A chimaeric hygromycin resistance gene as a selectable marker in plant cells

1985 ◽  
Vol 5 (5) ◽  
pp. 299-302 ◽  
Author(s):  
Peter J. M. van den Elzen ◽  
Jeffrey Townsend ◽  
Kathleen Y. Lee ◽  
John R. Bedbrook
2000 ◽  
Vol 173 (3) ◽  
pp. 187-192 ◽  
Author(s):  
Akihiro Hara ◽  
Mitsuyoshi Ueda ◽  
Satoru Misawa ◽  
Toru Matsui ◽  
Keizo Furuhashi ◽  
...  

1991 ◽  
Vol 97 (2) ◽  
pp. 832-835 ◽  
Author(s):  
Zhenwei Zheng ◽  
Akio Hayashimoto ◽  
Zhijian Li ◽  
Norimoto Murai

1989 ◽  
Vol 9 (5) ◽  
pp. 1965-1968 ◽  
Author(s):  
T T Egelhoff ◽  
S S Brown ◽  
D J Manstein ◽  
J A Spudich

We have constructed an expression cartridge which has the bacterial hygromycin resistance gene (hph) fused to the Dictyostelium discoideum actin 15 promoter, with a segment of 3'-flanking DNA from the actin 15 locus placed downstream of the hph gene to serve as a transcription terminator. The plasmid pDE109, which contained this cartridge and a Dictyostelium origin of replication, transformed D. discoideum with high efficiency under hygromycin selection. The availability of this selectable marker circumvents the previous limitation of having G418 resistance as the only selectable marker for this organism; secondary transformation can now be used to introduce DNA into previously transformed cell lines.


Gene ◽  
1987 ◽  
Vol 57 (1) ◽  
pp. 21-26 ◽  
Author(s):  
D. Cullen ◽  
S.A. Leong ◽  
L.J. Wilson ◽  
D.J. Henner

2006 ◽  
Vol 154 (2) ◽  
pp. 187-193 ◽  
Author(s):  
Walid Hamada ◽  
Marie-Christine Soulié ◽  
Pierrette Malfatti ◽  
Gilbert Bompeix ◽  
Martine Boccara

Genetics ◽  
1998 ◽  
Vol 150 (4) ◽  
pp. 1459-1466 ◽  
Author(s):  
Chaozu He ◽  
Anca G Rusu ◽  
Agnieszka M Poplawski ◽  
John A G Irwin ◽  
John M Manners

Abstract Two biotypes (A and B) of Colletotrichum gloeosporioides infect the tropical legumes Stylosanthes spp. in Australia. These biotypes are asexual and vegetatively incompatible. However, field isolates of biotype B carrying a supernumerary 2-Mb chromosome, thought to originate from biotype A, have been reported previously. We tested the hypothesis that the 2-Mb chromosome could be transferred from biotype A to biotype B under laboratory conditions. Selectable marker genes conferring resistance to hygromycin and phleomycin were introduced into isolates of biotypes A and B, respectively. A transformant of biotype A, with the hygromycin resistance gene integrated on the 2-Mb chromosome, was cocultivated with phleomycin-resistant transformants of biotype B. Double antibiotic-resistant colonies were obtained from conidia of these mixed cultures at a frequency of approximately 10-7. Molecular analysis using RFLPs, RAPDs, and electrophoretic karyotypes showed that these colonies contained the 2-Mb chromosome in a biotype B genetic background. In contrast, no double antibiotic colonies developed from conidia obtained from mixed cultures of phleomycin-resistant transformants of biotype B with biotype A transformants carrying the hygromycin resistance gene integrated in chromosomes >2 Mb in size. The results demonstrated that the 2-Mb chromosome was selectively transferred from biotype A to biotype B. The horizontal transfer of specific chromosomes across vegetative incompatibility barriers may explain the origin of supernumerary chromosomes in fungi.


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