a crucial role in the methylation and, consequently, regulates the expression of a specific set of genes. Variants of the ZNF335 gene have been identified as risk factors for microcephaly in a variety of populations worldwide. Meanwhile, ZNF335 has also been identified as an essential regulator of T-cell development. However, an in-depth understanding of the role of ZNF335 in brain development and T cell maturation is still lacking. In this review, we summarize current knowledge of the molecular mechanisms underlying the involvement of ZNF335 in neuronal and T cell development across a wide range of pre-clinical, post-mortem, ex vivo, in vivo, and clinical studies. We also review the current limitations regarding the study of the pathophysiological functions of ZNF335. Finally, we hypothesize a potential role for ZNF335 in brain disorders and discuss the rationale of targeting ZNF335 as a therapeutic strategy for preventing brain disorders.

摘要

锌指蛋白 335(ZNF335)在甲基化中发挥着关键作用,进而调控特定基因的表达。在全球范围内的各种人群中,ZNF335 基因的变异被鉴定为小头畸形的风险因素。同时,ZNF335 也被鉴定为 T 细胞发育的必需调节因子。然而,人们对 ZNF335 在大脑发育和 T 细胞成熟中的作用仍知之甚少。在这篇综述中,我们总结了 ZNF335 在神经和 T 细胞发育中涉及的分子机制的最新知识,这些知识来源于广泛的临床前、死后、离体、体内和临床研究。我们还回顾了目前研究 ZNF335 病理生理学功能的局限性。最后,我们假设 ZNF335 可能在脑疾病中发挥作用,并讨论了将 ZNF335 作为预防脑疾病的治疗策略的合理性。

相似文献

1
The many faces of the zinc finger protein 335 in brain development and immune system.锌指蛋白 335 在大脑发育和免疫系统中的多面性。
Biomed Pharmacother. 2023 Sep;165:115257. doi: 10.1016/j.biopha.2023.115257. Epub 2023 Aug 2.
2
Expanding the clinical spectrum of biallelic ZNF335 variants.扩大双等位基因 ZNF335 变异的临床谱。
Clin Genet. 2018 Aug;94(2):246-251. doi: 10.1111/cge.13260. Epub 2018 May 3.
3
Microcephaly gene links trithorax and REST/NRSF to control neural stem cell proliferation and differentiation.小头畸形基因将 trithorax 和 REST/NRSF 联系起来,以控制神经干细胞的增殖和分化。
Cell. 2012 Nov 21;151(5):1097-112. doi: 10.1016/j.cell.2012.10.043.
4
Association Between Invisible Basal Ganglia and ZNF335 Mutations: A Case Report.隐匿性基底神经节与ZNF335突变之间的关联:一例报告
Pediatrics. 2016 Sep;138(3). doi: 10.1542/peds.2016-0897. Epub 2016 Aug 18.
5
Novel biallelic ZNF335 variant causing primary microcephaly: A case report and radiological review.新发 ZNF335 双等位基因突变导致原发性小头畸形:病例报告及影像学复习。
Am J Med Genet A. 2024 Aug;194(8):e63593. doi: 10.1002/ajmg.a.63593. Epub 2024 Mar 28.
6
Primary and Secondary Microcephaly, Global Developmental Delay, and Seizure in Two Siblings Caused by a Novel Missense Variant in the ZNF335 Gene.一对兄妹患原发性和继发性小头畸形、全面发育迟缓伴癫痫,由 ZNF335 基因的一个新错义变异引起
J Mol Neurosci. 2022 Apr;72(4):719-729. doi: 10.1007/s12031-021-01955-y. Epub 2022 Jan 4.
7
mutations cause basal ganglia abnormality with progressive cerebral/cerebellar atrophy.突变导致基底节异常,并伴有进行性脑/小脑萎缩。
J Neurogenet. 2021 Mar;35(1):23-28. doi: 10.1080/01677063.2020.1833006. Epub 2020 Nov 20.
8
Molecular evolutionary analysis of human primary microcephaly genes.人类原发性小头畸形基因的分子进化分析。
BMC Ecol Evol. 2021 May 3;21(1):76. doi: 10.1186/s12862-021-01801-0.
9
Comprehensive review on the molecular genetics of autosomal recessive primary microcephaly (MCPH).常染色体隐性原发性小头畸形(MCPH)分子遗传学的综合综述。
Genet Res (Camb). 2018 Aug 8;100:e7. doi: 10.1017/S0016672318000046.
10
Molecular genetics of human primary microcephaly: an overview.人类原发性小头畸形的分子遗传学:综述
BMC Med Genomics. 2015;8 Suppl 1(Suppl 1):S4. doi: 10.1186/1755-8794-8-S1-S4. Epub 2015 Jan 15.

引用本文的文献

1
Advances in the Functionalization of Vaccine Delivery Systems: Innovative Strategies and Translational Perspectives.疫苗递送系统功能化的进展:创新策略与转化前景
Pharmaceutics. 2025 May 12;17(5):640. doi: 10.3390/pharmaceutics17050640.
2
Genes of the "regulation of lymphocyte activation" pathway may influence immune cells infiltration in growth hormone secreting pituitary tumors.“淋巴细胞激活调节”通路的基因可能影响生长激素分泌型垂体瘤中的免疫细胞浸润。
Pituitary. 2025 May 26;28(3):63. doi: 10.1007/s11102-025-01537-w.
3
The Human Accelerated Region HAR202 Controls NPAS3 Expression in the Developing Forebrain Displaying Differential Enhancer Activity Between Modern and Archaic Human Sequences.
人类加速区 HAR202 控制着发育中前脑的 NPAS3 表达,在现代人和古人类序列之间显示出不同的增强子活性。
Mol Biol Evol. 2024 Oct 4;41(10). doi: 10.1093/molbev/msae186.
4
Modulation of Adverse Health Effects of Environmental Cadmium Exposure by Zinc and Its Transporters.环境镉暴露的不良健康影响的锌及其转运体的调节。
Biomolecules. 2024 May 31;14(6):650. doi: 10.3390/biom14060650.