Fertile homozygous transgenic mice expressing a functional truncated Herpes simplex thymidine kinase ΔTK gene

被引:26
作者
Cohen, JL
Boyer, O
Salomon, B
Onclercq, R
Depetris, D
Lejeune, L
Dubus-Bonnet, V
Bruel, S
Charlotte, F
Mattéï, MG
Klatzmann, D
机构
[1] Grp Hosp Pitie Salpetriere, Lab Biol & Therapeut Pathol Immunitaires, CNRS, ESA 7087, F-75013 Paris, France
[2] Grp Hosp Pitie Salpetriere, Lab Immunol B, F-75013 Paris, France
[3] Grp Hosp Pitie Salpetriere, Serv Anat Pathol, F-75013 Paris, France
[4] Genopoiet SARL, F-75013 Paris, France
[5] Fac Med Marseille, Lab Genet Med & Dev, INSERM, U406, F-13005 Marseille, France
关键词
thymidine kinase; ganciclovir; transgenic mice; lymphocyte depletion; human Herpesvirus I; male infertility;
D O I
10.1023/A:1008893206208
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Dividing cells expressing the Herpes simplex type 1 thymidine kinase (TK) can be killed upon ganciclovir treatment. Likewise, conditional cell knock-out can be: obtained in transgenic mice expressing a TK gene placed under the control of tissue-specific regulatory sequences. Such animals provide powerful experimental systems for assessing the functional role of specific cell populations through their time-controlled ablation. However, whatever the regulatory sequences used, a leaky toxic overexpression of TK in testis renders male TK-transgenic mice sterile and prevents the generation of homozygous TK-expressing animals. To solve this problem, we designed a truncated TK variant (Delta TK) not expressed in the testis. We generated transgenic mice expressing Delta TK under the control of lymphocyte-specific regulatory sequences derived from the CD4 gene. The Delta TK protein expressed in T-lymphocytes allowed the conditional ablation of activated T-cells in vitro and in vivo. Importantly, for one transgenic line we could generate fertile homozygous mice harboring a functional Delta TK transgene. Delta TK should thus dramatically facilitate the development of transgenic mice expressing a conditional suicide gene.
引用
收藏
页码:321 / 330
页数:10
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