An iAc/Ds gene and enhancer trapping system for insertional mutagenesis in rice
Narayana M. Upadhyaya, Xue-Rong Zhou, Qian-Hao Zhu, Kerrie Ramm, Limin Wu, Andrew Eamens, Ramani Sivakumar, Tsuneo Kato, Dow-Won Yun, Chellian Santhoshkumar, Kottaram K. Narayanan, James W. Peacock and Elizabeth S. Dennis
Functional Plant Biology 29(5) 547 - 559
Abstract
We evaluated a two-component transposon iAc/Ds system
for generating a library of insertional mutants in rice. The constructs used
have gene or enhancer trapping properties, plasmid rescue and
T-DNA/Ds launching pad reporter facilities.
Mutagenic iAc/Ds lines were produced by three
methods: crossing iAc and Ds
containing lines; co-transformation with iAc and
Ds constructs; and super-transformation of
iAc transgenic calli with Ds
constructs. First and second generation screening populations, derived from
crosses (F2 and F3) or double
transformation (DtT1 and DtT2),
were analysed for stable insertion lines containing Ds
transposed to locations unlinked to iAc. The average
frequencies of putative stable insertion (PSI) lines in the
F2, DtT1,
F3 and DtT2 populations were 6.61,
5.58, 11.47 and 7.05% respectively, with large variations in these
frequencies in screening populations derived from different mutagenic lines.
Further analyses indicated that 41, 33, 65 and 64% of the PSI lines,
respectively, have Ds transposed to locations unlinked
to the original Ds launching pad. Using the plasmid
rescue system, sequences flanking Ds from 137 PSI lines
were obtained. Sixty-eight of these lines had unique insertions in genomic
regions, of which 18 were known sequences. Because the average frequency of
proven stable insertion lines in any of our screening populations has been
less than 5%, we suggest that additional features should be
incorporated in this two-component iAc/Ds system to
increase the screening efficiency, and to make it suitable for large-scale
insertional mutagenesis and determination of gene function in rice.
Full text doi:10.1071/PP01205
© CSIRO 2002





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