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Analysis of germinating seed stage expressed sequence tags in Oryza sativa L

Authors :
Jang-Ho Hahn
Gun-Wook Kim
Doh-Won Yun
Jung-Sook Lee
Hyeonso Ji
Gang-Seob Lee
Ung-Han Yoon
Chang-Kug Kim
Sung-Han Park
Tae-Ho Lee
Yong Hwan Kim
Mi-Suk Seo
Jeonghwa Lee
Source :
Journal of Plant Biotechnology. 36:281-288
Publication Year :
2009
Publisher :
The Korean Society for Plant Biotechnology, 2009.

Abstract

Seed germination is the important stage to ex-press many genes for regulation of energy metabolism, starch degradation and cell division from seed dormancy state. For the functional analysis of seed germination mech-anisms, we were analyzed the rice cDNA clones ( Oryza sativa cultivar Ilpum ) obtained from seed imbibition during 48 hours. Total number of 18,101 Expressed Sequence Tags (ESTs) were clustered using SeqMan program. Among them, 8,836 clones were identified as unique clones. We identified the chitinase gene specifically expressed in seed germination and amylase gene involved to starch degradation from the full length cDNA analysis, and several genes were registered to NCBI GeneBank. To analyzed the commonly expressed genes between inmature seed and germinated seed, 25,668 inmature ESTs and 18,101 germinated ESTs were clustered using SeqMan program and identified 2,514 clones as com-monly expressed unigene. Among them, alpha-glubulin and alcohol dehydrogenase I were supposed to LEA genes only expressed in the immature and germinated seed stages.For the clustering of orthologous group genes, we further analyzed the 8,836 EST clones from germinating seeds using NCBI clusters of orthologous groups database. Among the clones, 5,076 clones were categorized into information storage and processing, cellular processes and signaling, metabolism and poorly characterized genes, proportioning 783 (14.29%), 1,484 (27%), 1,363 (24.8%) and 1,869 (34%) clones to the previous four categories, respectively.

Details

ISSN :
12292818
Volume :
36
Database :
OpenAIRE
Journal :
Journal of Plant Biotechnology
Accession number :
edsair.doi...........6b5bf24bc20b89b60e71ebad29b928f5