Gene Organization in Rice Revealed by Full-Length cDNA Mapping and Gene Expression Analysis through Microarray

Rice (Oryza sativa L.) is a model organism for the functional genomics of monocotyledonous plants since the genome size is considerably smaller than those of other monocotyledonous plants. Although highly accurate genome sequences of indica and japonica rice are available, additional resources such...

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Vydáno v:PloS one Ročník 2; číslo 11; s. e1235
Hlavní autoři: Satoh, Kouji, Doi, Koji, Nagata, Toshifumi, Kishimoto, Naoki, Suzuki, Kohji, Otomo, Yasuhiro, Kawai, Jun, Nakamura, Mari, Hirozane-Kishikawa, Tomoko, Kanagawa, Saeko, Arakawa, Takahiro, Takahashi-Iida, Juri, Murata, Mitsuyoshi, Ninomiya, Noriko, Sasaki, Daisuke, Fukuda, Shiro, Tagami, Michihira, Yamagata, Harumi, Kurita, Kanako, Kamiya, Kozue, Yamamoto, Mayu, Kikuta, Ari, Bito, Takahito, Fujitsuka, Nahoko, Ito, Kazue, Kanamori, Hiroyuki, Choi, Il-Ryong, Nagamura, Yoshiaki, Matsumoto, Takashi, Murakami, Kazuo, Matsubara, Ken-ichi, Carninci, Piero, Hayashizaki, Yoshihide, Kikuchi, Shoshi
Médium: Journal Article
Jazyk:angličtina
Vydáno: United States Public Library of Science 28.11.2007
Public Library of Science (PLoS)
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ISSN:1932-6203, 1932-6203
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Abstract Rice (Oryza sativa L.) is a model organism for the functional genomics of monocotyledonous plants since the genome size is considerably smaller than those of other monocotyledonous plants. Although highly accurate genome sequences of indica and japonica rice are available, additional resources such as full-length complementary DNA (FL-cDNA) sequences are also indispensable for comprehensive analyses of gene structure and function. We cross-referenced 28.5K individual loci in the rice genome defined by mapping of 578K FL-cDNA clones with the 56K loci predicted in the TIGR genome assembly. Based on the annotation status and the presence of corresponding cDNA clones, genes were classified into 23K annotated expressed (AE) genes, 33K annotated non-expressed (ANE) genes, and 5.5K non-annotated expressed (NAE) genes. We developed a 60mer oligo-array for analysis of gene expression from each locus. Analysis of gene structures and expression levels revealed that the general features of gene structure and expression of NAE and ANE genes were considerably different from those of AE genes. The results also suggested that the cloning efficiency of rice FL-cDNA is associated with the transcription activity of the corresponding genetic locus, although other factors may also have an effect. Comparison of the coverage of FL-cDNA among gene families suggested that FL-cDNA from genes encoding rice- or eukaryote-specific domains, and those involved in regulatory functions were difficult to produce in bacterial cells. Collectively, these results indicate that rice genes can be divided into distinct groups based on transcription activity and gene structure, and that the coverage bias of FL-cDNA clones exists due to the incompatibility of certain eukaryotic genes in bacteria.
AbstractList Rice (Oryza sativa L.) is a model organism for the functional genomics of monocotyledonous plants since the genome size is considerably smaller than those of other monocotyledonous plants. Although highly accurate genome sequences of indica and japonica rice are available, additional resources such as full-length complementary DNA (FL-cDNA) sequences are also indispensable for comprehensive analyses of gene structure and function. We cross-referenced 28.5K individual loci in the rice genome defined by mapping of 578K FL-cDNA clones with the 56K loci predicted in the TIGR genome assembly. Based on the annotation status and the presence of corresponding cDNA clones, genes were classified into 23K annotated expressed (AE) genes, 33K annotated non-expressed (ANE) genes, and 5.5K non-annotated expressed (NAE) genes. We developed a 60mer oligo-array for analysis of gene expression from each locus. Analysis of gene structures and expression levels revealed that the general features of gene structure and expression of NAE and ANE genes were considerably different from those of AE genes. The results also suggested that the cloning efficiency of rice FL-cDNA is associated with the transcription activity of the corresponding genetic locus, although other factors may also have an effect. Comparison of the coverage of FL-cDNA among gene families suggested that FL-cDNA from genes encoding rice- or eukaryote-specific domains, and those involved in regulatory functions were difficult to produce in bacterial cells. Collectively, these results indicate that rice genes can be divided into distinct groups based on transcription activity and gene structure, and that the coverage bias of FL-cDNA clones exists due to the incompatibility of certain eukaryotic genes in bacteria.
Rice (Oryza sativa L.) is a model organism for the functional genomics of monocotyledonous plants since the genome size is considerably smaller than those of other monocotyledonous plants. Although highly accurate genome sequences of indica and japonica rice are available, additional resources such as full-length complementary DNA (FL-cDNA) sequences are also indispensable for comprehensive analyses of gene structure and function. We cross-referenced 28.5K individual loci in the rice genome defined by mapping of 578K FL-cDNA clones with the 56K loci predicted in the TIGR genome assembly. Based on the annotation status and the presence of corresponding cDNA clones, genes were classified into 23K annotated expressed (AE) genes, 33K annotated non-expressed (ANE) genes, and 5.5K non-annotated expressed (NAE) genes. We developed a 60mer oligo-array for analysis of gene expression from each locus. Analysis of gene structures and expression levels revealed that the general features of gene structure and expression of NAE and ANE genes were considerably different from those of AE genes. The results also suggested that the cloning efficiency of rice FL-cDNA is associated with the transcription activity of the corresponding genetic locus, although other factors may also have an effect. Comparison of the coverage of FL-cDNA among gene families suggested that FL-cDNA from genes encoding rice- or eukaryote-specific domains, and those involved in regulatory functions were difficult to produce in bacterial cells. Collectively, these results indicate that rice genes can be divided into distinct groups based on transcription activity and gene structure, and that the coverage bias of FL-cDNA clones exists due to the incompatibility of certain eukaryotic genes in bacteria.Rice (Oryza sativa L.) is a model organism for the functional genomics of monocotyledonous plants since the genome size is considerably smaller than those of other monocotyledonous plants. Although highly accurate genome sequences of indica and japonica rice are available, additional resources such as full-length complementary DNA (FL-cDNA) sequences are also indispensable for comprehensive analyses of gene structure and function. We cross-referenced 28.5K individual loci in the rice genome defined by mapping of 578K FL-cDNA clones with the 56K loci predicted in the TIGR genome assembly. Based on the annotation status and the presence of corresponding cDNA clones, genes were classified into 23K annotated expressed (AE) genes, 33K annotated non-expressed (ANE) genes, and 5.5K non-annotated expressed (NAE) genes. We developed a 60mer oligo-array for analysis of gene expression from each locus. Analysis of gene structures and expression levels revealed that the general features of gene structure and expression of NAE and ANE genes were considerably different from those of AE genes. The results also suggested that the cloning efficiency of rice FL-cDNA is associated with the transcription activity of the corresponding genetic locus, although other factors may also have an effect. Comparison of the coverage of FL-cDNA among gene families suggested that FL-cDNA from genes encoding rice- or eukaryote-specific domains, and those involved in regulatory functions were difficult to produce in bacterial cells. Collectively, these results indicate that rice genes can be divided into distinct groups based on transcription activity and gene structure, and that the coverage bias of FL-cDNA clones exists due to the incompatibility of certain eukaryotic genes in bacteria.
Audience Academic
Author Kishimoto, Naoki
Suzuki, Kohji
Yamagata, Harumi
Matsumoto, Takashi
Yamamoto, Mayu
Murakami, Kazuo
Carninci, Piero
Otomo, Yasuhiro
Bito, Takahito
Satoh, Kouji
Hirozane-Kishikawa, Tomoko
Ito, Kazue
Choi, Il-Ryong
Nagamura, Yoshiaki
Kurita, Kanako
Murata, Mitsuyoshi
Arakawa, Takahiro
Kikuchi, Shoshi
Nagata, Toshifumi
Matsubara, Ken-ichi
Tagami, Michihira
Kawai, Jun
Kamiya, Kozue
Kanagawa, Saeko
Takahashi-Iida, Juri
Hayashizaki, Yoshihide
Fujitsuka, Nahoko
Kanamori, Hiroyuki
Doi, Koji
Fukuda, Shiro
Nakamura, Mari
Kikuta, Ari
Ninomiya, Noriko
Sasaki, Daisuke
AuthorAffiliation 4 Nara Institute of Science and Technology (NAIST), Ikoma, Nara, Japan
5 Genome Exploration Research Group, Genomic Sciences Center, RIKEN Yokohama Institute, Yokohama, Kanagawa, Japan
7 Institute of the Society for Techno-innovation of Agriculture, Forestry and Fisheries, Tsukuba, Ibaraki, Japan
2 Hitachi Software Engineering, Shinagawa-ku, Tokyo, Japan
8 Plant Breeding, Genetics and Biotechnology Division, International Rice Research Institute, DAPO, Metro Manila, Philippines
Umeå Plant Science Centre, Sweden
6 Genome Science Laboratory, RIKEN Wako Institute, Wako, Saitama, Japan
3 Laboratory of Genome Sequencing and Analysis Group, Foundation for Advancement of International Science (FAIS), Tsukuba, Ibaraki, Japan
1 Division of Genome and Biodiversity Research, National Institute of Agrobiological Sciences, Tsukuba, Ibaraki, Japan
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/18043742$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Copyright COPYRIGHT 2007 Public Library of Science
2007 Satoh et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Satoh et al. 2007
Copyright_xml – notice: COPYRIGHT 2007 Public Library of Science
– notice: 2007 Satoh et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
– notice: Satoh et al. 2007
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Conceived and designed the experiments: YH PC JK S Kikuchi K Matsubara K Murakami. Performed the experiments: K Kamiya K Kurita MY AK TB NF KI YN SF MT NN HK TM K Satoh YO IC MN TH S Kanagawa TA JT MM DS HY. Analyzed the data: K Satoh TN K Suzuki KD. Contributed reagents/materials/analysis tools: K Satoh NK. Wrote the paper: K Satoh IC.
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Snippet Rice (Oryza sativa L.) is a model organism for the functional genomics of monocotyledonous plants since the genome size is considerably smaller than those of...
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StartPage e1235
SubjectTerms Analysis
Artificial chromosomes
Bacteria
Bioassays
Biodiversity
Biological activity
Biological assays
Biotechnology
Chromosome Mapping
Classification
Cloning
Complementary DNA
Coverage
Deoxyribonucleic acid
DNA
DNA microarrays
DNA, Complementary - genetics
DNA, Plant - genetics
E coli
Exons
Gene expression
Gene Expression Profiling
Gene families
Gene loci
Gene mapping
Gene sequencing
Genes
Genetics and Genomics/Plant Genetics and Gene Expression
Genomes
Genomics
Incompatibility
Introns
Loci
Mapping
Nucleotide sequence
Oryza - genetics
Oryza sativa indica
Oryza sativa japonica
Plant Biology/Plant Genetics and Gene Expression
Plant genetics
Rice
Structure-function relationships
Transcription
Transcription (Genetics)
Transcription factors
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Title Gene Organization in Rice Revealed by Full-Length cDNA Mapping and Gene Expression Analysis through Microarray
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