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Dive into the research topics where Ryuji J. Machida is active.

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Featured researches published by Ryuji J. Machida.


Marine Biotechnology | 2002

Complete mitochondrial DNA sequence of Tigriopus japonicus (Crustacea: Copepoda).

Ryuji J. Machida; Masaki Miya; Mutsumi Nishida; Shuhei Nishida

The complete nucleotide sequence of the mitochondrial genome was determined for a harpacticoid copepod, Tigriopus japonicus (Crustacea), using an approach that employs a long polymerase chain reaction technique and primer walking. Although the genome (14,628 bp) contained the same set of 37 genes (2 ribosomal RNA, 22 transfer RNA, and 13 protein-coding genes) as found in other metazoan animals, none of the previously reported gene orders were comparable to that of T. japonicus. Furthermore, all genes were encoded on one strand, unlike the mitochondrial genomes of most metazoan animals. Size reductions were notable for tRNA and rRNA genes, resulting in one of the smallest mitochondrial genomes in the arthropod lineage. Although it appears that such large-scale gene rearrangements have occurred in the ancestral species of T. japonicus, none of the proposed mechanisms parsimoniously account for this eccentric gene arrangement.


BMC Genomics | 2009

Zooplankton diversity analysis through single-gene sequencing of a community sample

Ryuji J. Machida; Yasuyuki Hashiguchi; Mutsumi Nishida; Shuhei Nishida

BackgroundOceans cover more than 70% of the earths surface and are critical for the homeostasis of the environment. Among the components of the ocean ecosystem, zooplankton play vital roles in energy and matter transfer through the system. Despite their importance, understanding of zooplankton biodiversity is limited because of their fragile nature, small body size, and the large number of species from various taxonomic phyla. Here we present the results of single-gene zooplankton community analysis using a method that determines a large number of mitochondrial COI gene sequences from a bulk zooplankton sample. This approach will enable us to estimate the species richness of almost the entire zooplankton community.ResultsA sample was collected from a depth of 721 m to the surface in the western equatorial Pacific off Pohnpei Island, Micronesia, with a plankton net equipped with a 2-m2 mouth opening. A total of 1,336 mitochondrial COI gene sequences were determined from the cDNA library made from the sample. From the determined sequences, the occurrence of 189 species of zooplankton was estimated. BLASTN search results showed high degrees of similarity (>98%) between the query and database for 10 species, including holozooplankton and merozooplankton.ConclusionIn conjunction with the Census of Marine Zooplankton and Barcode of Life projects, single-gene zooplankton community analysis will be a powerful tool for estimating the species richness of zooplankton communities.


Marine Biotechnology | 2004

PCR-based approach for sequencing mitochondrial genomes of decapod crustaceans, with a practical example from kuruma prawn (Marsupenaeus japonicus).

Mitsugu M. Yamauchi; Masaki Miya; Ryuji J. Machida; Mutsumi Nishida

An approach for sequencing the entire mitochondrial genomes (mitogenomes) of decapod crustaceans using 79 newly designed and 7 published polymerase chain reaction (PCR) primers is described. The approach comprises the following steps: (1) the entire mitogenome is amplified in 2 or 3 long PCRs; (2) the 86 primers are used in different combinations to amplify contiguous, overlapping short segments of the entire mitogenome with the diluted long PCR products as templates; (3) direct cycle sequencing is conducted using the short PCR products. This strategy allows a more rapid determination of decapod mitogenomic sequences than a traditional method using cloned mitochondrial DNA and primer walking strategy. As a practical example, the mitogenomic sequence for a kuruma prawn Marsupenaeus japonicus (Crustacea: Decapoda), was determined using the PCR-based approach.


PLOS ONE | 2010

Dissimilarity of species and forms of planktonic Neocalanus copepods using mitochondrial COI, 12S, nuclear ITS, and 28S gene sequences.

Ryuji J. Machida; Atsushi Tsuda

Background A total of six Neocalanus species inhabit the oceans of the world. Of these, three species plus form variants (N. cristatus, N. plumchrus, N. flemingeri large form, and N. flemingeri small form), which constitute a monophyletic group among Neocalanus copepods, occur in the Northwestern Pacific off Japan. In the present study, we have tried to discriminate the three species plus form variants of Neocalanus copepods based on sequences of four DNA marker regions. Methodology/Principal Findings Discrimination was performed based on the DNA sequence information from four genetic markers, including the mitochondrial COI, 12S, nuclear ITS, and 28S gene regions. Sequence dissimilarity was compared using both distance- and character-based approaches. As a result, all three species were confirmed to be distinct based on the four genetic marker regions. On the contrary, distinction of the form variants was only confirmed based on DNA sequence of the mitochondrial COI gene region. Conclusions/Significance Although discrimination was not successful for the form variants based on the mitochondrial 12S, nuclear ITS, and 28S genes, diagnostic nucleotide sequence characters were observed in their mitochondrial COI gene sequences. Therefore, these form variants are considered to be an important unit of evolution below the species level, and constitute a part of the Neocalanus biodiversity.


Marine Biotechnology | 2004

Organization of the Mitochondrial Genome of Antarctic Krill Euphausia superba (Crustacea: Malacostraca)

Ryuji J. Machida; Masaki Miya; Mitsugu M. Yamauchi; Mutsumi Nishida; Shuhei Nishida

We determined the nearly complete DNA sequence of the mitochondrial genome of Antarctic krill Euphausia superba (Crustacea: Malacostraca), one of the most ecologically and commercially important zooplankters in Antarctic waters. All of the genome sequences were purified by gene amplification using long polymerase chain reaction (PCR), and the products were subsequently used as templates for either direct sequencing using a primer-walking strategy or nested PCR with crustacea-versatile primers. Although we were unable to determine a portion of the genome owing to technical difficulties, the sequenced position, 14,606 bp long, contained all of the 13 protein-coding genes, 19 of the 22 transfer RNA genes, and the large subunit as well as a portion of the small subunit ribosomal RNA genes. Gene rearrangement was observed for 3 transfer RNA genes (tRNACys, tRNATyr, and tRNATrp) and the 2 leucine tRNA genes.


Comparative Biochemistry and Physiology Part D: Genomics and Proteomics | 2010

Complete mitochondrial genome sequences of the three pelagic chaetognaths Sagitta nagae, Sagitta decipiens and Sagitta enflata

Hiroomi Miyamoto; Ryuji J. Machida; Shuhei Nishida

The complete nucleotide sequences of the mitochondrial genomes were determined for the three pelagic chaetognaths, Sagitta nagae, Sagitta decipiens, and Sagitta enflata. The mitochondrial genomes of these species which were 11,459, 11,121, and 12,631bp in length, respectively, contained 14 genes (11 protein-coding genes, one transfer RNA gene, and two ribosomal RNA genes), and were found to have lost 23 genes that are present in the typical metazoan mitochondrial genome. The same mitochondrial genome contents have been reported from the benthic chaetognaths belonging to the family Spadellidae, Paraspadella gotoi and Spadella cephaloptera. Within the phylum Chaetognatha, Sagitta and Spadellidae are distantly related, suggesting that the gene loss occurred in the ancestral species of the phylum. The gene orders of the three Sagitta species are markedly different from those of the other non-Chaetognatha metazoans. In contrast to the region with frequent gene rearrangements, no gene rearrangements were observed in the gene cluster encoding COII-III, ND1-3, srRNA, and tRNA(met). Within this conserved gene cluster, gene rearrangements were not observed in the three Sagitta species or between the Sagitta and Spadellidae species. The gene order of this cluster was also assumed to be the ancestral state of the phylum.


Journal of Natural History | 2005

Systematics and zoogeography of the deep‐sea hyperbenthic family Arietellidae (Copepoda: Calanoida) collected from the Sulu Sea

Susumu Ohtsuka; Shuhei Nishida; Ryuji J. Machida

A faunistic survey of the deep‐sea hyperbenthic copepods in the Sulu Sea, which has a deep basin and is connected via shallow straits with the Pacific and the South China Sea, was carried out in November and December 2002, using beam trawls and a mid‐water trawl. Two new genera and four new species of the primitive calanoid family Arietellidae are described. A new genus Metacalanalis shows intermediate characteristics between those of Metacalanus Cleve, 1901 and Pilarella Alvarez, 1985. Another new genus, Protoparamisophria, is closely related to Paramisophria Scott, 1897, but exhibits more plesiomorphic states in the female genital system and appendages. Two new species of the genera Paraugaptiloides Ohtsuka, Boxshall and Roe, 1994 and Sarsarietellus Campaner, 1984 are the second and the third species, respectively, for these genera. This discovery enhances the validity of these rare genera, and sheds light on the geological history of the Sulu Sea and the evolution of the Arietellidae within it.


PLOS ONE | 2017

Occurrence of mitochondrial CO1 pseudogenes in Neocalanus plumchrus (Crustacea: Copepoda): Hybridization indicated by recombined nuclear mitochondrial pseudogenes

Ryuji J. Machida; Ya-Ying Lin

A portion of the mitochondrial cytochrome c oxidase I gene was sequenced using both genomic DNA and complement DNA from three planktonic copepod Neocalanus species (N. cristatus, N. plumchrus, and N. flemingeri). Small but critical sequence differences in CO1 were observed between gDNA and cDNA from N. plumchrus. Furthermore, careful observation revealed the presence of recombination between sequences in gDNA from N. plumchrus. Moreover, a chimera of the N. cristatus and N. plumchrus sequences was obtained from N. plumchrus gDNA. The observed phenomena can be best explained by the preferential amplification of the nuclear mitochondrial pseudogenes from gDNA of N. plumchrus. Two conclusions can be drawn from the observations. First, nuclear mitochondrial pseudogenes are pervasive in N. plumchrus. Second, a mating between a female N. cristatus and a male N. plumchrus produced viable offspring, which further backcrossed to a N. plumchrus individual. These observations not only demonstrate intriguing mating behavior in these species, but also emphasize the importance of careful interpretation of species marker sequences amplified from gDNA.


Journal of Oceanography | 2007

Evidence for the grazing hypothesis: Grazing reduces phytoplankton responses of the HNLC ecosystem to iron enrichment in the western subarctic pacific (SEEDS II)

Atsushi Tsuda; Shigenobu Takeda; Hiroaki Saito; Jun Nishioka; Isao Kudo; Yukihiro Nojiri; Koji Suzuki; Mitsuo Uematsu; Mark L. Wells; Daisuke Tsumune; Takeshi Yoshimura; Tatsuo Aono; Takafumi Aramaki; William P. Cochlan; Maki Hayakawa; Keiri Imai; Tomoshi Isada; Yoko Iwamoto; William Keith Johnson; Sohiko Kameyama; Shungo Kato; Hiroshi Kiyosawa; Y. Kondo; Maurice Levasseur; Ryuji J. Machida; Ippei Nagao; Fumiko Nakagawa; Takahiro Nakanishi; Seiji Nakatsuka; Akira Narita


Gene | 2004

Large-scale gene rearrangements in the mitochondrial genomes of two calanoid copepods Eucalanus bungii and Neocalanus cristatus (Crustacea), with notes on new versatile primers for the srRNA and COI genes

Ryuji J. Machida; Masaki Miya; Mutsumi Nishida; Shuhei Nishida

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Masaki Miya

American Museum of Natural History

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Daisuke Tsumune

Central Research Institute of Electric Power Industry

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Dhugal J. Lindsay

Japan Agency for Marine-Earth Science and Technology

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