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双语推荐:锌指

乳腺癌转移的分子机制目前尚不完全清楚。近年研究发现锌指蛋白在肿瘤形成、生长以及转移中起着重要作用,现对锌指蛋白在乳腺癌转移过程中的作用进行综述。
The molecular mechanisms of breast cancer metastasis still remain unclear.Recent studies have found that zinc finger protein plays critical roles in determining tumor formation,occurrence,development and metastasis.This review summarized the functions of zinc finger protein in breast cancer metastasis.

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X染色体耦联锌指蛋白(Zfx)是锌指蛋白家族的一员,在多种干细胞和恶性肿瘤细胞中异常表达,研究表明其在干细胞的自我更新以及肿瘤细胞增殖、凋亡和迁移等方面发挥重要的作用.
Zinc-finger protein X-linked is a member of zinc finger protein family.Its abnormal expression has been found in a variety of stem cells and malignant tumor cells.Recent studies have shown that it plays an important role in stem cell self-renewal and cancer cell proliferation,apoptosis and migration.

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锌指蛋白在原核生物与真核生物基因转录的调控中发挥着重要作用.根据火龙果抗逆cDNA芯片中的一个EST设计一对引物,采用RT-PCR克隆火龙果类锌指蛋白基因片段,生物信息学分析表明,该片段长334bp,编码1中含有109个氨基酸残基的肽链,命名为HuZF.该基因序列与其它植物锌指蛋白基因核苷酸序列的同源性均在70%以上,推测的氨基酸序列与其它植物锌指蛋白的氨基酸序列的同源性达60%以上.RT-PCR分析表明,高盐和干旱胁迫下,火龙果茎中HuZF的表达增强,低温胁迫时,HuZF的表达先减弱后增强,初步推测该基因的表达与火龙果低温、高盐、干旱等逆境胁迫响应相关.
Zinc finger proteins play important roles in regulating gene expression in both prokaryotes and eukaryotes .In the presnt study ,a pair of primers was designed based on EST from cDNA microarray of pitaya (Hylocereus undulatus Britt) ,and a zinc finger protein gene fragment was cloned by reverse tran-scription-polymerase chain reaction (RT-PCR) .Bioinformatics analysis showed that the zinc finger protein gene fragment contained 334 bp nucleotide acids ,encoding a peptide chain of 109 amino acids ,and was designated as H uZF .Homology comparison with the sequences of zinc finger protein genes from other plants showed that they shared over 70% nucleotide sequence and over 60% amino acid sequence .RT-PCR analysis demonstrated that the expression of H uZF was up-regulated as exposed to high salt and drought stress ,and first down-regulated and then up-regulated under cold stress .It is tentatively speculated that the expression of H uZF is associated with the response of the plant

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目的 探讨皮肤鳞状细胞癌(皮肤鳞癌)组织中锌指蛋白A20、核因子κB(NF-κB)的表达及其与人乳头状瘤病毒(HPV)感染的关系.方法 收集43例皮肤鳞状细胞癌和21例健康人皮肤组织,利用基因芯片法检测21种HPV亚型,免疫组化法检测锌指蛋白A20和NF-κB表达水平,分析临床病理特征及其与HPV感染的关系.结果 锌指蛋白A20、NF-κB的表达水平在皮肤鳞癌患者不同年龄、性别、肿瘤原发部位和组织学分级组间差异均无统计学意义(P>0.05);皮肤鳞癌临床不同分期组间锌指蛋白A20、NF-κB的表达水平(Ⅰ+Ⅱ级组39例和Ⅲ级组4例锌指蛋白A20分别为25.85±3.84和48.34±7.69,NF-κB分别为46.64±8.93和57.34±10.02)以及有无淋巴结转移组间(有转移组3例和无转移组40例锌指蛋白A20分别为35.34±6.02和26.51±4.09,NF-κB分别为57.53±13.32和45.45±9.64)差异均有统计学意义(P<0.05或<0.01).在低危型HPV、高危型HPV、高危型/低危型混合感染的皮肤鳞癌组织中,A20表达分别为8例中2例、13例中5例和3例中1例阳性,NF-κB p65表达分别为3、10和2例阳性,经Fisher精确概率法计算,NF-κB p65与A20在3组中表达的阳性率差异均无统计学意义(P>0.05).HPV感染的鳞癌组织中锌指蛋白A20和NF-κBp65染色积分呈
Objective To measure the expressions of zinc finger protein A20 and nuclear factor (NF)-κB in cutaneous squamous cell carcinoma (CSCC) tissue and their correlation with human papillomavirus (HPV) infection.Methods Tissue specimens were obtained from the lesions of 43 patients with CSCC and normal skin of 21 healthy human controls.Gene chips were used to detect the DNA of 21 HPV subtypes in these specimens.The expression levels of zinc finger protein A20 and NF-κB were determined by immunohistochemistry.The correlation between clinicopathological features of CSCC and HPV infection was estimated by Spearman rank correlation analysis.Results No significant difference was found in the expression level of either zinc finger protein A20 or NF-κB among patients of different age groups,gender,and with CSCC of different primary sites or histological grade (all P > 0.05).However,there was a significant difference in the expression levels of zinc finger protein A20 and NF-κB betwee

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锌指蛋白是一类重要的转录因子,在植物应对外界生物和非生物胁迫的过程中起着极为重要的调节作用。基于二倍体雷蒙德氏棉基因组数据库,本研究从抗枯萎病、耐黄萎病的转基因抗虫棉品种鲁棉研32号中克隆到棉花锌指蛋白类基因Gh CHP。序列分析表明,Gh CHP基因的开放阅读框长度为720 bp,编码239个氨基酸,预测的蛋白质等电点为9.12。通过与其它植物锌指蛋白的序列进行聚类和比对分析,发现Gh CHP与拟南芥的AT2g16050和小麦的Ta CHP极为相近,其中两个保守的C1结构域呈典型的锌指结构。实时荧光定量PCR检测表明,Gh CHP在经过不同胁迫处理的棉花根和叶中的表达模式存在差异。PEG、Na Cl、H2O2、低温和黄萎病菌侵染处理均对Gh CHP的表达产生较大影响,表明Gh CHP可能在棉花生物和非生物胁迫响应中起重要的调控作用,是棉花品种抗逆性分子改良的重要候选基因。
Zinc finger proteins are important regulatory factors involving in plant responses to biotic and abiotic stresses. Based on genomic sequences of diploid cotton Gossypium raimondii, we cloned a new cotton zinc finger gene GhCHP from Lumianyan32, a transgenic Bt upland cotton variety characterized by Fusarium wilt resistance and Verticillium wilt tolerance. Sequence analysis revealed that the open reading frame is 720 bp by length, encoding a protein of 239 amino acids with an estimated isoelectric point of 9.12. Compared to other zinc finger protein sequences, GhCHP shows highest similarity to AT2g16050 in A rabidopsis thaliana and TaCHP in Triticum aestivum, with two highly conserved C1 domain. Further analysis by real time quantitative PCR demonstrated that the expression patterns of GhCHP in cotton leaves and roots were different under stress conditions such as PEG, NaCl, H2O2, low temperature and the defoliating Verticillium strain VD8, respectively, suggesting that GhCHP

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旨在原核表达Pokemon基因的锌指结构域,纯化获得GST-Zinc finger的融合蛋白。以人胶质瘤T98G细胞的cDNA为模板,利用PCR扩增带有BamH I和Sal I酶切位点的人Pokemon基因的锌指结构域,然后将其克隆到pGEX-4T-1原核表达载体中。将正确的重组载体转入大肠杆菌BL21(DE3),用IPTG诱导表达,再利用MagneGST particles亲和纯化Zinc finger融合蛋白,最后通过Western blot鉴定此融合蛋白。结果显示,成功构建pGEX-4T-1-Zinc finger原核表达载体;30℃条件下,0.2 mmol/L的IPTG能诱导出大量的可溶性GST-Zinc finger蛋白;经MagneGST particles纯化的GST-Zinc finger蛋白可被识别Pokemon锌指结构域的抗体特异识别。纯化的GST-Zinc finger蛋白可用于后续的生物学研究。
It was to express human Zinc finger domain of Pokemon gene in prokaryotic cells and purify the GST-Zinc finger fusion protein. The segment of zinc finger domain of Pokemon gene was amplified by PCR and cloned into prokaryotic expression vector pGEX-4T-1. The recombinant plasmid pGEX-4T-1-Zinc finger was transformed into E.coli BL21(DE3)and exogenous protein was induced by IPTG. After purification using MagneGST particles, the GST-Zinc finger fusion protein was further identified by Western blot. Results showed that the recombinant plasmid pGEX-4T-1-Zinc finger was constructed successfully. When BL21(DE3)cells transformed with pGEX-4T-1-Zinc finger were cultured at 30℃and induced with 0.2 mmol/L IPTG, GST-Zinc finger protein was obtained in a large quantity in supernatant. The purified GST-Zinc finger was further identified specifically by Pokemon antibody. Therefore, it proved that GST-Zinc finger fusion protein was successfully expressed and purified, and could be used for

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CCCH型锌指蛋白是一类生物体中广泛存在的转录因子,与植物的抗逆性密切相关。水稻CCCH锌指蛋白家族包括67个成员,分为8个亚家族。本研究采用实时定量PCR技术分析水稻CCCH亚家族Ⅰ基因的组织表达模式以及盐、干旱、低温、高温等多种非生物胁迫和脱落酸( ABA)对CCCH基因表达水平的调节。结果表明,多数 CCCH 基因都不同程度地受到这些非生物胁迫及 ABA 的诱导或抑制,其中 C3H10、C3H24、C3H33、C3H37和C3H67的表达量在不同胁迫处理后表现出不同程度的升高,C3H35、C3H50和C3H52在盐、干旱、ABA、低温和高温处理后表达水平呈下降趋势,表明这些CCCH锌指蛋白可能参与水稻的非生物胁迫响应。
CCCH-type zinc finger proteins , a kind of widely distributed transcription factors , are close-ly related to plant tolerance to stress .CCCH-type zinc finger protein family in rice contains 67 members, which are devided into 8 subfamilies .The tissue-specific expression patterns of CCCH -zinc finger protein subfamily Ⅰgenes and the adjustment of ABA and abiotic stresses such as salt , drought , low and hight tem-perature to CCCH genes expression level were analyzed by real time PCR .The results showed that most of CCCH genes were induced or restrained by the abiotic stresses and ABA at varying degrees .The expression quantities of C3H10, C3H24, C3H33, C3H37 and C3H67 genes were up-regulated, while those of C3H35, C3H50 and C3H52 genes were declining .It indicated that CCCH subfamily Ⅰgenes might be involved in re-sponse to abiotic stress .

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植物中C3HC4型RING锌指蛋白在泛素化、光形态建成、抗逆及生长发育等过程中均起到非常重要的作用。首次从本生烟中扩增获得一个锌指蛋白基因的完整阅读框,编码203个氨基酸,含有C3HC4型锌指结构域,命名为NbZFP1。将NbZFP1基因分别克隆到原核表达系统载体pGEX-6P-2以及pMAL-C2X中,成功构建了重组表达载体pGEX-6P-2-NbZFP1与pMALC2X-NbZFP1,经IPTG获得了大量可溶性表达的NbZFP1融合蛋白。将NbZFP1基因克隆于植物表达载体pBI121中,通过农杆菌介导法获得转基因烟草,PCR检测及Southern blot分析表明NbZFP1基因已整合到烟草基因组中,转NbZFP1基因烟草表现出株型紧凑,节间缩短,茎干粗壮和对TMV抗性增强。
C3HC4-type RING finger genes comprise a large family in the plant kingdom and play important roles in various physiologic processes of plant life. In this study, a zinc finger gene was isolated from Nicotiana benthamiana. Sequence analysis indicated that the gene encodes a 24 kD protein with 203 amino acids and contains one typical C3HC4 zinc finger domain and named NbZFP1. The entire coding region of NbZFP1 gene was then cloned into the bacterial expression vectors pGEX-6P-2 and pMAL-C2X. After IPTG induction, the recombinant protein was analyzed by SDS-PAGE, which showed that the expected protein was expressed at a high level in bacterial cells. NbZFP1 gene was cloned into the over-expression vector pBI121, and then transfered into Nicotiana benthamiana through Agrobacterium tumefacien-mediated transformation. According to PCR and Southern blot detection, NbZFP1 gene was successfully integrated into Nicotiana benthamiana genome. Regeneration plants showed type compactness, internode

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基因转录调节是植物对非生物胁迫适应机制的一个重要方面,转录调节因子在胁迫信号转导途径中调节下游基因的表达,在建立植物对胁迫适应性过程中起到重要作用.锌指蛋白是功能多样的转录调节因子蛋白家族,家族成员在植物响应非生物胁迫方面扮演着重要角色.本研究以秋茄C2H2型锌指蛋白编码基因KcZFP为目的基因,在烟草中过表达KcZFP,分析C2H2型锌指蛋白在植物耐盐性中的作用.研究结果显示:转基因株系中,KcZFP表达量显著提高.过表达KcZFP的烟草植株的耐盐性明显提高,在200 mmol/L NaCl处理的条件下,KcZFP过表达烟草中脯氨酸水平远高于野生型植株.对光合作用参数比较分析显示,在KcZFP过表达植株中净光合速率受盐胁迫的影响小于野生型植株,光合系统在一定程度上得到了保护.研究结果说明KcZFP作为转录调节因子参与了植物的渗透调节,对植物的耐盐性具有贡献.
Transcriptional regulation is one of the important factors in plant adaption to abiotic stress. In stress signaling pathway, transcription factors regulate downstream genes and play a critical role in the plant acclimation to adverse environments. Among transcription factors involved in abiotic stress response, zinc finger proteins represent a large protein family which displays diverse roles in various biological processes. In this study, the function of a KcZFP gene, encoding a Cys2/His2-type zinc-finger protein of Kandelia candel, was investigated in tobacco plants under salt treatment. The results showed that the transcript abundance of KcZFP was markedly elevated in transgenic plants. Salinity tolerance of KcZFP-transgenic plants was tested under 200 mmol/L NaCl. KcZFP-overexpressed tobacco plants exhibited an obviously higher salt tolerance than that of the wild type. The proline concentration in leaves of transgenic plants was markedly higher than that in wild-type under 200 mmo

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内质网氨肽酶1(ERAPl)及其异构体内质网氨肽酶2(ERAP2)都属于锌指金属基质肽酶M1家族中的“催产素酶亚家族”,共用GAMEN和HEXXH(X)18E锌结合基序.ERAPs在细胞内质网中参与内源性抗原肽的修饰及提呈,被认为是内质网中参与内源性抗原肽修饰的关键酶.近年来GWAS研究显示ERAPs与自身免疫性疾病相关,本文对ERAPs结构、功能及其相关疾病进行综述.
The ER aminopeptidase 1 (ERAP1) and the closely related ER aminopeptidase ERAP2,belong to the M1 family of zinc-metallopeptidase enzymes which share the consensus GAMEN and HEXXH (X) 18 E zincbinding motifs essential for enzymatic activity.ERAPs involved in endogenous antigen peptide processing and presentation in endoplasmic reticulum and was considered as key enzyme in endogenous peptides modification.Recent GWAS showed the association of ERAP1 and ERAP2 with several autoimmune diseases.In this review,we provide a general overview of ERAP1 and ERAP2 genes,their biological functions and their relevancy in related disease.