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Silicon transporter genes of Fragilariopsis cylindrus (Bacillariophyceae) are differentially expressed during the progression of cell cycle synchronized by Si or lightopen access

Authors
Oh, Han SangLee, Sung-eunHan, Chae-seongKim, JoonNam, OnyouSeo, SeungbeomChang, Kwang SukJin, EonSeonHwang, Yong-sic
Issue Date
Jun-2018
Publisher
KOREAN SOC PHYCOLOGY
Keywords
biomineralization; cell wall; psychrophilic diatom; silicon transporter gene; synchrony
Citation
ALGAE, v.33, no.2, pp.191 - 203
Indexed
SCIE
SCOPUS
KCI
Journal Title
ALGAE
Volume
33
Number
2
Start Page
191
End Page
203
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/16895
DOI
10.4490/algae.2018.33.5.8
ISSN
1226-2617
Abstract
Fragilariopsis cylindrus is one of the most successful psychrophiles in the Southern Ocean. To investigate the molecular mechanism of biomineralization in this species, we attempted to synchronize F. cylindrus growth, since new cell wall formation is tightly coupled to the cell division process. Nutrient limitation analysis showed that F. cylindrus cultures rapidly stopped growing when deprived of silicate or light, while growth continued to a certain extent in the absence of nitrate. Flow cytometry analysis indicated that deprivation of either silicate or light could effectively arrest the cell cycle of this diatom species at the GI phase, suggesting that synchrony can be established using either factor. Fluorescence labeling of new cell walls was faintly detectable as early as approximately 6 h after silicon repletion or light irradiation, and labeling was markedly intensified by 18 h. It is revealed that the synthesis of girdle bands begins before valve synthesis in this species, with active valve synthesis occurring during the G2 / M phase. Expression profiling revealed that selective member(s) of the F. cylindrus SIT genes (FcSIT) respond to silicate and light, with a different set of genes being responsive to each factor. The Si / light double depletion experiments demonstrated that expression of one FcS/Tgene is possibly correlated to transition to G2 / M phase of the cell cycle, when the valve is actively formed.
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