Functional Annotation of a Full-Length Arabidopsis cDNA Collection

Author:

Seki Motoaki12,Narusaka Mari1,Kamiya Asako1,Ishida Junko1,Satou Masakazu1,Sakurai Tetsuya1,Nakajima Maiko1,Enju Akiko1,Akiyama Kenji1,Oono Youko23,Muramatsu Masami45,Hayashizaki Yoshihide45,Kawai Jun45,Carninci Piero45,Itoh Masayoshi45,Ishii Yoshiyuki45,Arakawa Takahiro45,Shibata Kazuhiro45,Shinagawa Akira45,Shinozaki Kazuo12

Affiliation:

1. Plant Mutation Exploration Team, Plant Functional Genomics Research Group, RIKEN Genomic Sciences Center (GSC), 3-1-1 Koyadai, Tsukuba 305-0074, Japan.

2. Laboratory of Plant Molecular Biology, RIKEN Tsukuba Institute, 3-1-1 Koyadai, Tsukuba 305-0074, Japan.

3. Master's Program in Biosystem Studies, University of Tsukuba, Tennoudai, Tsukuba, Ibaraki, 305-0074, Japan.

4. Laboratory for Genome Exploration Research Group, RIKEN GSC, Yokohama Institute 1-7-22 Suehiro-cho, Tsurumi-ku, Yokokama, Kanagawa, 230-0045, Japan.

5. Genome Science Laboratory, RIKEN, 2-1 Hirosawa, Wako, 351-0198, Japan.

Abstract

Full-length complementary DNAs (cDNAs) are essential for the correct annotation of genomic sequences and for the functional analysis of genes and their products. We isolated 155,144 RIKEN Arabidopsis full-length (RAFL) cDNA clones. The 3′-end expressed sequence tags (ESTs) of 155,144 RAFL cDNAs were clustered into 14,668 nonredundant cDNA groups, about 60% of predicted genes. We also obtained 5′ ESTs from 14,034 nonredundant cDNA groups and constructed a promoter database. The sequence database of the RAFL cDNAs is useful for promoter analysis and correct annotation of predicted transcription units and gene products. Furthermore, the full-length cDNAs are useful resources for analyses of the expression profiles, functions, and structures of plant proteins.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference31 articles.

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