Relevance of BAC transgene copy number in mice: transgene copy number variation across multiple transgenic lines and correlations with transgene integrity and expression

被引:95
作者
Chandler, Kelly J.
Chandler, Ronald L.
Broeckelmann, Eva M.
Hou, Yue
Southard-Smith, E. Michelle
Mortlock, Douglas P.
机构
[1] Vanderbilt Univ, Sch Med, Dept Mol Physiol & Biophys, Ctr Human Genet Res, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Sch Med, Div Med Genet, Dept Med, Nashville, TN 37232 USA
关键词
D O I
10.1007/s00335-007-9056-y
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
Bacterial artificial chromosomes (BACs) are excellent tools for manipulating large DNA fragments and, as a result, are increasingly utilized to engineer transgenic mice by pronuclear injection. The demand for BAC transgenic mice underscores the need for careful inspection of BAC integrity and fidelity following transgenesis, which may be crucial for interpreting transgene function. Thus, it is imperative that reliable methods for assessing these parameters are available. However, there are limited data regarding whether BAC transgenes routinely integrate in the mouse genome as intact molecules, how BAC transgenes behave as they are passed through the germline across successive generations, and how variation in BAC transgene copy number relates to transgene expression. To address these questions, we used TaqMan real-time PCR to estimate BAC transgene copy number in BAC transgenic embryos and lines. Here we demonstrate the reproducibility of copy number quantification with this method and describe the variation in copy number across independent transgenic lines. In addition, polymorphic marker analysis suggests that the majority of BAC transgenic lines contain intact molecules. Notably, all lines containing multiple BAC copies also contain all BAC-specific markers. Three of 23 founders analyzed contained BAC transgenes integrated into more than one genomic location. Finally, we show increased BAC transgene copy number correlates with increased BAC transgene expression. In sum, our efforts have provided a reliable method for assaying BAC transgene integrity and fidelity, and data that should be useful for researchers using BACs as transgenic vectors.
引用
收藏
页码:693 / 708
页数:16
相关论文
共 23 条
[1]   Effect of transgene copy number on survival in the G93A SOD1 transgenic mouse model of ALS [J].
Alexander, GM ;
Erwin, KL ;
Byers, N ;
Deitch, JS ;
Augelli, BJ ;
Blankenhorn, EP ;
Heiman-Patterson, TD .
MOLECULAR BRAIN RESEARCH, 2004, 130 (1-2) :7-15
[2]   Real-time quantitative PCR-based system for determining transgene copy number in transgenic animals [J].
Ballester, M ;
Castelló, A ;
Ibáñez, E ;
Sánchez, A ;
Folch, JM .
BIOTECHNIQUES, 2004, 37 (04) :610-613
[3]  
Bishop JO, 1996, REPROD NUTR DEV, V36, P607
[4]  
BISHOP JO, 1989, MOL BIOL MED, V6, P283
[5]   HEDGEHOG AND BMP GENES ARE COEXPRESSED AT MANY DIVERSE SITES OF CELL-CELL INTERACTION IN THE MOUSE EMBRYO [J].
BITGOOD, MJ ;
MCMAHON, AP .
DEVELOPMENTAL BIOLOGY, 1995, 172 (01) :126-138
[6]   A simple method for the isolation of genomic DNA from mouse tail free of real-time PCR inhibitors [J].
Burkhart, CA ;
Norris, MD ;
Haber, M .
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS, 2002, 52 (02) :145-149
[7]   Bmp2 transcription in osteoblast progenitors is regulated by a distant 3′ enhancer located 156.3 kilobases from the promoter [J].
Chandler, Ronald L. ;
Chandler, Kelly J. ;
McFarland, Karen A. ;
Mortlock, Douglas P. .
MOLECULAR AND CELLULAR BIOLOGY, 2007, 27 (08) :2934-2951
[8]   Recombineering: A powerful new tool for mouse functional genomics [J].
Copeland, NG ;
Jenkins, NA ;
Court, DL .
NATURE REVIEWS GENETICS, 2001, 2 (10) :769-779
[9]   Distant regulatory elements in a Sox10-βGEO BAC transgene are required for expression of Sox10 in the enteric nervous system and other neural crest-derived tissues [J].
Deal, Karen K. ;
Cantrell, V. Ashley ;
Chandler, Ronald L. ;
Saunders, Thomas L. ;
Mortlock, Douglas P. ;
Southard-Smith, E. Michelle .
DEVELOPMENTAL DYNAMICS, 2006, 235 (05) :1413-1432
[10]  
DiLeone RJ, 1998, GENETICS, V148, P401