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Dive into the research topics where Chiou-Rong Sheue is active.

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Featured researches published by Chiou-Rong Sheue.


Taxon | 2003

Kandelia obovata (Rhizophoraceae), a new mangrove species from Eastern Asia

Chiou-Rong Sheue; Ho-Yih Liu; Jean W. H. Yong

Kandelia (Rhizophoraceae) has long been regarded as a monotypic mangrove genus. Recent studies in chromosome number, molecular phylogeography, physiological adaptation, and leaf anatomy, however, reveal that there are twowell differentiated sets of geographical populations separated by the South China Sea. These are recognized as two distinct species, Kandelia candel (L.) Druce and Kandelia obovata Sheue, Liu & Yong sp. nov.


Proceedings of the National Academy of Sciences of the United States of America | 2013

Anatomical and transcriptional dynamics of maize embryonic leaves during seed germination

Wen Yu Liu; Yao Ming Chang; Sean Chun Chang Chen; Chen Hua Lu; Yeh Hwa Wu; Mei Yeh Jade Lu; Di Rong Chen; Arthur Chun-Chieh Shih; Chiou-Rong Sheue; H.-C. Huang; Chun Ping Yu; Hsin-Hung Lin; Shin Han Shiu; Maurice Sun Ben Ku; Wen-Hsiung Li

Our anatomical analysis revealed that a dry maize seed contains four to five embryonic leaves at different developmental stages. Rudimentary kranz structure (KS) is apparent in the first leaf with a substantial density, but its density decreases toward younger leaves. Upon imbibition, leaf expansion occurs rapidly with new KSs initiated from the palisade-like ground meristem cells in the middle of the leaf. In parallel to the anatomical analysis, we obtained the time course transcriptomes for the embryonic leaves in dry and imbibed seeds every 6 h up to hour 72. Over this time course, the embryonic leaves exhibit transcripts of 30,255 genes at a level that can be regarded as “expressed.” In dry seeds, ∼25,500 genes are expressed, showing functional enrichment in transcription, RNA processing, protein synthesis, primary metabolic pathways, and calcium transport. During the 72-h time course, ∼13,900 genes, including 590 transcription factor genes, are differentially expressed. Indeed, by 30 h postimbibition, ∼2,200 genes expressed in dry seeds are already down-regulated, and ∼2,000 are up-regulated. Moreover, the top 1% expressed genes at 54 h or later are very different from those before 30 h, reflecting important developmental and physiological transitions. Interestingly, clusters of genes involved in hormone metabolism, signaling, and responses are differentially expressed at various time points and TF gene expression is also modular and stage specific. Our dataset provides an opportunity for hypothesizing the timing of regulatory actions, particularly in the context of KS development.


Annals of Botany | 2012

Natural foliar variegation without costs? The case of Begonia

Chiou-Rong Sheue; Shang Horng Pao; Lee-Feng Chien; Peter Chesson; Ching-I Peng

BACKGROUND AND AIMS Foliar variegation is recognized as arising from two major mechanisms: leaf structure and pigment-related variegation. Begonia has species with a variety of natural foliar variegation patterns, providing diverse examples of this phenomenon. The aims of this work are to elucidate the mechanisms underlying different foliar variegation patterns in Begonia and to determine their physiological consequences. METHODS Six species and one cultivar of Begonia were investigated. Light and electron microscopy revealed the leaf structure and ultrastructure of chloroplasts in green and light areas of variegated leaves. Maximum quantum yields of photosystem II were measured by chlorophyll fluorescence. Comparison with a cultivar of Ficus revealed key features distinguishing variegation mechanisms. KEY RESULTS Intercellular space above the chlorenchyma is the mechanism of variegation in these Begonia. This intercellular space can be located (a) below the adaxial epidermis or (b) below the adaxial water storage tissue (the first report for any taxa), creating light areas on a leaf. In addition, chlorenchyma cell shape and chloroplast distribution within chlorenchyma cells differ between light and green areas. Chloroplasts from both areas showed dense stacking of grana and stroma thylakoid membranes. The maximum quantum yield did not differ significantly between these areas, suggesting minimal loss of function with variegation. However, the absence of chloroplasts in light areas of leaves in the Ficus cultivar led to an extremely low quantum yield. CONCLUSIONS Variegation in these Begonia is structural, where light areas are created by internal reflection between air spaces and cells in a leaf. Two forms of air space structural variegation occur, distinguished by the location of the air spaces. Both forms may have a common origin in development where dermal tissue becomes loosely connected to mesophyll. Photosynthetic functioning is retained in light areas, and these areas do not include primary veins, potentially limiting the costs of variegation.


American Journal of Botany | 2007

Bizonoplast, a unique chloroplast in the epidermal cells of microphylls in the shade plant Selaginella erythropus (Selaginellaceae).

Chiou-Rong Sheue; Vassilios Sarafis; Ruth Kiew; Ho-Yih Liu; Alexandre Salino; Ling-Long Kuo-Huang; Yuen-Po Yang; Chi-Chu Tsai; Chun-Hung Lin; Jean W. H. Yong; Maurice S. B. Ku

Study of the unique leaf anatomy and chloroplast structure in shade-adapted plants will aid our understanding of how plants use light efficiently in low light environments. Unusual chloroplasts in terms of size and thylakoid membrane stacking have been described previously in several deep-shade plants. In this study, a single giant cup-shaped chloroplast, termed a bizonoplast, was found in the abaxial epidermal cells of the dorsal microphylls and the adaxial epidermal cells of the ventral microphylls in the deep-shade spike moss Selaginella erythropus. Bizonoplasts are dimorphic in ultrastructure: the upper zone is occupied by numerous layers of 2-4 stacked thylakoid membranes while the lower zone contains both unstacked stromal thylakoids and thylakoid lamellae stacked in normal grana structure oriented in different directions. In contrast, other cell types in the microphylls contain chloroplasts with typical structure. This unique chloroplast has not been reported from any other species. The enlargement of epidermal cells into funnel-shaped, photosynthetic cells coupled with specific localization of a large bizonoplast in the lower part of the cells and differential modification in ultrastructure within the chloroplast may allow the plant to better adapt to low light. Further experiments are required to determine whether this shade-adapted organism derives any evolutionary or ecophysiological fitness from these unique chloroplasts.


Journal of Ethnopharmacology | 2008

The molecular mechanism of gypenosides-induced G1 growth arrest of rat hepatic stellate cells

Ming-Ho Chen; Shu-Hsin Chen; Qwa-Fun Wang; Jung-Chou Chen; De-Ching Chang; Shih-Lan Hsu; Ching-Hsein Chen; Chiou-Rong Sheue; Yi-Wen Liu

AIM OF THE STUDY Gypenosides, the saponins extract derived from Gynostemma pentaphyllum Makino, have been used for treating hepatitis and cancer in Asia. Our previous study demonstrates that gypenosides inhibit the onset and improve the recovery of liver fibrosis induced by CCl4 in rats. In this study, we used the isolated rat hepatic stellate cells (HSCs) as a model to study the cellular mechanism of gypenosides-inhibited liver fibrosis. MATERIALS AND METHODS Rat HSCs was treated with PDGF, gypenosides or vehicle. Cell viability was assessed by trypan blue staining. Apoptosis and cell cycle were evaluated by flow cytometry. The activation or inhibition of signal molecules was detected by Western blotting. RESULTS Our results showed that 500 microg/ml gypenosides decreased PDGF-induced rat HSCs numbers (8750+/-2629 versus 103,000+/-6683, p<0.001, 95% confidence interval) and arrested cells at the G1 phase without the presence of sub-G1 fraction. Analysis of PDGF-induced proliferative molecules including phosphorylation of Akt and p70 S6K, gypenosides inhibited the activation of this signal pathway. Furthermore, gypenosides down-regulated the protein expression of cell cycle G1-specific cyclin D1 and D3. CONCLUSIONS Gypenosides inhibited PDGF-induced HSCs proliferation by inhibiting the signal pathway of PDGF-Akt-p70 S6K and down-regulation of cyclin D1 and D3 expression.


Blumea | 2009

On the morphology and molecular basis of segregation of Ceriops zippeliana and C. decandra (Rhizophoraceae) from Asia.

Chiou-Rong Sheue; H.-Y. Liu; C.-C. Tsai; S.M.A. Rashid; J.W.H. Yong; Yuen-Po Yang

Ceriops zippeliana, a member of the mangrove Rhizophoraceae, was first reported in 1849. It was considered to be a synonym of C. decandra, which is still widely accepted. We present morphological and molecular evidence to show that C. zippeliana is significantly distinct from C. decandra, and illustrations and an identification key to both species.


Journal of Experimental Botany | 2016

Phytoplasma SAP11 alters 3-isobutyl-2-methoxypyrazine biosynthesis in Nicotiana benthamiana by suppressing NbOMT1

Choon Meng Tan; Chia-Hua Li; Nai-Wen Tsao; Li-Wen Su; Yen-Ting Lu; Shu Heng Chang; Yi Yu Lin; Jyun-Cyuan Liou; Li-Ching Hsieh; Jih-Zu Yu; Chiou-Rong Sheue; Sheng-Yang Wang; Chin-Fa Lee; Jun-Yi Yang

Highlight Phytoplasma effector SAP11 modulates plant volatile organic compound emissions by suppressing the expression of NbOMT1, which encodes an O-methyltransferase required for the biosynthesis of 3-isobutyl-2-methoxypyrazine.


American Journal of Botany | 2015

A variation on chloroplast development: The bizonoplast and photosynthetic efficiency in the deep-shade plant Selaginella erythropus

Chiou-Rong Sheue; Jian Wei Liu; Jia Fang Ho; Ai Wen Yao; Yeh Hua Wu; Sauren Das; Chi Chu Tsai; Hsiu An Chu; Maurice S. B. Ku; Peter Chesson

UNLABELLED • PREMISE OF THE STUDY Chloroplast development and structure are highly conserved in vascular plants, but the bizonoplast of Selaginella is a notable exception. In the shade plant S. erythropus, each dorsal epidermal cell contains one bizonoplast, while other cells have normal chloroplasts. Our quest was to (1) determine the origin of bizonoplasts, (2) explore developmental plasticity, and (3) correlate developmental changes with photosynthetic activity to provide insights unavailable in other green plants with more constrained development.• METHODS Bizonoplast development was studied in juvenile prostrate and older erect shoots of S. erythropus. Plastid plasticity was studied in plants cultivated under different light conditions. Chlorophyll fluorescence was measured and correlated with photosynthetic activity.• KEY RESULTS The bizonoplast originates from a proplastid, forming a distinctive upper zone rapidly after exposure to low light. In the prostrate shoots, the proplastid develops through early stages only. When the shoot becomes erect, the proplastid soon develops into a mature bizonoplast. Erect shoots have significantly higher photosynthetic efficiency than prostrate shoots. No bizonoplasts were found in the plants growing in high light, where 2-4 spheroidal chloroplasts formed, or with light from below.• CONCLUSIONS The upper zone develops above a normal-looking chloroplast structure to produce a bizonoplast. Bizonoplast developmental plasticity suggests that regular lamellar structure and monoplastidy are adaptations to deep shade environments. Such novel variation in S. erythropus is in stark contrast to known plastid development in other vascular plants, possibly reflecting retention of developmental flexibility in the basal clade, Lycophyta, to which it belongs.


Journal of Microscopy | 2012

Second harmonic generation imaging of the deep shade plant Selaginella erythropus using multifunctional two‐photon laser scanning microscopy

A.H. Reshak; Chiou-Rong Sheue

Background: Multifunctional two‐photon laser scanning microscopy provides attractive advantages over conventional two‐photon laser scanning microscopy. For the first time, simultaneous measurement of the second harmonic generation (SHG) signals in the forward and backward directions and two photon excitation fluorescence were achieved from the deep shade plant Selaginella erythropus.


Journal of Plant Biology | 2010

Phylogenetics and Biogeography of the Phalaenopsis violacea (Orchidaceae) Species Complex Based on Nuclear and Plastid DNA

Chi-Chu Tsai; Chiou-Rong Sheue; Chih-Hsiung Chen; Chang-Hung Chou

The Phalaenopsis violacea complex includes two species: P. violacea Witte and Phalaenopsis bellina (Rchb.f.) E. A. Christ. However, three forms of P. violacea have been found in different areas, including Sumatra, the Malay Peninsula, and Mentawai Island. The phylogenetic tree inferred from the internal transcribed spacer (ITS) region of nuclear ribosomal DNA (nrDNA), the trnL intron, and the atpB-rbcL spacer of plastid DNA were used to clarify the phylogenetics and biogeography of the P. violacea complex. Analyses of the trnL intron sequences and of the atpB-rbcL spacer did not allow for apparent discrimination among these three species of the P. violacea complex. Based on the phylogenetic tree inferred from the ITS sequence, P. bellina cannot be separated from populations of P. violacea, with the exception of the population distributed on Mentawai Is., Indonesia. Based on morphological characteristics, P. violacea distributed on Mentawai Is. has a long and roundish rachis and is separate from the other groups of the P. violacea complex described by Christenson (Timber, Portland, OR, 2001). Therefore, the results of this study show a trend that supports the conclusion that the population of the P. violacea complex on Mentawai Is. is a separate species from P. violacea. Based on the biogeography of the P. violacea complex, Mentawai plants of this complex might be descended from those on the Sumatra/Malay Peninsula.

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Yuen-Po Yang

National Sun Yat-sen University

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Chi-Chu Tsai

National Pingtung University of Science and Technology

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Chi Chu Tsai

National Pingtung University of Science and Technology

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Ho-Yih Liu

National Sun Yat-sen University

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Jian Wei Liu

National Chung Hsing University

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Yuen Po Yang

National Sun Yat-sen University

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Sauren Das

Indian Statistical Institute

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Chang-Fu Hsieh

National Taiwan University

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