• 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

Cabeza是一种编码新型RNA结合蛋白的果蝇基因,与EWS和TLS具有同源性,这两个基因与人肉瘤形成有关。

Cabeza, a Drosophila gene encoding a novel RNA binding protein, shares homology with EWS and TLS, two genes involved in human sarcoma formation.

作者信息

Stolow D T, Haynes S R

机构信息

Laboratory of Molecular Genetics, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Nucleic Acids Res. 1995 Mar 11;23(5):835-43. doi: 10.1093/nar/23.5.835.

DOI:10.1093/nar/23.5.835
PMID:7708500
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC306767/
Abstract

We have previously described a partial Drosophila cDNA, clone P19, which bears homology to members of the RNA recognition motif (RRM) family of proteins [Haynes et al. (1987) Proc. Natl. Acad. Sci. USA, 84, 1819-1823]. RNA binding as well as involvement in RNA processing has been demonstrated for some RRM proteins. We report here the further characterization of P19, which we renamed cabeza (caz). caz is located on the X chromosome at position 14B. Using Northern analysis, at least four transcripts from the caz gene were observed at varying levels during development. caz mRNA and protein are enriched in the brain and central nervous system during embryogenesis. In addition, the protein is enriched in the adult head. UV crosslinking was used to demonstrate in vitro RNA binding activity for full-length recombinant caz protein and for the caz RRM domain. Sequence analysis revealed caz is related to two human genes, EWS and TLS, which are involved in chromosomal translocations. The fusion of EWS and TLS to other cellular genes results in sarcoma formation. In addition to their overall structural organization and sequence similarity, these three genes share an RRM which is divergent from typical RRMs. Therefore, it appears that these genes constitute a new sub-family of RNA binding proteins.

摘要

我们之前描述过一个部分果蝇cDNA克隆P19,它与RNA识别基序(RRM)蛋白家族成员具有同源性[海恩斯等人(1987年),《美国国家科学院院刊》,84卷,1819 - 1823页]。一些RRM蛋白已被证明具有RNA结合以及参与RNA加工的功能。我们在此报告对P19的进一步特性描述,我们将其重新命名为cabeza(caz)。caz位于X染色体上14B位置。通过Northern分析,在发育过程中观察到来自caz基因的至少四种转录本,其水平各不相同。在胚胎发生过程中,caz mRNA和蛋白在脑和中枢神经系统中富集。此外,该蛋白在成虫头部也有富集。利用紫外线交联法证明了全长重组caz蛋白和caz RRM结构域具有体外RNA结合活性。序列分析表明caz与两个人类基因EWS和TLS相关,这两个基因参与染色体易位。EWS和TLS与其他细胞基因的融合会导致肉瘤形成。除了它们的整体结构组织和序列相似性外,这三个基因还共享一个与典型RRM不同的RRM。因此,这些基因似乎构成了一个新的RNA结合蛋白亚家族。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f11/306767/52b843700c42/nar00005-0127-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f11/306767/9ebc8d9f49a9/nar00005-0124-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f11/306767/606e1289a11c/nar00005-0125-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f11/306767/23f1abdde8cd/nar00005-0126-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f11/306767/bc6402d9c253/nar00005-0126-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f11/306767/85d7e55e138d/nar00005-0126-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f11/306767/52b843700c42/nar00005-0127-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f11/306767/9ebc8d9f49a9/nar00005-0124-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f11/306767/606e1289a11c/nar00005-0125-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f11/306767/23f1abdde8cd/nar00005-0126-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f11/306767/bc6402d9c253/nar00005-0126-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f11/306767/85d7e55e138d/nar00005-0126-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f11/306767/52b843700c42/nar00005-0127-a.jpg

相似文献

1
Cabeza, a Drosophila gene encoding a novel RNA binding protein, shares homology with EWS and TLS, two genes involved in human sarcoma formation.Cabeza是一种编码新型RNA结合蛋白的果蝇基因,与EWS和TLS具有同源性,这两个基因与人肉瘤形成有关。
Nucleic Acids Res. 1995 Mar 11;23(5):835-43. doi: 10.1093/nar/23.5.835.
2
Association of SARFH (sarcoma-associated RNA-binding fly homolog) with regions of chromatin transcribed by RNA polymerase II.肉瘤相关RNA结合果蝇同源物(SARFH)与RNA聚合酶II转录的染色质区域的关联。
Mol Cell Biol. 1995 Aug;15(8):4562-71. doi: 10.1128/MCB.15.8.4562.
3
Cloning and mapping of a human RBP56 gene encoding a putative RNA binding protein similar to FUS/TLS and EWS proteins.编码一种类似于FUS/TLS和EWS蛋白的假定RNA结合蛋白的人类RBP56基因的克隆与定位。
Genomics. 1996 Nov 15;38(1):51-7. doi: 10.1006/geno.1996.0591.
4
Fusion of CHOP to a novel RNA-binding protein in human myxoid liposarcoma.在人类黏液样脂肪肉瘤中CHOP与一种新型RNA结合蛋白的融合。
Nature. 1993 Jun 17;363(6430):640-4. doi: 10.1038/363640a0.
5
TLS/FUS fusion domain of TLS/FUS-erg chimeric protein resulting from the t(16;21) chromosomal translocation in human myeloid leukemia functions as a transcriptional activation domain.人髓系白血病中t(16;21)染色体易位产生的TLS/FUS-erg嵌合蛋白的TLS/FUS融合结构域具有转录激活结构域的功能。
Oncogene. 1994 Dec;9(12):3717-29.
6
A variant Ewing's sarcoma translocation (7;22) fuses the EWS gene to the ETS gene ETV1.一种变异型尤因肉瘤易位(7;22)将EWS基因与ETS基因ETV1融合。
Oncogene. 1995 Mar 16;10(6):1229-34.
7
Molecular cloning and subcellular localisation of the snRNP-associated protein 69KD, a structural homologue of the proto-oncoproteins TLS and EWS with RNA and DNA-binding properties.snRNP相关蛋白69KD的分子克隆与亚细胞定位,该蛋白是原癌蛋白TLS和EWS的结构同源物,具有RNA和DNA结合特性。
J Mol Biol. 1996 Dec 20;264(5):843-51. doi: 10.1006/jmbi.1996.0681.
8
A novel effector domain from the RNA-binding protein TLS or EWS is required for oncogenic transformation by CHOP.RNA结合蛋白TLS或EWS的一个新效应结构域是CHOP致癌转化所必需的。
Genes Dev. 1994 Nov 1;8(21):2513-26. doi: 10.1101/gad.8.21.2513.
9
Genomic structure of the human RBP56/hTAFII68 and FUS/TLS genes.人类RBP56/hTAFII68和FUS/TLS基因的基因组结构。
Gene. 1998 Oct 23;221(2):191-8. doi: 10.1016/s0378-1119(98)00463-6.
10
Expression patterns of the human sarcoma-associated genes FUS and EWS and the genomic structure of FUS.人类肉瘤相关基因FUS和EWS的表达模式以及FUS的基因组结构。
Genomics. 1996 Oct 1;37(1):1-8. doi: 10.1006/geno.1996.0513.

引用本文的文献

1
Understanding Amyotrophic Lateral Sclerosis: Pathophysiology, Diagnosis, and Therapeutic Advances.了解肌萎缩侧索硬化症:病理生理学、诊断和治疗进展。
Int J Mol Sci. 2024 Sep 15;25(18):9966. doi: 10.3390/ijms25189966.
2
Mitochondria Dysfunction in Frontotemporal Dementia/Amyotrophic Lateral Sclerosis: Lessons From Models.额颞叶痴呆/肌萎缩侧索硬化中的线粒体功能障碍:来自模型的经验教训
Front Neurosci. 2021 Nov 24;15:786076. doi: 10.3389/fnins.2021.786076. eCollection 2021.
3
Nearly 30 Years of Animal Models to Study Amyotrophic Lateral Sclerosis: A Historical Overview and Future Perspectives.

本文引用的文献

1
Ewing sarcoma 11;22 translocation produces a chimeric transcription factor that requires the DNA-binding domain encoded by FLI1 for transformation.尤因肉瘤11号与22号染色体易位产生一种嵌合转录因子,该因子转化需要由FLI1编码的DNA结合结构域。
Proc Natl Acad Sci U S A. 1993 Jun 15;90(12):5752-6. doi: 10.1073/pnas.90.12.5752.
2
Fusion of CHOP to a novel RNA-binding protein in human myxoid liposarcoma.在人类黏液样脂肪肉瘤中CHOP与一种新型RNA结合蛋白的融合。
Nature. 1993 Jun 17;363(6430):640-4. doi: 10.1038/363640a0.
3
Hel-N1: an autoimmune RNA-binding protein with specificity for 3' uridylate-rich untranslated regions of growth factor mRNAs.
近 30 年研究肌萎缩侧索硬化症的动物模型:历史回顾与未来展望。
Int J Mol Sci. 2021 Nov 12;22(22):12236. doi: 10.3390/ijms222212236.
4
Amyotrophic Lateral Sclerosis Genes in .肌萎缩侧索硬化症基因在...
Int J Mol Sci. 2021 Jan 18;22(2):904. doi: 10.3390/ijms22020904.
5
NPM-hMLF1 fusion protein suppresses defects of a Drosophila FTLD model expressing the human FUS gene.NPM-hMLF1 融合蛋白抑制表达人 FUS 基因的果蝇 FTLD 模型的缺陷。
Sci Rep. 2018 Jul 26;8(1):11291. doi: 10.1038/s41598-018-29716-9.
6
RNA-protein interactions in an unstructured context.非结构化环境中的 RNA-蛋白质相互作用。
FEBS Lett. 2018 Sep;592(17):2901-2916. doi: 10.1002/1873-3468.13116. Epub 2018 Jun 21.
7
FUS toxicity is rescued by the modulation of lncRNA hsrω expression in Drosophila melanogaster.FUS 毒性可通过调控果蝇长链非编码 RNA hsrω 的表达得到挽救。
Sci Rep. 2017 Nov 15;7(1):15660. doi: 10.1038/s41598-017-15944-y.
8
Role of FET proteins in neurodegenerative disorders.FET蛋白在神经退行性疾病中的作用。
RNA Biol. 2016 Nov;13(11):1089-1102. doi: 10.1080/15476286.2016.1211225. Epub 2016 Jul 14.
9
FUS-linked essential tremor associated with motor dysfunction in Drosophila.
Hum Genet. 2016 Nov;135(11):1223-1232. doi: 10.1007/s00439-016-1709-z. Epub 2016 Jul 9.
10
RGG boxes within the TET/FET family of RNA-binding proteins are functionally distinct.RNA结合蛋白TET/FET家族中的RGG框在功能上是不同的。
Transcription. 2016 Aug 7;7(4):141-51. doi: 10.1080/21541264.2016.1183071. Epub 2016 May 9.
Hel-N1:一种自身免疫性RNA结合蛋白,对生长因子mRNA富含3'尿苷酸的非翻译区具有特异性。
Mol Cell Biol. 1993 Jun;13(6):3494-504. doi: 10.1128/mcb.13.6.3494-3504.1993.
4
Zinc finger-like motifs in rat ribosomal proteins S27 and S29.大鼠核糖体蛋白S27和S29中的锌指样基序。
Nucleic Acids Res. 1993 Feb 11;21(3):649-55. doi: 10.1093/nar/21.3.649.
5
mRNA destabilization triggered by premature translational termination depends on at least three cis-acting sequence elements and one trans-acting factor.由过早翻译终止引发的信使核糖核酸(mRNA)不稳定取决于至少三个顺式作用序列元件和一个反式作用因子。
Genes Dev. 1993 Sep;7(9):1737-54. doi: 10.1101/gad.7.9.1737.
6
Analysis of the RNA-recognition motif and RS and RGG domains: conservation in metazoan pre-mRNA splicing factors.RNA识别基序以及RS和RGG结构域的分析:后生动物前体mRNA剪接因子中的保守性
Nucleic Acids Res. 1993 Dec 25;21(25):5803-16. doi: 10.1093/nar/21.25.5803.
7
Localized hedgehog activity controls spatial limits of wingless transcription in the Drosophila embryo.局部刺猬蛋白活性控制果蝇胚胎中无翅基因转录的空间界限。
Nature. 1993 Dec 9;366(6455):560-2. doi: 10.1038/366560a0.
8
Genetic and molecular analysis of the X chromosomal region 14B17-14C4 in Drosophila melanogaster: loss of function in NONA, a nuclear protein common to many cell types, results in specific physiological and behavioral defects.黑腹果蝇X染色体区域14B17 - 14C4的遗传与分子分析:多种细胞类型中常见的一种核蛋白NONA功能缺失,导致特定的生理和行为缺陷。
Genetics. 1993 Oct;135(2):419-42. doi: 10.1093/genetics/135.2.419.
9
Functional domains of the human splicing factor ASF/SF2.人类剪接因子ASF/SF2的功能结构域。
EMBO J. 1993 Dec;12(12):4727-37. doi: 10.1002/j.1460-2075.1993.tb06161.x.
10
Functional analysis of pre-mRNA splicing factor SF2/ASF structural domains.前体mRNA剪接因子SF2/ASF结构域的功能分析
EMBO J. 1993 Dec;12(12):4715-26. doi: 10.1002/j.1460-2075.1993.tb06160.x.