Woongghi Shin

Woongghi Shin


Research Focus & Metrics

Academic Career Length

27Years (2000-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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18 July 2012 in Proceedings of the National Academy of Sciences
Verified
Journal Article
Open access
HJHae Jin Jeong
Hae Jin Jeong
YYYeong Du Yoo
Yeong Du Yoo
NKNam Seon Kang
Nam Seon Kang
ALAn Suk Lim
An Suk Lim
KSKyeong Ah Seong
Kyeong Ah Seong
KLKitack Lee
Kitack Lee
Survival of free-living and symbiotic dinoflagellates ( Symbiodinium spp.) in coral reefs is critical to the maintenance of a healthy coral community. Most coral reefs exist in oligotrophic waters, and their survival strategy in such nutrient-depleted waters remains largely unknown. In this study, we found that two strains of Symbiodinium spp. cultured from the environment and acquired from the tissues of the coral Alveopora japonica had the ability to feed heterotrophically. Symbiodinium spp. fed on heterotrophic bacteria, cyanobacteria ( Synechococcus spp.), and small microalgae in both nutrient-replete and nutrient-depleted conditions. Cultured free-living Symbiodinium spp. displayed no autotrophic growth under nitrogen-depleted conditions, but grew when provided with prey. Our results indicate that Symbiodinium spp.’s mixotrophic activity greatly increases their chance of survival and their population growth under nitrogen-depleted conditions, which tend to prevail in coral habitats. In particular, free-living Symbiodinium cells acquired considerable nitrogen from algal prey, comparable to or greater than the direct uptake of ammonium, nitrate, nitrite, or urea. In addition, free-living Symbiodinium spp. can be a sink for planktonic cyanobacteria ( Synechococcus spp.) and remove substantial portions of Synechococcus populations from coral reef waters. Our discovery of Symbiodinium ’s feeding alters our conventional views of the survival strategies of photosynthetic Symbiodinium and corals.

2 September 2009 in Journal of Eukaryotic Microbiology
Verified
Journal Article
Closed access
PDF file
YYYeong Du Yoo
Yeong Du Yoo
HJHae Jin Jeong
Hae Jin Jeong
MKMi Seon Kim
Mi Seon Kim
NKNam Seon Kang
Nam Seon Kang
JSJae Yoon Song
Jae Yoon Song
KLKitack Lee
Kitack Lee

9 September 2010 in Molecular Ecology
Verified
Journal Article
Closed access
PDF file
SBSung Min Boo
Sung Min Boo
HKHan Soon Kim
Han Soon Kim
WSWoongghi Shin
Woongghi Shin
GBGa Hun Boo
Ga Hun Boo
SCSung Mi Cho
Sung Mi Cho
HYHwan Su Yoon
Hwan Su Yoon

1 June 2015 in American Journal of Botany
Verified
Journal Article
Closed access
PDF file
PSPeter A. Siver
Peter A. Siver
BJBok Yeon Jo
Bok Yeon Jo
JKJong Im Kim
Jong Im Kim
WSWoongghi Shin
Woongghi Shin
ALAnne Marie Lott
Anne Marie Lott
AWAlexander P. Wolfe
Alexander P. Wolfe

4 July 2017 in Genome Biology and Evolution
Verified
Journal Article
Open access
PDF file
JKJong Im Kim
Jong Im Kim
CMChrista E. Moore
Christa E. Moore
JAJohn M. Archibald
John M. Archibald
DBDebashish Bhattacharya
Debashish Bhattacharya
GYGangman Yi
Gangman Yi
WSWoongghi Shin
Woongghi Shin
Cryptophytes are an ecologically important group of largely photosynthetic unicellular eukaryotes. This lineage is of great interest to evolutionary biologists because their plastids are of red algal secondary endosymbiotic origin and the host cell retains four different genomes (host nuclear, mitochondrial, plastid, and red algal nucleomorph). Here, we report a comparative analysis of plastid genomes from six representative cryptophyte genera. Four newly sequenced cryptophyte plastid genomes of Chroomonas mesostigmatica, Ch. placoidea, Cryptomonas curvata, and Storeatula sp. CCMP1868 share a number of features including synteny and gene content with the previously sequenced genomes of Cryptomonas paramecium, Rhodomonas salina, Teleaulax amphioxeia, and Guillardia theta. Our analysis of these plastid genomes reveals examples of gene loss and intron insertion. In particular, the chlB/chlL/chlN genes, which encode light-independent (dark active) protochlorophyllide oxidoreductase (LIPOR) proteins have undergone recent gene loss and pseudogenization in cryptophytes. Comparison of phylogenetic trees based on plastid and nuclear genome data sets show the introduction, via secondary endosymbiosis, of a red algal derived plastid in a lineage of chlorophyll-c containing algae. This event was followed by additional rounds of eukaryotic endosymbioses that spread the red lineage plastid to diverse groups such as haptophytes and stramenopiles.

24 March 2012 in Journal of Phycology
Verified
Journal Article
Closed access
PDF file
MKMiran Kim
Miran Kim
SNSeung Won Nam
Seung Won Nam
WSWoongghi Shin
Woongghi Shin
DCD. Wayne Coats
D. Wayne Coats
MPMyung Gil Park
Myung Gil Park