Ann-Shyn Chiang

Prof. Ann-Shyn Chiang


Research Focus & Metrics

Academic Career Length

37Years (1990-Present)

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

Representative Publications

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1 January 2011 in Current Biology
Verified
Journal Article
Closed access
ACAnn-Shyn Chiang
Ann-Shyn Chiang
CLChih-Yung Lin
Chih-Yung Lin
CCChao-Chun Chuang
Chao-Chun Chuang
HCHsiu-Ming Chang
Hsiu-Ming Chang
CHChang-Huain Hsieh
Chang-Huain Hsieh
JHJenn-Kang Hwang
Jenn-Kang Hwang

18 November 2019 in Nature Nanotechnology
Verified
Journal Article
Closed access
PDF file
YSYun-Chieh Sung
Yun-Chieh Sung
PJPei-Ru Jin
Pei-Ru Jin
LCLi-An Chu
Li-An Chu
FHFu-Fei Hsu
Fu-Fei Hsu
MWMei-Ren Wang
Mei-Ren Wang
YCYunching Chen
Yunching Chen

1 May 2015 in Current Biology
Verified
Journal Article
Closed access
CSChi-Tin Shih
Chi-Tin Shih
OSOlaf Sporns
Olaf Sporns
SYShou-Li Yuan
Shou-Li Yuan
TSTa-Shun Su
Ta-Shun Su
YLYen-Jen Lin
Yen-Jen Lin
ACAnn-Shyn Chiang
Ann-Shyn Chiang

10 February 2012 in Science
Verified
Journal Article
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CCChun-Chao Chen
Chun-Chao Chen
JWJie-Kai Wu
Jie-Kai Wu
HLHsuan-Wen Lin
Hsuan-Wen Lin
TPTsung-Pin Pai
Tsung-Pin Pai
TFTsai-Feng Fu
Tsai-Feng Fu
ACAnn-Shyn Chiang
Ann-Shyn Chiang
Challenging the Mushroom Bodies: Early memory is labile and is gradually consolidated over time into long-lasting, stable memory. In several species, including mammals, memory consolidation depends on protein synthesis. In Drosophila , long-term memory is produced by spaced repetitive training, which induces cyclic adenosine monophosphate (cAMP)–response element–binding protein (CREB)–dependent gene transcription and de novo protein synthesis. Using a large number of genetic tools, Chen et al. (p. 678 ; see the Perspective by Dubnau ) localized this CREB-dependent induction of de novo protein synthesis to two dorsal-anterior-lateral neurons in the adult brain. Importantly, protein synthesis was not required within the mushroom bodies, which are usually considered to be the site of associative learning and memory in insects.

1 April 2005 in Current Biology
Verified
Journal Article
Closed access
SXShouzhen Xia
Shouzhen Xia
TMTomoyuki Miyashita
Tomoyuki Miyashita
TFTsai-Feng Fu
Tsai-Feng Fu
WLWei-Yong Lin
Wei-Yong Lin
CWChia-Lin Wu
Chia-Lin Wu
ACAnn-Shyn Chiang
Ann-Shyn Chiang

16 August 2011 in Proceedings of the National Academy of Sciences
Verified
Journal Article
Open access
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PLPei-Tseng Lee
Pei-Tseng Lee
HLHsuan-Wen Lin
Hsuan-Wen Lin
YCYu-Hsuan Chang
Yu-Hsuan Chang
TFTsai-Feng Fu
Tsai-Feng Fu
JDJosh Dubnau
Josh Dubnau
ACAnn-Shyn Chiang
Ann-Shyn Chiang
Pavlovian olfactory learning in Drosophila produces two genetically distinct forms of intermediate-term memories: anesthesia-sensitive memory, which requires the amnesiac gene, and anesthesia-resistant memory (ARM), which requires the radish gene. Here, we report that ARM is specifically enhanced or inhibited in flies with elevated or reduced serotonin (5HT) levels, respectively. The requirement for 5HT was additive with the memory defect of the amnesiac mutation but was occluded by the radish mutation. This result suggests that 5HT and Radish protein act on the same pathway for ARM formation. Three supporting lines of evidence indicate that ARM formation requires 5HT released from only two dorsal paired medial (DPM) neurons onto the mushroom bodies (MBs), the olfactory learning and memory center in Drosophila : ( i ) DPM neurons were 5HT-antibody immunopositive; ( ii ) temporal inhibition of 5HT synthesis or release from DPM neurons, but not from other serotonergic neurons, impaired ARM formation; ( iii ) knocking down the expression of d5HT1A serotonin receptors in α/β MB neurons, which are innervated by DPM neurons, inhibited ARM formation. Thus, in addition to the Amnesiac peptide required for anesthesia-sensitive memory formation, the two DPM neurons also release 5HT acting on MB neurons for ARM formation.