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Featured researches published by Engkong Tan.


Scientific Reports | 2015

Dramatic improvement in genome assembly achieved using doubled-haploid genomes

Hong Zhang; Engkong Tan; Yutaka Suzuki; Yusuke Hirose; Shigeharu Kinoshita; Hideyuki Okano; Jun Kudoh; Atsushi Shimizu; Kazuyoshi Saito; Shugo Watabe; Shuichi Asakawa

Improvement in de novo assembly of large genomes is still to be desired. Here, we improved draft genome sequence quality by employing doubled-haploid individuals. We sequenced wildtype and doubled-haploid Takifugu rubripes genomes, under the same conditions, using the Illumina platform and assembled contigs with SOAPdenovo2. We observed 5.4-fold and 2.6-fold improvement in the sizes of the N50 contig and scaffold of doubled-haploid individuals, respectively, compared to the wildtype, indicating that the use of a doubled-haploid genome aids in accurate genome analysis.


Diseases of Aquatic Organisms | 2014

Characterization and antimicrobial susceptibility of motile aeromonads isolated from freshwater ornamental fish showing signs of septicaemia.

SSSdS Jagoda; Tg Wijewardana; Appudurai Arulkanthan; Yoji Igarashi; Engkong Tan; Shigeharu Kinoshita; Shugo Watabe; Shuichi Asakawa

A total of 74 phenotypically identified presumptive motile Aeromonas isolates recovered from septicaemic freshwater ornamental fish in Sri Lanka were genetically characterized by sequencing of rpoD and gyrB genes. rpoD/gyrB phylogeny confirmed only 53 isolates as Aeromonas, among which A. veronii was the predominant species (79.2%), followed by A. hydrophila (7.5%), A. caviae (5.7%), A. jandaei (1.9%), A. dhakensis (3.8%) and A. entero pelogenes (1.9%). The aeromonads confirmed by sequencing were further subjected to 16S rDNA PCR-RFLP which substantiated sequencing results for 83% of isolates. Fingerprinting of A. enteropelogenes (n = 42) using ERIC-PCR revealed no dominant clones, and the majority were genetically distinct. All isolates were screened by PCR for 7 virulence determinant genes (aer, act, ast, alt, fla, ser, exu) and 2 integrase encoding genes (intI1, intI2). Each isolate contained ≥3 of the virulence genes tested for, with a heterogeneous distribution. Of the isolates, 77% harboured the intI1 gene, while none had intI2. In vitro antimicrobial susceptibility testing showed highest resistances towards tetracycline (58.5%) and erythromycin (54.7%). Our results indicate the diverse range of aeromonads that could potentially be associated with motile aeromonad septicaemia in ornamental fish. This is the first isolation of A. dhakensis from a septicaemic ornamental fish since its original description from the same host.


Conservation Genetics Resources | 2014

Development of 16 microsatellite markers in Eusideroxylon zwageri by next-generation sequencing

Hiroyuki Kurokochi; Engkong Tan; Shuichi Asakawa; Sukartiningsih; Yoko Saito; Yuji Ide

The Ulin, Eusideroxylon zwageri, is a useful tropical tree now threatened by excessive logging. We used next-generation sequencing to isolate and characterize 16 polymorphic and codominant microsatellite (simple sequence repeat) markers in 32 E. zwageri trees in east Kalimantan, Indonesia. The number of alleles for each locus ranged from 2 to 19 and observed and expected heterozygosities ranged from 0.13 to 0.91 and from 0.18 to 0.92, respectively. These microsatellites may be useful for genetic studies and conservation of E. zwageri.


Gene | 2016

Different gene expression profiles between normal and thermally selected strains of rainbow trout, Oncorhynchus mykiss, as revealed by comprehensive transcriptome analysis.

Engkong Tan; Shigeharu Kinoshita; Yutaka Suzuki; Toshinao Ineno; Koichi Tamaki; Akio Kera; Koji Muto; Takashi Yada; Shoji Kitamura; Shuichi Asakawa; Shugo Watabe

A high-temperature selected (HT) strain of rainbow trout was established from the Donaldson (DS) strain by traditional selective breeding in Japan. The aim of this study is to investigate genes related to upper temperature tolerance in this strain utilizing next generation sequencer (NGS), and to establish comprehensive and comparable datasets in brain, liver, muscle, heart and gill tissues between the HT and DS strains. After assembling, clustering and filtering, 242,530 contigs were obtained. Among them, 7624 transcripts had at least 10 counts in expression analysis in all tissues and used as references. BLASTX homology search showed that 7329 transcripts matched with known genes. Compared to the DS strain, the HT strain expressed 90, 775, 349, 188 and 194 genes 2 folds or more in brain, liver, muscle, heart, and gill, respectively in the case of fish before heat-exposure treatment. Meanwhile, the HT strain expressed 292, 363, 433, 322 and 211 genes 2 folds or more in brain, liver, muscle, heart, and gill, respectively in case of fish after heat-exposure treatment. Many of heat shock protein family genes and transcription factor AP-1 related genes were highly expressed in all tissues of the HT strain compared with the DS strain. These results suggest that these genes play key roles in upper temperature tolerance. These comprehensive and comparable datasets will offer broad visions for upper temperature tolerance in fish species.


International Journal of Molecular Sciences | 2014

Transcriptional responses of a bicarbonate-tolerant monocot, Puccinellia tenuiflora, and a related bicarbonate-sensitive species, Poa annua, to NaHCO3 stress.

Shio Kobayashi; Hina Satone; Engkong Tan; Hiroyuki Kurokochi; Shuichi Asakawa; Shenkui Liu; Tetsuo Takano

Puccinellia tenuiflora is an alkaline salt-tolerant monocot found in saline-alkali soil in China. To identify the genes which are determining the higher tolerance of P. tenuiflora compared to bicarbonate sensitive species, we examined the responses of P. tenuiflora and a related bicarbonate-sensitive Poeae plant, Poa annua, to two days of 20 mM NaHCO3 stress by RNA-seq analysis. We obtained 28 and 38 million reads for P. tenuiflora and P. annua, respectively. For each species, the reads of both unstressed and stressed samples were combined for de novo assembly of contigs. We obtained 77,329 contigs for P. tenuiflora and 115,335 contigs for P. annua. NaHCO3 stress resulted in greater than two-fold absolute expression value changes in 157 of the P. tenuiflora contigs and 1090 of P. annua contigs. Homologs of the genes involved in Fe acquisition, which are important for the survival of plants under alkaline stress, were up-regulated in P. tenuiflora and down-regulated in P. annua. The smaller number of the genes differentially regulated in P. tenuiflora suggests that the genes regulating bicarbonate tolerance are constitutively expressed in P. tenuiflora.


Genome Announcements | 2014

Draft Genome Sequence of Aeromonas hydrophila Strain Ae34, Isolated from a Septicemic and Moribund Koi Carp (Cyprinus carpio koi), a Freshwater Aquarium Fish.

S. S. S. D. S. Jagoda; Engkong Tan; Appudurai Arulkanthan; Shigeharu Kinoshita; Shugo Watabe; Shuichi Asakawa

ABSTRACT Aeromonas hydrophila is an important opportunistic pathogen that infects a variety of aquatic and terrestrial animals, including humans. We report here the draft genome sequence of A. hydrophila Ae34, a multidrug-resistant isolate from the kidney of a moribund koi carp (Ciprinus carpio koi) with signs of hemorrhagic septicemia.


Journal of Forest Research | 2015

Development of 18 microsatellite markers in Pieris japonica, a poisonous tree insulated from the browsing pressure of herbivores, using a next-generation sequencer

Hiroyuki Kurokochi; Engkong Tan; Shuichi Asakawa; Chunlan Lian

Pieris japonica is a poisonous tree species that is rarely eaten by herbivorous animals, which could allow it to expand its distribution and change ecosystems. Using a next-generation sequencer, 18 microsatellite markers were isolated from P. japonica and characterized. The number of alleles at each locus ranged from 2 to 11. The observed and expected heterozygosities ranged from 0.13 to 1.00 and 0.32 to 0.88, respectively. These markers will be useful for genetic studies of P. japonica, which will be essential for conservation of its surrounding environment.


Conservation Genetics Resources | 2014

Fifteen novel microsatellite markers for two Amphiprion species (Amphiprion frenatus and Amphiprion perideraion) and cross-species amplification

Masaaki Sato; Hiroyuki Kurokochi; Engkong Tan; Shuichi Asakawa; Kentaro Honda; Klenthon O. Bolisay; Yohei Nakamura; Chunlan Lian; Miguel D. Fortes; Masahiro Nakaoka

Abstract Anemonefishes are popular model species for research on population connectivity via larval dispersal, and understanding this connectivity is beneficial when designing marine protected areas. We developed 15 microsatellite markers for two anemonefishes, Amphiprion frenatus and Amphiprion perideraion. Of these 15 markers, 10 worked well for both species, while three were specific for A. frenatus and two were specific for A. perideraion. For A. frenatus, the number of alleles at each locus ranged from 4 to 28, and the observed and expected heterozygosities ranged from 0.258 to 0.938 and from 0.285 to 0.953, respectively. For A. perideraion, the respective numbers were 4–14, 0.344–0.969, and 0.412–0.868. These microsatellite markers will be useful for the study of population connectivity in these two species.


Comparative Biochemistry and Physiology Part D: Genomics and Proteomics | 2017

Global gene expression analysis of the muscle tissues of medaka acclimated to low and high environmental temperatures

Daisuke Ikeda; Hiroki Koyama; Nanami Mizusawa; Nobuhiro Kanno; Engkong Tan; Shuichi Asakawa; Shugo Watabe

Medaka (Oryzias latipes) is a temperate eurythermal fish that is able to survive over a wide range of water temperatures ranging from near zero to over 30°C throughout the year; it maintains its normal physiological and biochemical processes through temperature acclimation. To determine the mechanisms involved in temperature acclimation of fish, the fast skeletal muscle tissues of medaka underwent global gene expression analysis using next-generation sequencing. Ten individuals were placed into two aquariums at 24°C. While the water temperature of one aquarium was decreased to 10°C, that of the other aquarium was increased to 30°C; these temperatures were subsequently maintained for 5weeks. RNA sequencing (RNA-Seq) analyses revealed that 11 genes involved in energy metabolism and muscle atrophy were significantly highly expressed in the 10°C-acclimated fish. Meanwhile, significantly higher expression levels were observed for 20 genes encoding myofibrillar proteins and heat shock proteins in the 30°C-acclimated fish. Moreover, 1103 genes had at least fourfold differential expression between the acclimation groups. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses provided important information: although the expression of genes related to metabolic processes were activated, muscle atrophy occurred in the 10°C-acclimated fish, and muscle cells divided actively in the 30°C-acclimated fish and avoided thermal stress by expressing heat shock proteins. Therefore, RNA-Seq analyses with the available genome database will be useful for better understanding the molecular mechanisms involved in the temperature acclimation of fish.


Immunogenetics | 2015

Characterization of the torafugu (Takifugu rubripes) immunoglobulin heavy chain gene locus

Xi Fu; Hong Zhang; Engkong Tan; Shugo Watabe; Shuichi Asakawa

In this study, we investigated the immunoglobulin heavy (IGH) gene locus of torafugu (Takifugu rubripes) from publicly available assembly sequences and presented an annotated locus map, including the IGHV genes, pseudogenes, and IGHC genes. Three new IGHV gene families (IGHV3–IGHV5) were discovered. We observed the interspersion of IGHV1 and IGHV2 family members and that they often intermingled with each other, while other family members were further interspersed. Conservation of the promoter and recombination signal sequences (RSS) was observed in a family-specific manner. In addition to known variable region genes present on chromosome 5 (current torafugu genome assembly), we found 34 additional IGHV genes on scaffold 287 and three novel potentially functional IGHD genes on scaffold 483. In total, the variable region of the torafugu IGH locus consists of at least 48 IGHV genes, seven IGHD genes, and six IGHJ genes. IGHC genes have also been mapped in this study, with three genes encoding immunoglobulin classes: IgT, IgM, and IgD. We confirmed the expression of newly identified IGHV3 family sequences in the spleen and kidney of adult torafugu and found a favorable IGHV segment usage by IgM and IgT. Possible structural variation in the IGHδ locus was observed based on the current torafugu assembly. The complete characterization of the torafugu IGH locus will facilitate detailed studies of large-scale mechanisms associated with the recombination of the variable region genes and will offer insights into the genetic basis of the potential diversity in the antibody response observed in torafugu.

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