Transposon Tagging in Setaria viridis

Author(s):  
Kazuhiro Kikuchi ◽  
Christine Shyu ◽  
Thomas P. Brutnell
2020 ◽  
Vol 318 ◽  
pp. 57-67
Author(s):  
Mehanathan Muthamilarasan ◽  
Roshan Kumar Singh ◽  
Bonthala Venkata Suresh ◽  
Sumi Rana ◽  
Priya Dulani ◽  
...  

Weed Science ◽  
1971 ◽  
Vol 19 (6) ◽  
pp. 701-705 ◽  
Author(s):  
R. J. Burr ◽  
G. F. Warren

Several herbicides were tested in the greenhouse on ivyleaf morningglory (Ipomoea hederacea(L.) Jacq.), green foxtail (Setaria viridis(L.) Beauv.), purple nutsedge (Cyperus rotundusL.), and quackgrass (Agropyron repens(L.) Beauv.) to determine the degree of enhancement in activity that could be obtained with an isoparaffinic oil carrier applied at 140 L/ha. The enhancement varied with the herbicide and with the species, ranging from 16-fold enhancement with 2-chloro-4-(ethylamino)-6-(isopropylamino)-s-triazine (atrazine) and 2-sec-butyl-4,6-dinitrophenol (dinoseb) on ivyleaf morningglory to no enhancement of atrazine activity on purple nutsedge and quackgrass or (2,4-dichlorophenoxy)acetic acid (2,4-D) activity on quackgrass and ivyleaf morningglory. An oil adjuvant was less effective in enhancing dinoseb and 3-(3,4-dichlorophenyl)-1-methoxy-1-methylurea (linuron) activity than was the isoparaffinic oil carrier. Also, the isoparaffinic oil carrier emulsified in water was less effective than the undiluted oil in enhancing dinoseb activity on green foxtail, even though equal volumes of the isoparaffinic oil were applied.


PLoS ONE ◽  
2011 ◽  
Vol 6 (5) ◽  
pp. e19726 ◽  
Author(s):  
Jianping Zhang ◽  
Houyuan Lu ◽  
Naiqin Wu ◽  
Xiaoyan Yang ◽  
Xianmin Diao

2010 ◽  
Vol 22 (8) ◽  
pp. 2537-2544 ◽  
Author(s):  
Thomas P. Brutnell ◽  
Lin Wang ◽  
Kerry Swartwood ◽  
Alexander Goldschmidt ◽  
David Jackson ◽  
...  

2002 ◽  
Vol 06 (24) ◽  
pp. 930-935 ◽  
Author(s):  
Chang-deok Han

Transposable elements are powerful mutagens. Along with genomic sequences, knock-out phenotypes and expression patterns are important information to elucidate the function of genes. In this review, I propose a strategy to develop tranposant lines on a large scale by combining genetic cross and tissue culture of Ac and Ds lines. Based on the facts that Ds tends to be inactive in F2 or later generation and Ds becomes reactivated via tissue culture, a large scale of transposants can be produced by tissue culture of seeds carrying Ac and inactive Ds. In this review, I describe limitations and considerations in operating transposon tagging systems in rice. Also, I discuss the efficiency of our gene trap system and technical procedures to clone Ds flanking DNA.


Author(s):  
Polyana Kelly Martins ◽  
Bárbara Andrade Dias Brito da Cunha ◽  
Adilson Kenji Kobayshi ◽  
Hugo Bruno Correa Molinari

Author(s):  
Stephen L. Dellaporta ◽  
Irwin Greenblatt ◽  
Jerry L. Kermicle ◽  
James B. Hicks ◽  
Susan R. Wessler

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