Chromosome engineering: prospects for gene therapy

被引:14
作者
Grimes, BR
Warburton, PE
Farr, CJ
机构
[1] Case Western Reserve Univ, Sch Med, Dept Genet, Cleveland, OH 44106 USA
[2] Univ Hosp Cleveland, Cleveland, OH 44106 USA
[3] CUNY Mt Sinai Sch Med, New York, NY 10029 USA
[4] Univ Cambridge, Dept Genet, Cambridge CB2 3EH, England
关键词
engineered chromosomes; gene therapy vector;
D O I
10.1038/sj.gt.3301763
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recent advances in chromosome engineering and the potential for downstream applications in gene therapy were presented at the Artificial Chromosome Session of Genome Medicine: Gene Therapy for the Millennium in Rome, Italy in September 2001. This session concentrated primarily on the structure and function of human centromeres and the ongoing challenge of equipping human artificial chromosomes (HACs) with centromeres to ensure their mitotic stability. Advances in the 'bottom up' construction of HACs included the transfer into HT1080 cells of circular PACs containing alpha satellite DNA, and the correction of HPRT deficiency in cells using HACs. Advances In the 'top down' construction of HACs using telomere associated chromosome fragmentation in DT40 cells included the formation of HACs that are less than a megabase in size and transfer of HACs through the mouse germline. Significant progress has also been made in the use of human minichromosomes for stable trans-gene expression. While many obstacles remain towards the use of HACs for gene therapy, this session provided an optimistic outlook for future success.
引用
收藏
页码:713 / 718
页数:6
相关论文
共 43 条
[1]   Molecular and cytological analysis of a 5.5 Mb minichromosome [J].
Auriche, C ;
Donini, P ;
Ascenzioni, F .
EMBO REPORTS, 2001, 2 (02) :102-107
[2]   Domain organization at the centromere and neocentromere [J].
Choo, KHA .
DEVELOPMENTAL CELL, 2001, 1 (02) :165-177
[3]   Engineering human chromosomes for gene therapy studies [J].
Choo, KHA .
TRENDS IN MOLECULAR MEDICINE, 2001, 7 (06) :235-237
[4]   Generation of transgenic mice and germline transmission of a mammalian artificial chromosome introduced into embryos by pronuclear microinjection [J].
Co, DO ;
Borowski, AH ;
Leung, JD ;
van der Kaa, J ;
Hengst, S ;
Platenburg, GJ ;
Pieper, FR ;
Perez, CF ;
Jirik, FR ;
Drayer, JI .
CHROMOSOME RESEARCH, 2000, 8 (03) :183-191
[5]  
Csonka E, 2000, J CELL SCI, V113, P3207
[6]   Efficient in-vitro transfer of a 60-Mb mammalian artificial chromosome into murine and hamster cells using cationic lipids and dendrimers [J].
de Jong, G ;
Telenius, A ;
Vanderbyl, S ;
Meitz, A ;
Drayer, J .
CHROMOSOME RESEARCH, 2001, 9 (06) :475-485
[7]   Mammalian artificial chromosome formation from circular alphoid input DNA does not require telomere repeats [J].
Ebersole, TA ;
Ross, A ;
Clark, E ;
McGill, N ;
Schindelhauer, D ;
Cooke, H ;
Grimes, B .
HUMAN MOLECULAR GENETICS, 2000, 9 (11) :1623-1631
[8]   FUNCTIONAL REINTRODUCTION OF HUMAN TELOMERES INTO MAMMALIAN-CELLS [J].
FARR, C ;
FANTES, J ;
GOODFELLOW, P ;
COOKE, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (16) :7006-7010
[9]   Making sense of eukaryotic DNA replication origins [J].
Gilbert, DM .
SCIENCE, 2001, 294 (5540) :96-100
[10]   Stable gene expression from a mammalian artificial chromosome [J].
Grimes, BR ;
Schindelhauer, D ;
McGill, NI ;
Ross, A ;
Ebersole, TA ;
Cooke, HJ .
EMBO REPORTS, 2001, 2 (10) :910-914