1986
DOI: 10.1128/mcb.6.12.4486
|View full text |Cite
|
Sign up to set email alerts
|

Isolation of tobacco DNA segments with plant promoter activity.

Abstract: We constructed a promoter probe vector, pGVL120, to isolate plant DNA segments with promoter activity in tobacco. Plant nuclear DNA Sau3A fragments were inserted in front of the npt-II sequence, and a mixture of recombinant plasmids was mobilized to Agrobacterium sp. and used to transform tobacco protoplasts. By kanamycin selection, transformed plant cell lines containing NPT-II T-DNAs were isolated. Eight of these cell lines were regenerated and analyzed for the levels of NPT-H activity in stem, root, midrib,… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

1
8
0

Year Published

1990
1990
2009
2009

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 19 publications
(9 citation statements)
references
References 31 publications
1
8
0
Order By: Relevance
“…This change makes this open reading frame identical to qacEAl. It should be noted that the open reading frame reported to be from A. tumefaciens (20) is not actually from this genus, but is located on an artificial cloning vector whose DNA derived originally from E. coli (23).…”
Section: Resultsmentioning
confidence: 99%
“…This change makes this open reading frame identical to qacEAl. It should be noted that the open reading frame reported to be from A. tumefaciens (20) is not actually from this genus, but is located on an artificial cloning vector whose DNA derived originally from E. coli (23).…”
Section: Resultsmentioning
confidence: 99%
“…The different promoter deletions were inserted as Barn HI/Bgl II fragments into the Bgl II site upstream of the promoterless NPTII gene of the intermediate Ti vector plasmid pGV180, a derivative of pGV150 [5,22].…”
Section: Methodsmentioning
confidence: 99%
“…These replicated T-DNAs might then preferentially integrate as an array into the plant genome. Until now, the main arguments supporting replication are that each of the T-DNAs involved in a direct or inverted repeat shows analogous breakpoints in a restriction analysis (Van Lijsebettens et al, 1986;Jorgensen et al, 1987) and that three identical T-DNA copies are present after transformation with a library of T-DNAs containing different promoters (Herman et al, 1986). In any case, the transferred singlestranded T-DNAs are made double stranded before integration (Chilton and Que, 2003) and self-replication of the newly synthesized strand might be an attractive explanation for the frequently observed inverted T-DNA repeats over the RB (Jorgensen et al, 1987).…”
Section: Introductionmentioning
confidence: 99%