慢病毒載體用于轉(zhuǎn)基因技術(shù)的研究進展
本文關(guān)鍵詞:精子與慢病毒共孵育條件的優(yōu)化以及轉(zhuǎn)基因豬的制備,由筆耕文化傳播整理發(fā)布。
綜 述
慢病毒載體用于轉(zhuǎn)基因技術(shù)的研究進展 張曼,孫秀萍,宋銘晶
100021 北京,中國醫(yī)學(xué)科學(xué)院醫(yī)學(xué)實驗動物研究所 北京協(xié)和醫(yī)學(xué)院比較醫(yī)學(xué)中心 衛(wèi)生部人類疾病比較醫(yī)學(xué)重點實驗室宋銘晶,Email: songmj@cnilas.org
摘要:慢病毒載體作為目前研究最多的外源性轉(zhuǎn)基因載體之一,已成為一種高效率的轉(zhuǎn)基因和基因治療工具。該載體最大的優(yōu)勢是能夠感染分裂和靜止?fàn)顟B(tài)下的細(xì)胞,并且能夠高效、穩(wěn)定地整合于宿主細(xì)胞內(nèi)。目前研究該載體在多種動物轉(zhuǎn)基因技術(shù)方面的應(yīng)用,有助于我們利用除了大鼠和小鼠以外的多種實驗動物來研究基因的功能,并實現(xiàn)通過調(diào)節(jié)基因表達(dá)治療人類疾病的目的。
關(guān)鍵詞:病毒整合; 慢病毒載體; 宿主細(xì)胞; 基因治療
北京市自然科學(xué)基金(7122110);國家自然科學(xué)基金(31301890)
Research progress of using lentiviral vector to transgenic technology Zhang Man, Sun Xiuping, Song MingjingKey Laboratory of Human Diseases Comparative Medicine, Ministry of Health, Institute of Laboratory Animal Science, Chinese Academy of Medical Sciences & Comparative Medicine Centre, Peking Union MedicSong Mingjing, Email: songmj@cnilas.org
Abstract:Lentiviral vector, as one of the most studied exogenous transgenic vectors, has become an efficient tool to modify gene. The biggest advantage of lentiviral vector is its ability to infect the cell during cell division or in stationary state. Moreover, it can integrate in the host cell stably and efficiently. We aim to study the function of gene by using lentiviral vectors to obtain transgenic animals besides mice and rats, and to treat diseases by regulating gene expression.
Keywords:Virus integration; Lentiviral vector; Host cell; Gene therapy
字體
閱讀
參考文獻(xiàn)
[1] Pferifer A, Hofmann A. Lentiviral transgenesis[J]. Transgenic Research, 2004, 13: 513-522.
[2] Solaiman F, Zink MA, Xu G, et al. Modular retro-vector for transgenic and therapeutic use[J]. Molecular Reprod Develop, 2000, 56: 309-315.
[3] 李振宇, 徐開林. 慢病毒載體構(gòu)建及結(jié)構(gòu)優(yōu)化[J]. 國外醫(yī)學(xué): 分子生物學(xué)冊, 2002, 24(5): 310-314.
[4] Sun M, Jiang R, Sun L. Construction of B7x Gene Overexpression Lentiviral-based Vector[J]. Chem Res Chinese Universities, 2011, 27(4): 623-627.
[5] 賈俊雙, 肖高芳, 張晟, 等. 慢病毒載體法制備紅色熒光蛋白轉(zhuǎn)基因小鼠[J]. 中國比較醫(yī)學(xué)雜志, 2012, 20(2): 12-16.
[6] 周磊, 陳婕, 徐欣, 等. 利用重組慢病毒載體建立穩(wěn)定表達(dá)綠色熒光蛋白細(xì)胞系[J]. 中國臨床醫(yī)學(xué), 2009, 16(2): 305-308.
[7] 管潔, 王秀平, 鄧瑤, 等. 含分泌型螢光素酶和綠色熒光蛋白雙報告基因的慢病毒載體的制備與表達(dá)分析[J]. 生物技術(shù)通訊, 2011, 22(2): 199-202.
[8] 王麗嫻, 王東陽, 李星, 等. 攜帶三種報告基因慢病毒載體的構(gòu)建及其實驗研究[J]. 中國生物工程雜志, 2011, 31(12): 86-92.
[9] Sun X, Liu G, Wang Z. Over-expression of VEGF165 in the adipose tissue-derived stem cells via the lentiviral vector[J]. Chinese Medical Journal, 2011, 124(19): 3093-3097.
[10] 趙文晶, 楊振麗, 顧蓓, 等. 囊泡膜蛋白相關(guān)蛋白VAP33對小鼠樹突狀細(xì)胞肉瘤惡性行為的抑制作用[J]. 中國腫瘤臨床, 2012, 39(12): 817-821.
[11] 賴建明, 林建華, 林文平, 等. 豬TGF-β1基因重組慢病毒載體的及其在BMSCs中的表達(dá)[J]. 中國修復(fù)重建外科雜志, 2012, 26(7): 849-854.
[12] 石永乾, 何文騰, 周洋, 等. 慢病毒載體介導(dǎo)的綠色熒光蛋白轉(zhuǎn)基因標(biāo)記法研究豬嵌合體制作[J]. 中國生物工程雜志, 2012, 32(8): 68-74.
[13] 李秀梅, 尤玉琴, 劉光澤, 等. 慢病毒介導(dǎo)的綠色熒光蛋白轉(zhuǎn)基因小鼠的制備及鑒定[J]. 解放軍醫(yī)學(xué)雜志, 2011, 36(9): 964-966.
[14] Sasaki E, Suemizu H, Shimada A, et al. Generation of transgenic non-human primates with germlinetransmission[J]. Nature, 2009, 459(7246): 523-527.
[15] 汪立芹, 劉晨曦, 王靜, 等. 卵周隙內(nèi)注射慢病毒生產(chǎn)轉(zhuǎn)基因綿羊的方法[J]. 中國實驗動物學(xué)報, 2011, 19(1): 12-15.
[16] 馬嘯, 葉華虎, 杜小燕, 等. 慢病毒載體感染小鼠曲細(xì)精管的研究[J]. 實驗動物科學(xué), 2010, 27(1): 5-9.
[17] 蔡偉光, 習(xí)欠云, 肖敏, 等. 精子與慢病毒共孵育條件的優(yōu)化以及轉(zhuǎn)基因豬的制備[J]. 中國農(nóng)業(yè)科學(xué), 2013, 46(9): 1903-1914.
[18] Xue R, Gu J, Du S. Lentivirus-mediated RNA interference targeting the ObR gene in human breast cancer MCF--7cells in a nude mouse xenograft model[J]. Chinese Medical Journal, 2012, 125(9): 1563-1570.
[19] Gao N, Zhang X, Jiang R, et al. LentiVirus-mediated RNA Interference and Over-expression of CDK2AP1 cDNA Regulate CDK2AP1 expression in Human Lung cancer A549 cells[J]. Chem Res Chinese Universities, 2011, 27(3): 445-449.
[20] 戴少軍, 楊少兵, 劉成, 等. 下調(diào)TPH2重組慢病毒載體的構(gòu)建及鑒定[J]. 中華實驗外科雜志, 2012, 29(1): 129-131.
[21] Annoni A, Goudy K, Akbarpour M, et al. Immune responses in liver-directed lentiviral gene therapy[J]. Translational Research, 2013, 161(4): 230-240.
[22] 江飛, 袁華, 丁思陽, 等. E2F-1基因RNAi慢病毒載體的構(gòu)建與鑒定[J]. 口腔生物醫(yī)學(xué), 2011, 2(1): 17-21.
[23] Guang Y, Chen H, Jun C. Lentivirus-mediated shRNA interference targeting STAT3 inhibits human pancreatic cancer cell invasion[J]. World Journal of Gastroenterology, 2009, 15(30): 3757-3766.
[24] Lois C, Hong EJ, Pease S, et al. Germline and transmission and tissue-specific expression of trangenes delivered bylentiviralvectors[J]. Scinece, 2002, 295(5556): 868-872.
[25] Akhtar J, Wang Z, Zhang ZP, et al. Lentiviral-mediated RNA interference targeting stathmin 1 gene in human gastric cancer cells inhibits proliferation in vitro and tumor growth in vivo[J]. Journal of Translational Medicine, 2013, 11(1): 212.
[26] McGinley LM, McMhon J, Stocca A, et al. Mesenchymal Stem Cell Surival in the Infarted Heart is Enhanced by Lentivirus Vector-mediated Hsp27 Expression[J]. Human Gene Therapy, 2013, 9(10): 1089.
[27] Zhao B, Yang C, Yang S, et al. Construction of conditional lentivirus-mediated shRNA vector targeting the human Mirk gene and identification of RNAi efficiency in rhabdomyosarcoma RD cells[J]. International Journal of Oncology, 2013, 43(9): 1253-1259.
[28] Le Provost F, Lillico S, Passet B, et al. Zinc finger nuclease technology heralds a new rea in mammalian transgenesis[J]. CELL, 2010, 28(3): 134-141.
[29] 劉曉, 方永志, 劉文浩, 等. 鋅指核酸酶技術(shù)在動物轉(zhuǎn)基因研究中的應(yīng)用[J]. 山東農(nóng)業(yè)科學(xué), 2013, 45(2): 135-138.
[30] 王曉靜, 武建明, 王洪梅, 等. 鋅指核酸酶技術(shù)研究進展[J]. 家畜生態(tài)學(xué)報, 2011, 32(1): 1-4.
[31] Gabriel R, Lombardo A, Arens A, et al. An unbiased genome-wide analisis of zinc-finger nuclease specificity[J]. Nature Biotechnology, 2011, 29(9): 816-823.
[32] Janka M, Marinee KL, Thierry Vanden D. Recent Advances in Lentiviral Vector Decelopment and Applications[J]. Molecular Therapy, 2010, 18(3): 477-490.
[33] Torres R, Garcia A, Jinenez M, et al. An integration-defective lentivirus-based resourse for site-specific targeting of an edited safe-harbor locus in the human genome[J]. Gene Therpy, 2014, 21(4): 343-352.
[34] 周金偉, 王靈慧, 申義君, 等. 類轉(zhuǎn)錄激活因子效應(yīng)物核酸酶(TALENs)的構(gòu)建及其在基因組定點修飾中的應(yīng)用[J]. 中國細(xì)胞生物學(xué)學(xué)報, 2013, 35(11): 1-9.
[35] 張金邁, 任兆瑞. TALENs: 一種新的基因定點修飾技術(shù)[J]. 生命科學(xué), 2013, 25(1): 126-132.
(編輯:戚紅丹 收稿日期:2014-03-19)
本文關(guān)鍵詞:精子與慢病毒共孵育條件的優(yōu)化以及轉(zhuǎn)基因豬的制備,由筆耕文化傳播整理發(fā)布。
,本文編號:202974
本文鏈接:http://sikaile.net/kejilunwen/jiyingongcheng/202974.html