A structured mutant population for forward and reverse genetics in Barley (Hordeum vulgare L.)

被引:223
作者
Caldwell, DG
McCallum, N
Shaw, P
Muehlbauer, GJ
Marshall, DF
Waugh, R [1 ]
机构
[1] Scottish Crop Res Inst, Dundee DD2 5DA, Scotland
[2] Univ Minnesota, Dept Agron & Plant Genet, St Paul, MN 55108 USA
关键词
barley; ethylmethanesulfonate; Cel I; mutagenesis; reverse genetics;
D O I
10.1111/j.1365-313X.2004.02190.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Two large-scale ethylmethanesulfonate (EMS) mutant populations from barley (Hordeum vulgare L.) cv. Optic have been developed to promote both forward and reverse genetics in this crop. Leaf material and seed from approximately 20 000 M-2 plants were individually harvested, freeze-dried and archived. DNA was isolated from 9216 plants from the 20 and 30 mM EMS treatments and assembled into 1152 eight-plant pools. To facilitate PCR-based mutation scanning an approach has been employed that combines cleavage of heteroduplexes using the Cel nuclease (Cel I), post-cleavage intercalating dye labeling and the subsequent detection of cleaved products on a Transgenomic WAVE-HS. The populations were evaluated by screening for induced mutations in two genes of interest and the induced mutations were validated by sequence analysis. To enhance the screening process, 12-16 M-3 progeny from each of the M-2 plants were assessed for visible phenotypes and the data entered into a web accessible database (http://bioinf.scri.sari.ac.uk/distilling/distilling.html).
引用
收藏
页码:143 / 150
页数:8
相关论文
共 37 条
[21]   Transposon-mediated single-copy gene delivery leads to increased transgene expression stability in barley [J].
Koprek, T ;
Rangel, S ;
McElroy, D ;
Louwerse, JD ;
Williams-Carrier, RE ;
Lemaux, PG .
PLANT PHYSIOLOGY, 2001, 125 (03) :1354-1362
[22]   CEL I enzymatic mutation detection assay [J].
Kulinski, J ;
Besack, D ;
Oleykowski, CA ;
Godwin, AK ;
Yeung, AT .
BIOTECHNIQUES, 2000, 29 (01) :44-+
[23]   Deleteagene: a fast neutron deletion mutagenesis-based gene knockout system for plants [J].
Li, X ;
Lassner, M ;
Zhang, YL .
COMPARATIVE AND FUNCTIONAL GENOMICS, 2002, 3 (02) :158-160
[24]   A fast neutron deletion mutagenesis-based reverse genetics system for plants [J].
Li, X ;
Song, YJ ;
Century, K ;
Straight, S ;
Ronald, P ;
Dong, XN ;
Lassner, M ;
Zhang, YL .
PLANT JOURNAL, 2001, 27 (03) :235-242
[25]   Activation tagging using the En-I maize transposon system in Arabidopsis [J].
Marsch-Martinez, N ;
Greco, R ;
Van Arkel, G ;
Herrera-Estrella, L ;
Pereira, A .
PLANT PHYSIOLOGY, 2002, 129 (04) :1544-1556
[26]   Targeting induced local lesions in genomes (TILLING) for plant functional genomics [J].
McCallum, CM ;
Comai, L ;
Greene, EA ;
Henikoff, S .
PLANT PHYSIOLOGY, 2000, 123 (02) :439-442
[27]   Targeted screening for induced mutations [J].
McCallum, CM ;
Comai, L ;
Greene, EA ;
Henikoff, S .
NATURE BIOTECHNOLOGY, 2000, 18 (04) :455-457
[28]  
Nakagawa Y, 2000, PLANT CELL PHYSIOL, V41, P733, DOI 10.1093/pcp/41.6.733
[29]   Mutation detection using a novel plant endonuclease [J].
Oleykowski, CA ;
Mullins, CRB ;
Godwin, AK ;
Yeung, AT .
NUCLEIC ACIDS RESEARCH, 1998, 26 (20) :4597-4602
[30]   Control of leaf morphogenesis by microRNAs [J].
Palatnik, JF ;
Allen, E ;
Wu, XL ;
Schommer, C ;
Schwab, R ;
Carrington, JC ;
Weigel, D .
NATURE, 2003, 425 (6955) :257-263