No evidence for germ-line transmission following prenatal and early postnatal AAV-mediated gene delivery

2005 ◽  
Vol 7 (5) ◽  
pp. 630-637 ◽  
Author(s):  
Marcus Jakob ◽  
Christiane Mühle ◽  
Jung Park ◽  
Susi Weiß ◽  
Simon Waddington ◽  
...  
2004 ◽  
Vol 313 (3) ◽  
pp. 528-533 ◽  
Author(s):  
Alok S Pachori ◽  
Luis G Melo ◽  
Lunan Zhang ◽  
Massimo Loda ◽  
Richard E Pratt ◽  
...  

2006 ◽  
Vol 210 (S 5) ◽  
Author(s):  
M Jakob ◽  
C Mühle ◽  
J Park ◽  
S Frank ◽  
S Waddington ◽  
...  

2006 ◽  
Vol 210 (S 5) ◽  
Author(s):  
M Jakob ◽  
C Mühle ◽  
J Park ◽  
S Frank ◽  
S Waddington ◽  
...  

2006 ◽  
Vol 210 (S 5) ◽  
Author(s):  
M Jakob ◽  
C Mühle ◽  
J Park ◽  
S Frank ◽  
S Waddington ◽  
...  

1990 ◽  
Vol 10 (12) ◽  
pp. 6755-6758
Author(s):  
B R Stanton ◽  
S W Reid ◽  
L F Parada

We have disrupted one allele of the N-myc locus in mouse embryonic stem (ES) cells by using homologous recombination techniques and have obtained germ line transmission of null N-myc ES cell lines with transmission of the null N-myc allele to the offspring. The creation of mice with a deficient N-myc allele will allow the generation of offspring bearing null N-myc alleles in both chromosomes and permit study of the role that this proto-oncogene plays in embryonic development.


Development ◽  
1987 ◽  
Vol 99 (1) ◽  
pp. 15-23
Author(s):  
L.D. Etkin ◽  
B. Pearman

We analysed the fate, expression and germ line transmission of exogenous DNA which was microinjected into fertilized eggs of Xenopus laevis. DNA was injected into fertilized eggs within 1 h following fertilization. The injected DNA was dispersed around the site of injection and became localized to cleavage nuclei by stage 6. Injected DNA persisted in the tissues of 6- to 8-month-old frogs and exhibited a mosaic pattern of distribution with regard to the presence or absence and copy number between different tissues. We detected the exogenous DNA sequences in 60% of injected frogs. Restriction digestion analysis of this DNA suggested that it is not rearranged and was organized as head-to-tail multimers. The copy number varied from 2 to 30 copies/cell in various tissues of the same frog. Plasmid pSV2CAT which contains the prokaryotic gene coding for chloramphenicol acetyl transferase (CAT) enzyme linked to the SV40 early gene promoter was expressed in 50% of the animals containing the gene. The pattern of expression, however, varied between different animals and could not be correlated with copy number. We also showed that the exogenous DNA sequences were transmitted through the male germ line and that each offspring contained the gene integrated into a different region of the genome.


2008 ◽  
Vol 89 (5) ◽  
pp. 1448-1454 ◽  
Author(s):  
Yoshiyuki Kojima ◽  
Yutaro Hayashi ◽  
Satoshi Kurokawa ◽  
Kentaro Mizuno ◽  
Shoichi Sasaki ◽  
...  

1997 ◽  
Vol 209 (1) ◽  
pp. 85-91 ◽  
Author(s):  
Xin Liu ◽  
Hong Wu ◽  
Janet Loring ◽  
Sheriar Hormuzdi ◽  
Christine M. Disteche ◽  
...  

2005 ◽  
Vol 17 (2) ◽  
pp. 113 ◽  
Author(s):  
Poul Maddox-Hyttel ◽  
Jakob O. Gjørret

Current knowledge on the biology of mammalian embryonic stem cells (ESC) is stunningly sparse in light of their potential value in studies of development, functional genomics, generation of transgenic animals and human medicine. Despite many efforts to derive ESC from other mammalian species, ESC that retain their capacity for germ line transmission have only been verified in the mouse. However, the criterion of germ line transmission may not need to be fulfilled for exploitation of other abilities of these cells. Promising results with human ESC-like cells and adult stem cells have nourished great expectations for their potential use in regenerative medicine. However, such an application is far from reality and substantial research is required to elucidate aspects of the basic biology of pluripotent cells, as well as safety issues associated with the use of such cells in therapy. In this context, methods for the derivation, propagation and differentiation of ESC-like cultures from domestic animals would be highly desirable as biologically relevant models. Here, we review previously published efforts to establish bovine ESC-like cells and describe a procedure used in attempts to derive similar cells from bovine Day 12 embryos.


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