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Annotation and expression profile analysis of cIDNAs from the Antarctic diatom Chaetoceros neogracile

Authors
Jung, GyeongseoLee, Choul-GyunKang, Sung-HoJin, Eonseon
Issue Date
Aug-2007
Publisher
한국미생물·생명공학회
Keywords
Chaetoceros neogracile; antarctic diatom; ESTs; cold adaptation
Citation
Journal of Microbiology and Biotechnology, v.17, no.8, pp 1330 - 1337
Pages
8
Indexed
SCIE
SCOPUS
KCI
Journal Title
Journal of Microbiology and Biotechnology
Volume
17
Number
8
Start Page
1330
End Page
1337
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/179771
ISSN
1017-7825
1738-8872
Abstract
To better understand the gene expression of the cold-adapted polar diatom, we conducted a survey of the Chaetoceros neogracile transcriptome by cDNA sequencing and expression of interested cDNAs from the Antarctic diatom. A non-normalized cDNA library was constructed from the C. neogracile, and a total of 2,500 cDNAs were sequenced to generate 1,881 high-quality expressed sequence tags (ESTs) (accession numbers EL620615-EL622495). Based on their clustering, we identified 154 unique clusters comprising 342 ESTs. The remaining 1,540 ESTs did not cluster. The number of unique genes identified in the data set is thus estimated to be 1,694. Taking advantage of various tools and databases, putative functions were assigned to 939 (55.4%) of these genes. Of the remaining 540 (31.9%) unknown sequences, 215 (12.7%) appeared to be C. neogracile-specific since they lacked any significant sequence similarity to any sequence available in the public databases. C. neogracile consisted of a relatively high percentage of genes involved in metabolism, genetic information processing, cellular processes, defense or stress resistance, photosynthesis, structure, and signal transduction. From the ESTs, the expression of these putative C. neogracile genes was investigated: fucoxanthin chlorophyll (chl) a,c-binding protein (FCP), ascorbate peroxidase (ASP), and heat-shock protein 90 (HSP90). The abundance of ASP and HSP90 changed substantially in response to different culture conditions, indicating the possible regulation of these genes in C. neogracile.
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