| Literature DB >> 10886776 |
J S Jeon1, S Lee, K H Jung, S H Jun, D H Jeong, J Lee, C Kim, S Jang, K Yang, J Nam, K An, M J Han, R J Sung, H S Choi, J H Yu, J H Choi, S Y Cho, S S Cha, S I Kim, G An.
Abstract
We have produced 22 090 primary transgenic rice plants that carry a T-DNA insertion, which has resulted in 18 358 fertile lines. Genomic DNA gel-blot and PCR analyses have shown that approximately 65% of the population contains more than one copy of the inserted T-DNA. Hygromycin resistance tests revealed that transgenic plants contain an average of 1.4 loci of T-DNA inserts. Therefore, it can be estimated that approximately 25 700 taggings have been generated. The binary vector used in the insertion contained the promoterless beta-glucuronidase (GUS) reporter gene with an intron and multiple splicing donors and acceptors immediately next to the right border. Therefore, this gene trap vector is able to detect a gene fusion between GUS and an endogenous gene, which is tagged by T-DNA. Histochemical GUS assays were carried out in the leaves and roots from 5353 lines, mature flowers from 7026 lines, and developing seeds from 1948 lines. The data revealed that 1.6-2.1% of tested organs were GUS-positive in the tested organs, and that their GUS expression patterns were organ- or tissue-specific or ubiquitous in all parts of the plant. The large population of T-DNA-tagged lines will be useful for identifying insertional mutants in various genes and for discovering new genes in rice.Entities:
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Year: 2000 PMID: 10886776 DOI: 10.1046/j.1365-313x.2000.00767.x
Source DB: PubMed Journal: Plant J ISSN: 0960-7412 Impact factor: 6.417