Home LiteratureArticle Details
PMID: 14617098 Published · ppublish English Journal Article

Sequence database of 1172 T-DNA insertion sites in Arabidopsis activation-tagging lines that showed phenotypes in T1 generation.

The Plant journal : for cell and molecular biology ·Vol. 36 ·No. 3 ·2003-11-00 ·Pages 421-9

Ichikawa T, Nakazawa M, Kawashima M, Muto S, Gohda K, Suzuki K, Ishikawa A, Kobayashi H, Yoshizumi T, Tsumoto Y, Tsuhara Y, Iizumi H, Goto Y, Matsui M

Abstract

Plant genomic resources harbouring gain-of-function mutations remain rare, even though this type of mutation is believed to be one of the most useful for elucidating the function of unknown genes that have redundant partners in the genome. An activation-tagging T-DNA was introduced into the genome of Arabidopsis creating 55,431 independent transformed lines. Of these T1 lines, 1,262 showed phenotypes different from those of wild-type plants. We called these lines 'AT1Ps' (activation T1 putants). The phenotypes observed include abnormalities in morphology, growth rate, plant colour, flowering time and fertility. Similar phenotypes re-appeared either in dominant or semi-dominant fashion in 17% of 177 AT2P plants tested. Plasmid rescue or an adaptor-PCR method was used to identify 1172 independent genomic loci of T-DNA integration sites in the AT1P plants. Mapping of the integration sites revealed that the chromosomal distribution of these sites is similar to that observed in conventional T-DNA knock-out lines, except that the intragenic type of integration is slightly lower (27%) in the AT1P plants compared to that observed in other random knock-out populations (30-35%). Ten AT2P lines that showed dominant phenotypes were chosen to monitor expression levels of genes adjacent to the T-DNA integration sites by RT-PCR. Activation was observed in 7 out of 17 of the adjacent genes detected. Genes located up to 8.2 kb away from the enhancer sequence were activated. One of the seven activated genes was located close to the left-border sequence of the T-DNA, having an estimated distance of 5.7 kb from the enhancer. Surprisingly, one gene, the first ATG of which is located 12 kb away from the enhancer, showed reduced mRNA accumulation in the tagged line. Application of the database generated to Arabidopsis functional genomics research is discussed. The sequence database of the 1172 loci from the AT1P plants is available (http://pfgweb.gsc.riken.go.jp/index.html).

MeSH Terms
Adenosine Triphosphate/metabolism Arabidopsis/genetics,growth & development,microbiology Base Sequence DNA Primers DNA, Bacterial/genetics DNA, Single-Stranded/genetics Databases, Nucleic Acid Genome, Plant Mutagenesis, Insertional Phenotype Polymerase Chain Reaction/methods Reverse Transcriptase Polymerase Chain Reaction
Chemicals
DNA Primers DNA, Bacterial DNA, Single-Stranded T-DNA Adenosine Triphosphate
Authors & Affiliations
14 authors, click to expand affiliations / ORCID
Ichikawa Takanari
Plant Function Exploration Team, Plant Functional Genomics Research Group, Genomic Sciences Center, RIKEN, 1-7-22 Suehiro-cho, Tsurumiku, Yokohama, Kanagawa 230-0045, Japan.
Nakazawa Miki
Kawashima Mika
Muto Shu
Gohda Kazushi
Suzuki Kumiko
Ishikawa Akie
Kobayashi Hiroko
Yoshizumi Takeshi
Tsumoto Yuko
Tsuhara Yumi
Iizumi Haruko
Goto Yukiko
Matsui Minami
Article Info
Journal
The Plant journal : for cell and molecular biology
Abbr.
Plant J
ISSN
0960-7412
Published
2003-11-00
Pages
421-9
Language
English
Region
England
NLM ID
9207397
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]