Literature DB >> 3378672

Persistence and replication of plasmid DNA microinjected into early embryos of Xenopus laevis.

N J Marini1, L D Etkin, R M Benbow.   

Abstract

The persistence and replication of defined circular and linear plasmid DNA molecules microinjected into fertilized eggs of Xenopus laevis were analyzed. For all plasmids tested, a small fraction of microinjected circular molecules was replicated; however, the overall copy numbers of either free form I or form II molecules usually did not increase through blastulation. In contrast, extensive amplification of input DNA sequences was seen whenever the microinjected DNA was assembled into high molecular weight concatemers. Moreover, the appearance and subsequent replication of injected sequences in high molecular weight DNA were enhanced when linear (form III), rather than circular, molecules were microinjected. The injected form III DNA was rapidly converted into long linear concatemers. All possible orientations of monomeric molecules within the concatemers were observed although, on occasion, head-to-tail orientations were favored. Long linear concatemers were replicated very efficiently, irrespective of the sequence of the input DNA. Form I and form II DNA molecules were also formed in the embryo from microinjected form III DNA. A small fraction of these circular forms was replicated, although overall copy numbers did not increase significantly. Form III molecules that remained monomeric were not observed to be replicated at all within our limits of detection. In some batches of embryos, form I and form II DNA molecules were replicated to the extent that overall copy number increased. Even in these cases, however, the amplification of long linear concatemers of the input DNA sequences was more efficient.

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Year:  1988        PMID: 3378672     DOI: 10.1016/0012-1606(88)90328-4

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  24 in total

1.  A simplified method of generating transgenic Xenopus.

Authors:  D B Sparrow; B Latinkic; T J Mohun
Journal:  Nucleic Acids Res       Date:  2000-02-15       Impact factor: 16.971

2.  Undamaged DNA transmits and enhances DNA damage checkpoint signals in early embryos.

Authors:  Aimin Peng; Andrea L Lewellyn; James L Maller
Journal:  Mol Cell Biol       Date:  2007-07-30       Impact factor: 4.272

Review 3.  Transgenesis in fish.

Authors:  L M Houdebine; D Chourrout
Journal:  Experientia       Date:  1991-09-15

4.  The 5' untranslated region of mRNA for ribosomal protein S19 is involved in its translational regulation during Xenopus development.

Authors:  P Mariottini; F Amaldi
Journal:  Mol Cell Biol       Date:  1990-02       Impact factor: 4.272

5.  Differential compartmentalization of plasmid DNA microinjected into Xenopus laevis embryos relates to replication efficiency.

Authors:  N J Marini; R M Benbow
Journal:  Mol Cell Biol       Date:  1991-01       Impact factor: 4.272

Review 6.  Regulation and expression of transgenes in fish -- a review.

Authors:  A Iyengar; F Müller; N Maclean
Journal:  Transgenic Res       Date:  1996-05       Impact factor: 2.788

7.  Expression of exogenous DNA during the early development of the chick embryo.

Authors:  Margaret Perry; David Morrice; Simon Hettle; Helen Sang
Journal:  Rouxs Arch Dev Biol       Date:  1991-11

8.  Temporally uncontrolled expression of linearized plasmid DNA which carries bacterial chloramphenicol acetyltransferase gene withXenopus cardiacα-actin promoter after injection intoXenopus fertilized eggs.

Authors:  Koichiro Shiokawa; Yuchang Fu; Keiichi Hosokawa; K Yamana
Journal:  Rouxs Arch Dev Biol       Date:  1990-11

9.  Expression of circular and linearized bacterial chloramphenicol acetyltransferase genes with or without viral promoters after injection into fertilized eggs, unfertilized eggs and oocytes ofXenopus laevis.

Authors:  Yuchang Fu; Keiichi Hosokawa; Koichiro Shiokawa
Journal:  Rouxs Arch Dev Biol       Date:  1989-10

10.  Molecular analysis of transgenic plants generated by microprojectile bombardment: effect of petunia transformation booster sequence.

Authors:  C M Buising; R M Benbow
Journal:  Mol Gen Genet       Date:  1994-04
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