Yue-Qin Chen
Ministry of Education
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Publication
Featured researches published by Yue-Qin Chen.
Proceedings of the National Academy of Sciences of the United States of America | 2007
Xiaofei Zhang; Yue-Qin Chen; Congying Wang; Li Yen Mae Huang
It has been generally assumed that the cell body (soma) of a neuron, which contains the nucleus, is mainly responsible for synthesis of macromolecules and has a limited role in cell-to-cell communication. Using sniffer patch recordings, we show here that electrical stimulation of dorsal root ganglion (DRG) neurons elicits robust vesicular ATP release from their somata. The rate of release events increases with the frequency of nerve stimulation; external Ca2+ entry is required for the release. FM1–43 photoconversion analysis further reveals that small clear vesicles participate in exocytosis. In addition, the released ATP activates P2X7 receptors in satellite cells that enwrap each DRG neuron and triggers the communication between neuronal somata and glial cells. Blocking L-type Ca2+ channels completely eliminates the neuron–glia communication. We further show that activation of P2X7 receptors can lead to the release of tumor necrosis factor-α (TNFα) from satellite cells. TNFα in turn potentiates the P2X3 receptor-mediated responses and increases the excitability of DRG neurons. This study provides strong evidence that somata of DRG neurons actively release transmitters and play a crucial role in bidirectional communication between neurons and surrounding satellite glial cells. These results also suggest that, contrary to the conventional view, neuronal somata have a significant role in cell–cell signaling.
Systematic Biology | 2005
Peng Zhang; Hui Zhou; Yue-Qin Chen; Yi-Fei Liu; Liang-Hu Qu
Establishing the relationships among modern amphibians (lissamphibians) and their ancient relatives is necessary for our understanding of early tetrapod evolution. However, the phylogeny is still intractable because of the highly specialized anatomy and poor fossil record of lissamphibians. Paleobiologists are still not sure whether lissamphibians are monophyletic or polyphyletic, and which ancient group (temnospondyls or lepospondyls) is most closely related to them. In an attempt to address these problems, eight mitochondrial genomes of living amphibians were determined and compared with previously published amphibian sequences. A comprehensive molecular phylogenetic analysis of nucleotide sequences yields a highly resolved tree congruent with the traditional hypotheses (Batrachia). By using a molecular clock-independent approach for inferring dating information from molecular phylogenies, we present here the first molecular timescale for lissamphibian evolution, which suggests that lissamphibians first emerged about 330 million years ago. By observing the fit between molecular and fossil times, we suggest that the temnospondyl-origin hypothesis for lissamphibians is more credible than other hypotheses. Moreover, under this timescale, the potential geographic origins of the main living amphibian groups are discussed: (i) advanced frogs (neobatrachians) may possess an Africa-India origin; (ii) salamanders may have originated in east Asia; (iii) the tropic forest of the Triassic Pangaea may be the place of origin for the ancient caecilians. An accurate phylogeny with divergence times can be also helpful to direct the search for missing fossils, and can benefit comparative studies of amphibian evolution.
FEBS Letters | 2006
Yu-Chun Luo; Hui Zhou; Yan Li; Jun-Yu Chen; Jian-Hua Yang; Yue-Qin Chen; Liang-Hu Qu
In vitro cultured embryogenic callus was employed as a model to investigate microRNAs (miRNAs) associated with embryogenesis and post‐embryonic development. Thirty‐one miRNAs including 16 novel species were identified from a large number of small RNAs which were cloned from both differentiated and undifferentiated rice embryogenic calli. Four target genes of the miRNAs were further validated. A set of the miRNAs, including miR397 and miR156, exhibited intriguing expression patterns during the transition from undifferentiated to differentiated calli. By exploiting the correlations between the differential expression patterns of these miRNAs and their targets, the regulatory roles of the miRNAs on meristem maintenance and embryogenesis were indicated.
FEMS Microbiology Ecology | 2003
Li-Nan Huang; Yue-Qin Chen; Hui Zhou; Shuo Luo; Chong-Yu Lan; Liang-Hu Qu
Cultivation-independent molecular approaches were used to investigate the phylogenetic composition of Archaea and the relative abundance of phylogenetically defined groups of methanogens in the leachate of a closed municipal solid waste landfill. Cloning and phylogenetic analysis of archaeal 16S rRNA gene sequences (16S rDNA) revealed that the landfill leachate harbored a diverse Archaea community, with sequence types distributed within the two archaeal kingdoms of the Euryarchaeota and the Crenarchaeota. Of the 80 clones examined, 51 were phylogenetically associated with well-defined methanogen lineages covering two major methanogenic phenotypes; 20 were related to Thermoplasma and were grouped with some novel archaeal rRNA gene sequences recently recovered from various anaerobic habitats; finally, five belonged to Crenarchaeota and were not closely related to any hitherto cultivated species. Most of the methanogen-like clones were affiliated with the hydrogenotrophic Methanomicrobiales and the methylotrophic and acetoclastic Methanosarcinales. Quantitative oligonucleotide hybridization experiments showed that methanogens in the leachate accounted for only a very small fraction of the total community (approximately 2%) and that Methanomicrobiales and Methanosarcinales constituted the majority of the total methanogenic population.
Nucleic Acids Research | 2008
Yan Li; Jun Luo; Hui Zhou; Jian-You Liao; Li-Ming Ma; Yue-Qin Chen; Liang-Hu Qu
Giardia lamblia is an early diverging and evolutionarily successful protozoan as it can enter into a dormant cyst stage from a vegetative trophozoite. During dormant stage, its metabolic rate decreases dramatically. However, to date, the regulatory molecules participating in the initiation and maintenance of this process have not been fully investigated. In this study, we have identified a class of abundant small RNAs named sitRNAs, which are ∼46 nucleotides in length and accumulate in G. lamblia encysting cultures. Remarkably, they are derived from the 3′ portion of fully matured tRNAs by cleavage of the anticodon left arm, with the 3′ terminal CCA triplex still connected. During differentiation, only a limited portion of mature tRNAs is cleaved, but this cleavage occurs almost in the entire tRNA family. sitRNAs begin to accumulate as early as 3 h after initiation of encystation and are maintained at a relatively stable level during the whole process, exhibiting an expression peak at around 24 hr. Our studies further show that sitRNAs can be induced by several other stress factors, and in the case of serum deprivation, both tRNAs and sitRNAs degrade rapidly, with the accumulation of tRNA being halved. Our results may provide new insight into a novel mechanism for stressed G. lamblia to regulate gene expression globally.
Gene | 2003
Peng Zhang; Yue-Qin Chen; Yi-Fei Liu; Hui Zhou; Liang-Hu Qu
The mitochondrial genome of the Chinese giant salamander Andrias davidianus was isolated using the long-and-accurate polymerase chain reaction (LA PCR) method. The sequencing work adopted the shotgun strategy accompanying with seven internal primers to cover the gaps where overlapping clones were not available. The entire mtDNA sequence is 16,503 bp long, with a gene content of 13 protein-coding, two ribosomal RNA and 22 transfer RNA genes, and order identical to that observed in most other vertebrates except for an additional 318 bp non-coding sequence between tRNA-Thr and tRNA-Pro genes. In order to carry out molecular phylogenetic analyses, all 13 protein sequences deduced from whole mitochondrial genomes for eight vertebrate species (six amphibians, two lobe-finned fishes) were combined to a single data set. This data set was refined by the program Gblocks using a stringent parameter setting and then subjected to MP, ML and NJ analyses. Thus phylogenetic relationships among living amphibians were discussed.
Molecular Phylogenetics and Evolution | 2003
Peng Zhang; Yue-Qin Chen; Hui Zhou; Xiu-Ling Wang; Liang-Hu Qu
The Amphibia were the dominant land Vertebrates in the Carboniferous and were certainly the stock from which the reptiles and in turn the mammals and birds evolved. Although two major groups of extinct amphibians, the Labyrinthodontia and the Lepospondyli did not last beyond the Triassic, amphibian lines evidently continued and are represented today by the three distinctly different groups of modern Amphibia (Lissamphibia), the Caudata, Anura, and Gymnophiona. The monophyly of the Lissamphibia and their phylogenetic relationships are still debated. The most widely accepted hypothesis, based on morphological data, supports the monophyletic origin in the Late Paleozoic (300myr) of the three living amphibian orders and a sister-group relationship between Anura and Caudata (the Batrachia hypothesis) (Laurin and Reisz, 1997; Trueb and Cloutier, 1991). However, Jarvik (1980) has suggested that Lissamphibia is not a natural group and hypothesized a polyphyletic origin of the three living orders. Carroll and coworkers (Carroll, 1988; Carroll and Holmes, 1980) have advocated a close phylogenetic relationship between salamanders and caecilians. According to these authors, frogs would have evolved from temnospondyl amphibians (Apsidospondyli) whereas salamanders and caecilians originated from different lineages of microsaurs (Lepospondyli). The affinity between salamanders and caecilians is also supported by several morphological (Bolt, 1991) and molecular (Feller and Hedges, 1998; Hedges et al., 1990) phylogenetic
Plant Biotechnology Journal | 2014
Congying Wang; Shengchun Zhang; Yang Yu; Yu-Chun Luo; Qing Liu; Changliang Ju; Yu-Chan Zhang; Liang-Hu Qu; William J. Lucas; Xiaojing Wang; Yue-Qin Chen
Plant laccase (LAC) enzymes belong to the blue copper oxidase family and polymerize monolignols into lignin. Recent studies have established the involvement of microRNAs in this process; however, physiological functions and regulation of plant laccases remain poorly understood. Here, we show that a laccase gene, LAC4, regulated by a microRNA, miR397b, controls both lignin biosynthesis and seed yield in Arabidopsis. In transgenic plants, overexpression of miR397b (OXmiR397b) reduced lignin deposition. The secondary wall thickness of vessels and the fibres was reduced in the OXmiR397b line, and both syringyl and guaiacyl subunits are decreased, leading to weakening of vascular tissues. In contrast, overexpression of miR397b-resistant laccase mRNA results in an opposite phenotype. Plants overexpressing miR397b develop more than two inflorescence shoots and have an increased silique number and silique length, resulting in higher seed numbers. In addition, enlarged seeds and more seeds are formed in these miR397b overexpression plants. The study suggests that miR397-mediated development via regulating laccase genes might be a common mechanism in flowering plants and that the modulation of laccase by miR397 may be potential for engineering plant biomass production with less lignin.
Nucleic Acids Research | 2004
Jia‐Fu Wang; Hui Zhou; Yue-Qin Chen; Qing‐Jun Luo; Liang-Hu Qu
Proceedings of the National Academy of Sciences of the United States of America | 2006
Peng Zhang; Yue-Qin Chen; Hui Zhou; Yi-Fei Liu; Xiu-Ling Wang; Theodore J. Papenfuss; David B. Wake; Liang-Hu Qu