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\n \n\n \n \n Alavi, S. M. H., Matsumura, N., Shiba, K., Itoh, N., Takahashi, K. G, Inaba, K., & Osada, M.\n\n\n \n \n \n \n \n Roles of extracellular ions and pH in 5-HT-induced sperm motility in marine bivalve.\n \n \n \n \n\n\n \n\n\n\n REPRODUCTION, 147(3): 331–345. March 2014.\n \n\n\n\n
\n\n\n\n \n \n \"RolesPaper\n  \n \n\n \n \n doi\n  \n \n\n \n link\n  \n \n\n bibtex\n \n\n \n  \n \n abstract \n \n\n \n\n \n \n \n \n \n \n \n\n  \n \n \n\n\n\n
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@article{alavi_roles_2014,\n\ttitle = {Roles of extracellular ions and {pH} in 5-{HT}-induced sperm motility in marine bivalve},\n\tvolume = {147},\n\tissn = {1470-1626, 1741-7899},\n\turl = {https://rep.bioscientifica.com/view/journals/rep/147/3/331.xml},\n\tdoi = {10.1530/REP-13-0418},\n\tabstract = {Factors that inhibit and stimulate the initiation of sperm motility were determined for Manila clam (\n              Ruditapes\n              philippinarum\n              ), Pacific oyster (\n              Crassostrea gigas\n              ), and Japanese scallop (\n              Patinopecten yessoensis\n              ). Compared with artificial seawater (ASW), serotonin (5-hydroxytryptamine creatinine sulfate, 5-HT) could fully trigger sperm motility and increase sperm velocity and motility duration. Sperm motility was decreased in ASW at pH 6.5–7.0 and suppressed at pH 4.0. In Manila clam and Pacific oyster, 5-HT could overcome the inhibitory effects of acidic pH on sperm motility. In the presence of nigericin (a K\n              +\n              /H\n              +\n              exchanger), sperm motility was only triggered at pH 8.3. Testicular fluid K\n              +\n              concentrations were two- to fourfold higher than that in ASW. Sperm motility and velocity were decreased in ASW or 5-HT containing ≥40 mM K\n              +\n              or ≥2.5 mM 4-aminopyridine, suggesting K\n              +\n              efflux requirement to initiate motility. Sperm motility and velocity were reduced in ASW or 5-HT containing EGTA or W-7, suggesting that extracellular Ca\n              2\n              +\n              is required for Ca\n              2\n              +\n              /calmodulin-dependent flagellar beating. Ca\n              2\n              +\n              influx occurs via Ca\n              2\n              +\n              channels because sperm motility and velocity were decreased in both ASW and 5-HT containing T-type and L-type Ca\n              2\n              +\n              channel blockers. 5-HT-dependent initiation of sperm motility was associated with intracellular Ca\n              2\n              +\n              rise, which was comparable to that seen in ASW but was not observed in the presence of EGTA or a Ca\n              2\n              +\n              channel blocker. Extracellular Na\n              +\n              is also essential for sperm motility initiation via regulation of Na\n              +\n              /Ca\n              2\n              +\n              exchange. Overall, 5-HT-dependent initiation of sperm motility in marine bivalve mollusks is an osmolality-independent mechanism and regulated by extracellular pH, K\n              +\n              , Ca\n              2\n              +\n              , and Na\n              +\n              .},\n\tnumber = {3},\n\turldate = {2021-07-27},\n\tjournal = {REPRODUCTION},\n\tauthor = {Alavi, Sayyed Mohammad Hadi and Matsumura, Natsuki and Shiba, Kogiku and Itoh, Naoki and Takahashi, Keisuke G and Inaba, Kazuo and Osada, Makoto},\n\tmonth = mar,\n\tyear = {2014},\n\tpages = {331--345},\n}\n\n
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\n Factors that inhibit and stimulate the initiation of sperm motility were determined for Manila clam ( Ruditapes philippinarum ), Pacific oyster ( Crassostrea gigas ), and Japanese scallop ( Patinopecten yessoensis ). Compared with artificial seawater (ASW), serotonin (5-hydroxytryptamine creatinine sulfate, 5-HT) could fully trigger sperm motility and increase sperm velocity and motility duration. Sperm motility was decreased in ASW at pH 6.5–7.0 and suppressed at pH 4.0. In Manila clam and Pacific oyster, 5-HT could overcome the inhibitory effects of acidic pH on sperm motility. In the presence of nigericin (a K + /H + exchanger), sperm motility was only triggered at pH 8.3. Testicular fluid K + concentrations were two- to fourfold higher than that in ASW. Sperm motility and velocity were decreased in ASW or 5-HT containing ≥40 mM K + or ≥2.5 mM 4-aminopyridine, suggesting K + efflux requirement to initiate motility. Sperm motility and velocity were reduced in ASW or 5-HT containing EGTA or W-7, suggesting that extracellular Ca 2 + is required for Ca 2 + /calmodulin-dependent flagellar beating. Ca 2 + influx occurs via Ca 2 + channels because sperm motility and velocity were decreased in both ASW and 5-HT containing T-type and L-type Ca 2 + channel blockers. 5-HT-dependent initiation of sperm motility was associated with intracellular Ca 2 + rise, which was comparable to that seen in ASW but was not observed in the presence of EGTA or a Ca 2 + channel blocker. Extracellular Na + is also essential for sperm motility initiation via regulation of Na + /Ca 2 + exchange. Overall, 5-HT-dependent initiation of sperm motility in marine bivalve mollusks is an osmolality-independent mechanism and regulated by extracellular pH, K + , Ca 2 + , and Na + .\n
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\n \n\n \n \n Alavi, S. M. H., Postlerová-Maňásková, P., Hatef, A., Pšenička, M., Pěknicová, J., Inaba, K., Ciereszko, A., & Linhart, O.\n\n\n \n \n \n \n \n Protease in sturgeon sperm and the effects of protease inhibitors on sperm motility and velocity.\n \n \n \n \n\n\n \n\n\n\n Fish Physiology and Biochemistry, 40(5): 1393–1398. October 2014.\n \n\n\n\n
\n\n\n\n \n \n \"ProteasePaper\n  \n \n\n \n \n doi\n  \n \n\n \n link\n  \n \n\n bibtex\n \n\n \n\n \n\n \n \n \n \n \n \n \n\n  \n \n \n\n\n\n
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@article{alavi_protease_2014,\n\ttitle = {Protease in sturgeon sperm and the effects of protease inhibitors on sperm motility and velocity},\n\tvolume = {40},\n\tissn = {0920-1742, 1573-5168},\n\turl = {http://link.springer.com/10.1007/s10695-014-9933-8},\n\tdoi = {10.1007/s10695-014-9933-8},\n\tlanguage = {en},\n\tnumber = {5},\n\turldate = {2021-07-27},\n\tjournal = {Fish Physiology and Biochemistry},\n\tauthor = {Alavi, Sayyed Mohammad Hadi and Postlerová-Maňásková, Pavla and Hatef, Azadeh and Pšenička, Martin and Pěknicová, Jana and Inaba, Kazuo and Ciereszko, Andrzej and Linhart, Otomar},\n\tmonth = oct,\n\tyear = {2014},\n\tpages = {1393--1398},\n}\n\n
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\n \n\n \n \n Higuchi, T., Fujimura, H., Yuyama, I., Harii, S., Agostini, S., & Oomori, T.\n\n\n \n \n \n \n \n Biotic Control of Skeletal Growth by Scleractinian Corals in Aragonite–Calcite Seas.\n \n \n \n \n\n\n \n\n\n\n PLoS ONE, 9(3): e91021. March 2014.\n \n\n\n\n
\n\n\n\n \n \n \"BioticPaper\n  \n \n\n \n \n doi\n  \n \n\n \n link\n  \n \n\n bibtex\n \n\n \n\n \n  \n \n 7 downloads\n \n \n\n \n \n \n \n \n \n \n\n  \n \n \n\n\n\n
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@article{higuchi_biotic_2014,\n\ttitle = {Biotic {Control} of {Skeletal} {Growth} by {Scleractinian} {Corals} in {Aragonite}–{Calcite} {Seas}},\n\tvolume = {9},\n\tissn = {1932-6203},\n\turl = {https://dx.plos.org/10.1371/journal.pone.0091021},\n\tdoi = {10.1371/journal.pone.0091021},\n\tlanguage = {en},\n\tnumber = {3},\n\turldate = {2021-07-27},\n\tjournal = {PLoS ONE},\n\tauthor = {Higuchi, Tomihiko and Fujimura, Hiroyuki and Yuyama, Ikuko and Harii, Saki and Agostini, Sylvain and Oomori, Tamotsu},\n\teditor = {Roberts, John Murray},\n\tmonth = mar,\n\tyear = {2014},\n\tpages = {e91021},\n}\n\n
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\n \n\n \n \n Hiyama, G., Matsuzaki, M., Mizushima, S., Dohra, H., Ikegami, K., Yoshimura, T., Shiba, K., Inaba, K., & Sasanami, T.\n\n\n \n \n \n \n \n Sperm activation by heat shock protein 70 supports the migration of sperm released from sperm storage tubules in Japanese quail (Coturnix japonica).\n \n \n \n \n\n\n \n\n\n\n REPRODUCTION, 147(2): 167–178. February 2014.\n \n\n\n\n
\n\n\n\n \n \n \"SpermPaper\n  \n \n\n \n \n doi\n  \n \n\n \n link\n  \n \n\n bibtex\n \n\n \n  \n \n abstract \n \n\n \n\n \n \n \n \n \n \n \n\n  \n \n \n\n\n\n
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@article{hiyama_sperm_2014,\n\ttitle = {Sperm activation by heat shock protein 70 supports the migration of sperm released from sperm storage tubules in {Japanese} quail (\\textit{{Coturnix} japonica})},\n\tvolume = {147},\n\tissn = {1470-1626, 1741-7899},\n\turl = {https://rep.bioscientifica.com/view/journals/rep/147/2/167.xml},\n\tdoi = {10.1530/REP-13-0439},\n\tabstract = {Systems for maintaining the viability of ejaculated sperm in the female reproductive tract are widespread among vertebrates and invertebrates. In birds, this sperm storage function is performed by specialized simple tubular invaginations called sperm storage tubules (SSTs) in the uterovaginal junction (UVJ) of the oviduct. Although the incidence and physiological reasons for sperm storage in birds have been reported extensively, the mechanisms of sperm uptake by the SSTs, sperm maintenance within the SSTs, and control of sperm release from the SSTs are poorly understood. In this study, we demonstrated that the highly conserved heat shock protein 70 (HSP70) stimulates sperm motility\n              in vitro\n              and also that HSP70 expressed in the UVJ may facilitate the migration of sperm released from the SSTs. Quantitative RT-PCR analysis demonstrated that the expression of\n              HSP70\n              mRNA in the UVJ increases before ovulation/oviposition. Gene-specific\n              in situ\n              hybridization and immunohistochemical analysis with a specific antibody to HSP70 demonstrated that HSP70 is localized in the surface epithelium of the UVJ. Furthermore, injection of anti-HSP70 antibody into the vagina significantly inhibited fertilization\n              in vivo\n              . In addition, we found that recombinant HSP70 activates flagellar movement in the sperm and that the binding of recombinant HSP70 to the sperm surface is mediated through an interaction with voltage-dependent anion channel protein 2 (VDAC2). Our results suggest that HSP70 binds to the sperm surface by interacting with VDAC2 and activating sperm motility. This binding appears to play an important role in sperm migration within the oviduct.},\n\tnumber = {2},\n\turldate = {2021-07-27},\n\tjournal = {REPRODUCTION},\n\tauthor = {Hiyama, Gen and Matsuzaki, Mei and Mizushima, Shusei and Dohra, Hideo and Ikegami, Keisuke and Yoshimura, Takashi and Shiba, Kogiku and Inaba, Kazuo and Sasanami, Tomohiro},\n\tmonth = feb,\n\tyear = {2014},\n\tpages = {167--178},\n}\n\n
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\n Systems for maintaining the viability of ejaculated sperm in the female reproductive tract are widespread among vertebrates and invertebrates. In birds, this sperm storage function is performed by specialized simple tubular invaginations called sperm storage tubules (SSTs) in the uterovaginal junction (UVJ) of the oviduct. Although the incidence and physiological reasons for sperm storage in birds have been reported extensively, the mechanisms of sperm uptake by the SSTs, sperm maintenance within the SSTs, and control of sperm release from the SSTs are poorly understood. In this study, we demonstrated that the highly conserved heat shock protein 70 (HSP70) stimulates sperm motility in vitro and also that HSP70 expressed in the UVJ may facilitate the migration of sperm released from the SSTs. Quantitative RT-PCR analysis demonstrated that the expression of HSP70 mRNA in the UVJ increases before ovulation/oviposition. Gene-specific in situ hybridization and immunohistochemical analysis with a specific antibody to HSP70 demonstrated that HSP70 is localized in the surface epithelium of the UVJ. Furthermore, injection of anti-HSP70 antibody into the vagina significantly inhibited fertilization in vivo . In addition, we found that recombinant HSP70 activates flagellar movement in the sperm and that the binding of recombinant HSP70 to the sperm surface is mediated through an interaction with voltage-dependent anion channel protein 2 (VDAC2). Our results suggest that HSP70 binds to the sperm surface by interacting with VDAC2 and activating sperm motility. This binding appears to play an important role in sperm migration within the oviduct.\n
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\n \n\n \n \n Inaba, K., Mizuno, K., & Shiba, K.\n\n\n \n \n \n \n \n Structure, Function, and Phylogenetic Consideration of Calaxin.\n \n \n \n \n\n\n \n\n\n\n In Sawada, H., Inoue, N., & Iwano, M., editor(s), Sexual Reproduction in Animals and Plants, pages 49–57. Springer Japan, Tokyo, 2014.\n \n\n\n\n
\n\n\n\n \n \n \"Structure,Paper\n  \n \n\n \n \n doi\n  \n \n\n \n link\n  \n \n\n bibtex\n \n\n \n\n \n\n \n \n \n \n \n \n \n\n  \n \n \n\n\n\n
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@incollection{sawada_structure_2014,\n\taddress = {Tokyo},\n\ttitle = {Structure, {Function}, and {Phylogenetic} {Consideration} of {Calaxin}},\n\tisbn = {978-4-431-54588-0 978-4-431-54589-7},\n\turl = {http://link.springer.com/10.1007/978-4-431-54589-7_5},\n\tlanguage = {en},\n\turldate = {2021-07-27},\n\tbooktitle = {Sexual {Reproduction} in {Animals} and {Plants}},\n\tpublisher = {Springer Japan},\n\tauthor = {Inaba, Kazuo and Mizuno, Katsutoshi and Shiba, Kogiku},\n\teditor = {Sawada, Hitoshi and Inoue, Naokazu and Iwano, Megumi},\n\tyear = {2014},\n\tdoi = {10.1007/978-4-431-54589-7_5},\n\tpages = {49--57},\n}\n\n
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\n \n\n \n \n Kamiya, C., Ohta, N., Ogura, Y., Yoshida, K., Horie, T., Kusakabe, T. G., Satake, H., & Sasakura, Y.\n\n\n \n \n \n \n \n Nonreproductive role of gonadotropin-releasing hormone in the control of ascidian metamorphosis: FUNCTIONS OF GNRH IN ASCIDIANS.\n \n \n \n \n\n\n \n\n\n\n Developmental Dynamics, 243(12): 1524–1535. December 2014.\n \n\n\n\n
\n\n\n\n \n \n \"NonreproductivePaper\n  \n \n\n \n \n doi\n  \n \n\n \n link\n  \n \n\n bibtex\n \n\n \n\n \n\n \n \n \n \n \n \n \n\n  \n \n \n\n\n\n
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@article{kamiya_nonreproductive_2014,\n\ttitle = {Nonreproductive role of gonadotropin-releasing hormone in the control of ascidian metamorphosis: {FUNCTIONS} {OF} {GNRH} {IN} {ASCIDIANS}},\n\tvolume = {243},\n\tissn = {10588388},\n\tshorttitle = {Nonreproductive role of gonadotropin-releasing hormone in the control of ascidian metamorphosis},\n\turl = {https://onlinelibrary.wiley.com/doi/10.1002/dvdy.24176},\n\tdoi = {10.1002/dvdy.24176},\n\tlanguage = {en},\n\tnumber = {12},\n\turldate = {2021-07-27},\n\tjournal = {Developmental Dynamics},\n\tauthor = {Kamiya, Chisato and Ohta, Naoyuki and Ogura, Yosuke and Yoshida, Keita and Horie, Takeo and Kusakabe, Takehiro G. and Satake, Honoo and Sasakura, Yasunori},\n\tmonth = dec,\n\tyear = {2014},\n\tpages = {1524--1535},\n}\n
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\n \n\n \n \n Krupke, O., Yaguchi, S., Yaguchi, J., & Burke, R. D.\n\n\n \n \n \n \n \n Imaging Neural Development in Embryonic and Larval Sea Urchins.\n \n \n \n \n\n\n \n\n\n\n In Carroll, D. J., & Stricker, S. A., editor(s), Developmental Biology of the Sea Urchin and Other Marine Invertebrates, volume 1128, pages 147–160. Humana Press, Totowa, NJ, 2014.\n Series Title: Methods in Molecular Biology\n\n\n\n
\n\n\n\n \n \n \"ImagingPaper\n  \n \n\n \n \n doi\n  \n \n\n \n link\n  \n \n\n bibtex\n \n\n \n\n \n\n \n \n \n \n \n \n \n\n  \n \n \n\n\n\n
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@incollection{carroll_imaging_2014,\n\taddress = {Totowa, NJ},\n\ttitle = {Imaging {Neural} {Development} in {Embryonic} and {Larval} {Sea} {Urchins}},\n\tvolume = {1128},\n\tisbn = {978-1-62703-973-4 978-1-62703-974-1},\n\turl = {http://link.springer.com/10.1007/978-1-62703-974-1_9},\n\turldate = {2021-07-27},\n\tbooktitle = {Developmental {Biology} of the {Sea} {Urchin} and {Other} {Marine} {Invertebrates}},\n\tpublisher = {Humana Press},\n\tauthor = {Krupke, Oliver and Yaguchi, Shunsuke and Yaguchi, Junko and Burke, Robert D.},\n\teditor = {Carroll, David J. and Stricker, Stephen A.},\n\tyear = {2014},\n\tdoi = {10.1007/978-1-62703-974-1_9},\n\tnote = {Series Title: Methods in Molecular Biology},\n\tpages = {147--160},\n}\n\n
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\n \n\n \n \n Mizushima, S., Hiyama, G., Shiba, K., Inaba, K., Dohra, H., Ono, T., Shimada, K., & Sasanami, T.\n\n\n \n \n \n \n \n The birth of quail chicks after intracytoplasmic sperm injection.\n \n \n \n \n\n\n \n\n\n\n Development, 141(19): 3799–3806. October 2014.\n \n\n\n\n
\n\n\n\n \n \n \"ThePaper\n  \n \n\n \n \n doi\n  \n \n\n \n link\n  \n \n\n bibtex\n \n\n \n  \n \n abstract \n \n\n \n  \n \n 4 downloads\n \n \n\n \n \n \n \n \n \n \n\n  \n \n \n\n\n\n
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@article{mizushima_birth_2014,\n\ttitle = {The birth of quail chicks after intracytoplasmic sperm injection},\n\tvolume = {141},\n\tissn = {1477-9129, 0950-1991},\n\turl = {https://journals.biologists.com/dev/article/141/19/3799/46472/The-birth-of-quail-chicks-after-intracytoplasmic},\n\tdoi = {10.1242/dev.111765},\n\tabstract = {Intracytoplasmic sperm injection (ICSI) has been successfully used to produce offspring in several mammalian species including humans. However, ICSI has not been successful in birds because of the size of the egg and difficulty in mimicking the physiological polyspermy that takes place during normal fertilization. Microsurgical injection of 20 or more spermatozoa into an egg is detrimental to its survival. Here, we report that injection of a single spermatozoon with a small volume of sperm extract (SE) or its components led to the development and birth of healthy quail chicks. SE contains three factors – phospholipase Cζ (PLCZ), aconitate hydratase (AH) and citrate synthase (CS) – all of which are essential for full egg activation and subsequent embryonic development. PLCZ induces an immediate, transient Ca2+ rise required for the resumption of meiosis. AH and CS are required for long-lasting, spiral-like Ca2+ oscillations within the activated egg, which are essential for cell cycle progression in early embryos. We also found that co-injection of cRNAs encoding PLCZ, AH and CS support the full development of ICSI-generated zygotes without the use of SE. These findings will aid our understanding of the mechanism of avian fertilization and embryo development, as well as assisting in the manipulation of the avian genome and the production of transgenic and cloned birds.},\n\tlanguage = {en},\n\tnumber = {19},\n\turldate = {2021-07-27},\n\tjournal = {Development},\n\tauthor = {Mizushima, Shusei and Hiyama, Gen and Shiba, Kogiku and Inaba, Kazuo and Dohra, Hideo and Ono, Tamao and Shimada, Kiyoshi and Sasanami, Tomohiro},\n\tmonth = oct,\n\tyear = {2014},\n\tpages = {3799--3806},\n}\n\n
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\n Intracytoplasmic sperm injection (ICSI) has been successfully used to produce offspring in several mammalian species including humans. However, ICSI has not been successful in birds because of the size of the egg and difficulty in mimicking the physiological polyspermy that takes place during normal fertilization. Microsurgical injection of 20 or more spermatozoa into an egg is detrimental to its survival. Here, we report that injection of a single spermatozoon with a small volume of sperm extract (SE) or its components led to the development and birth of healthy quail chicks. SE contains three factors – phospholipase Cζ (PLCZ), aconitate hydratase (AH) and citrate synthase (CS) – all of which are essential for full egg activation and subsequent embryonic development. PLCZ induces an immediate, transient Ca2+ rise required for the resumption of meiosis. AH and CS are required for long-lasting, spiral-like Ca2+ oscillations within the activated egg, which are essential for cell cycle progression in early embryos. We also found that co-injection of cRNAs encoding PLCZ, AH and CS support the full development of ICSI-generated zygotes without the use of SE. These findings will aid our understanding of the mechanism of avian fertilization and embryo development, as well as assisting in the manipulation of the avian genome and the production of transgenic and cloned birds.\n
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\n \n\n \n \n Nakano, H.\n\n\n \n \n \n \n \n Survey of the Japanese Coast Reveals Abundant Placozoan Populations in the Northern Pacific Ocean.\n \n \n \n \n\n\n \n\n\n\n Scientific Reports, 4(1): 5356. 2014.\n \n\n\n\n
\n\n\n\n \n \n \"SurveyPaper\n  \n \n\n \n \n doi\n  \n \n\n \n link\n  \n \n\n bibtex\n \n\n \n\n \n\n \n \n \n \n \n \n \n\n  \n \n \n\n\n\n
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@article{nakano_survey_2014,\n\ttitle = {Survey of the {Japanese} {Coast} {Reveals} {Abundant} {Placozoan} {Populations} in the {Northern} {Pacific} {Ocean}},\n\tvolume = {4},\n\tissn = {2045-2322},\n\turl = {http://www.nature.com/articles/srep05356},\n\tdoi = {10.1038/srep05356},\n\tlanguage = {en},\n\tnumber = {1},\n\turldate = {2021-07-27},\n\tjournal = {Scientific Reports},\n\tauthor = {Nakano, Hiroaki},\n\tyear = {2014},\n\tpages = {5356},\n}\n\n
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\n \n\n \n \n Sasaki, H., Yoshida, K., Hozumi, A., & Sasakura, Y.\n\n\n \n \n \n \n \n CRISPR/Cas9-mediated gene knockout in the ascidian Ciona intestinalis.\n \n \n \n \n\n\n \n\n\n\n Development, Growth & Differentiation, 56(7): 499–510. September 2014.\n \n\n\n\n
\n\n\n\n \n \n \"CRISPR/Cas9-mediatedPaper\n  \n \n\n \n \n doi\n  \n \n\n \n link\n  \n \n\n bibtex\n \n\n \n\n \n\n \n \n \n \n \n \n \n\n  \n \n \n\n\n\n
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@article{sasaki_crisprcas9-mediated_2014,\n\ttitle = {{CRISPR}/{Cas9}-mediated gene knockout in the ascidian \\textit{{Ciona} intestinalis}},\n\tvolume = {56},\n\tissn = {0012-1592, 1440-169X},\n\tshorttitle = {{\\textless}span style="font-variant},\n\turl = {https://onlinelibrary.wiley.com/doi/10.1111/dgd.12149},\n\tdoi = {10.1111/dgd.12149},\n\tlanguage = {en},\n\tnumber = {7},\n\turldate = {2021-07-27},\n\tjournal = {Development, Growth \\& Differentiation},\n\tauthor = {Sasaki, Haruka and Yoshida, Keita and Hozumi, Akiko and Sasakura, Yasunori},\n\tmonth = sep,\n\tyear = {2014},\n\tpages = {499--510},\n}\n\n
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\n \n\n \n \n Sasakura, Y.\n\n\n \n \n \n \n \n Germline Transformation in the Ascidian Ciona intestinalis.\n \n \n \n \n\n\n \n\n\n\n In Sawada, H., Inoue, N., & Iwano, M., editor(s), Sexual Reproduction in Animals and Plants, pages 465–473. Springer Japan, Tokyo, 2014.\n \n\n\n\n
\n\n\n\n \n \n \"GermlinePaper\n  \n \n\n \n \n doi\n  \n \n\n \n link\n  \n \n\n bibtex\n \n\n \n\n \n\n \n \n \n \n \n \n \n\n  \n \n \n\n\n\n
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@incollection{sawada_germline_2014,\n\taddress = {Tokyo},\n\ttitle = {Germline {Transformation} in the {Ascidian} \\textit{{Ciona} intestinalis}},\n\tisbn = {978-4-431-54588-0 978-4-431-54589-7},\n\turl = {http://link.springer.com/10.1007/978-4-431-54589-7_38},\n\tlanguage = {en},\n\turldate = {2021-07-27},\n\tbooktitle = {Sexual {Reproduction} in {Animals} and {Plants}},\n\tpublisher = {Springer Japan},\n\tauthor = {Sasakura, Yasunori},\n\teditor = {Sawada, Hitoshi and Inoue, Naokazu and Iwano, Megumi},\n\tyear = {2014},\n\tdoi = {10.1007/978-4-431-54589-7_38},\n\tpages = {465--473},\n}\n\n
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\n \n\n \n \n Shiba, K., & Inaba, K.\n\n\n \n \n \n \n \n Distinct Roles of Soluble and Transmembrane Adenylyl Cyclases in the Regulation of Flagellar Motility in Ciona Sperm.\n \n \n \n \n\n\n \n\n\n\n International Journal of Molecular Sciences, 15(8): 13192–13208. July 2014.\n \n\n\n\n
\n\n\n\n \n \n \"DistinctPaper\n  \n \n\n \n \n doi\n  \n \n\n \n link\n  \n \n\n bibtex\n \n\n \n\n \n\n \n \n \n \n \n \n \n\n  \n \n \n\n\n\n
\n
@article{shiba_distinct_2014,\n\ttitle = {Distinct {Roles} of {Soluble} and {Transmembrane} {Adenylyl} {Cyclases} in the {Regulation} of {Flagellar} {Motility} in \\textit{{Ciona}} {Sperm}},\n\tvolume = {15},\n\tissn = {1422-0067},\n\turl = {http://www.mdpi.com/1422-0067/15/8/13192},\n\tdoi = {10.3390/ijms150813192},\n\tlanguage = {en},\n\tnumber = {8},\n\turldate = {2021-07-27},\n\tjournal = {International Journal of Molecular Sciences},\n\tauthor = {Shiba, Kogiku and Inaba, Kazuo},\n\tmonth = jul,\n\tyear = {2014},\n\tpages = {13192--13208},\n}\n\n
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\n \n\n \n \n Sung, C., Kim, T. W., Park, Y., Kang, S., Inaba, K., Shiba, K., Choi, T. S., Moon, S., Litvin, S., Lee, K., & Lee, J.\n\n\n \n \n \n \n \n Species and gamete-specific fertilization success of two sea urchins under near future levels of pCO$_{\\textrm{2}}$.\n \n \n \n \n\n\n \n\n\n\n Journal of Marine Systems, 137: 67–73. September 2014.\n \n\n\n\n
\n\n\n\n \n \n \"SpeciesPaper\n  \n \n\n \n \n doi\n  \n \n\n \n link\n  \n \n\n bibtex\n \n\n \n\n \n\n \n \n \n \n \n \n \n\n  \n \n \n\n\n\n
\n
@article{sung_species_2014,\n\ttitle = {Species and gamete-specific fertilization success of two sea urchins under near future levels of {pCO}$_{\\textrm{2}}$},\n\tvolume = {137},\n\tissn = {09247963},\n\turl = {https://linkinghub.elsevier.com/retrieve/pii/S0924796314000992},\n\tdoi = {10.1016/j.jmarsys.2014.04.013},\n\tlanguage = {en},\n\turldate = {2021-07-27},\n\tjournal = {Journal of Marine Systems},\n\tauthor = {Sung, Chan-Gyung and Kim, Tae Won and Park, Young-Gyu and Kang, Seong-Gil and Inaba, Kazuo and Shiba, Kogiku and Choi, Tae Seob and Moon, Seong-Dae and Litvin, Steve and Lee, Kyu-Tae and Lee, Jung-Suk},\n\tmonth = sep,\n\tyear = {2014},\n\tpages = {67--73},\n}\n\n
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\n \n\n \n \n Treen, N., Yoshida, K., Sakuma, T., Sasaki, H., Kawai, N., Yamamoto, T., & Sasakura, Y.\n\n\n \n \n \n \n \n Tissue-specific and ubiquitous gene knockouts by TALEN electroporation provide new approaches to investigating gene function in Ciona.\n \n \n \n \n\n\n \n\n\n\n Development, 141(2): 481–487. January 2014.\n \n\n\n\n
\n\n\n\n \n \n \"Tissue-specificPaper\n  \n \n\n \n \n doi\n  \n \n\n \n link\n  \n \n\n bibtex\n \n\n \n  \n \n abstract \n \n\n \n\n \n \n \n \n \n \n \n\n  \n \n \n\n\n\n
\n
@article{treen_tissue-specific_2014,\n\ttitle = {Tissue-specific and ubiquitous gene knockouts by {TALEN} electroporation provide new approaches to investigating gene function in \\textit{{Ciona}}},\n\tvolume = {141},\n\tissn = {1477-9129, 0950-1991},\n\turl = {https://journals.biologists.com/dev/article/141/2/481/46452/Tissue-specific-and-ubiquitous-gene-knockouts-by},\n\tdoi = {10.1242/dev.099572},\n\tabstract = {Custom designed nucleases can simplify gene targeting experiments and have the potential to allow these techniques to be performed in a wide range of organisms. Transcriptional activator-like effector nucleases (TALENs) are starting to fulfill this potential with the advantages of low cost and fast construction times. Here, we report that TALENs are highly effective at inducing mutations in specific genomic loci in the ascidian chordate Ciona intestinalis. In Ciona there are well-established methods to introduce exogenous DNA by electroporation, and we show that this method can be used to introduce constructs that can express TALENs ubiquitously or in specific tissues. Our current protocols enable the rapid analysis of hundreds of TALEN-induced mutants. TALEN electroporations result in a high rate of mutations. These mutations can result in gene knockouts that recapitulate previously described functions of Fgf3 and Hox12. We show that TALENs can work efficiently to cause tissue-specific knockouts and demonstrate this by knocking out Hox12 in the epidermis and Fgf3 in neural tissues. We also use tissue-specific knockouts to reveal a new function of Fgf3 during ascidian larval metamorphosis.},\n\tlanguage = {en},\n\tnumber = {2},\n\turldate = {2021-07-27},\n\tjournal = {Development},\n\tauthor = {Treen, Nicholas and Yoshida, Keita and Sakuma, Tetsushi and Sasaki, Haruka and Kawai, Narudo and Yamamoto, Takashi and Sasakura, Yasunori},\n\tmonth = jan,\n\tyear = {2014},\n\tpages = {481--487},\n}\n\n
\n
\n\n\n
\n Custom designed nucleases can simplify gene targeting experiments and have the potential to allow these techniques to be performed in a wide range of organisms. Transcriptional activator-like effector nucleases (TALENs) are starting to fulfill this potential with the advantages of low cost and fast construction times. Here, we report that TALENs are highly effective at inducing mutations in specific genomic loci in the ascidian chordate Ciona intestinalis. In Ciona there are well-established methods to introduce exogenous DNA by electroporation, and we show that this method can be used to introduce constructs that can express TALENs ubiquitously or in specific tissues. Our current protocols enable the rapid analysis of hundreds of TALEN-induced mutants. TALEN electroporations result in a high rate of mutations. These mutations can result in gene knockouts that recapitulate previously described functions of Fgf3 and Hox12. We show that TALENs can work efficiently to cause tissue-specific knockouts and demonstrate this by knocking out Hox12 in the epidermis and Fgf3 in neural tissues. We also use tissue-specific knockouts to reveal a new function of Fgf3 during ascidian larval metamorphosis.\n
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\n \n\n \n \n Yokoe, M., Sano, M., Shibata, H., Shibata, D., Takayama-Watanabe, E., Inaba, K., & Watanabe, A.\n\n\n \n \n \n \n \n Sperm Proteases that May Be Involved in the Initiation of Sperm Motility in the Newt, Cynops pyrrhogaster.\n \n \n \n \n\n\n \n\n\n\n International Journal of Molecular Sciences, 15(9): 15210–15224. August 2014.\n \n\n\n\n
\n\n\n\n \n \n \"SpermPaper\n  \n \n\n \n \n doi\n  \n \n\n \n link\n  \n \n\n bibtex\n \n\n \n\n \n\n \n \n \n \n \n \n \n\n  \n \n \n\n\n\n
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@article{yokoe_sperm_2014,\n\ttitle = {Sperm {Proteases} that {May} {Be} {Involved} in the {Initiation} of {Sperm} {Motility} in the {Newt}, \\textit{{Cynops} pyrrhogaster}},\n\tvolume = {15},\n\tissn = {1422-0067},\n\turl = {http://www.mdpi.com/1422-0067/15/9/15210},\n\tdoi = {10.3390/ijms150915210},\n\tlanguage = {en},\n\tnumber = {9},\n\turldate = {2021-07-27},\n\tjournal = {International Journal of Molecular Sciences},\n\tauthor = {Yokoe, Misato and Sano, Makoto and Shibata, Honami and Shibata, Daisuke and Takayama-Watanabe, Eriko and Inaba, Kazuo and Watanabe, Akihiko},\n\tmonth = aug,\n\tyear = {2014},\n\tpages = {15210--15224},\n}\n\n
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\n \n\n \n \n Yoshida, K., Treen, N., Hozumi, A., Sakuma, T., Yamamoto, T., & Sasakura, Y.\n\n\n \n \n \n \n \n Germ cell mutations of the ascidian Ciona intestinalis with TALE nucleases: germ cell mutagenesis in ciona.\n \n \n \n \n\n\n \n\n\n\n genesis, 52(5): 431–439. May 2014.\n \n\n\n\n
\n\n\n\n \n \n \"GermPaper\n  \n \n\n \n \n doi\n  \n \n\n \n link\n  \n \n\n bibtex\n \n\n \n\n \n\n \n \n \n \n \n \n \n\n  \n \n \n\n\n\n
\n
@article{yoshida_germ_2014,\n\ttitle = {Germ cell mutations of the ascidian \\textit{{Ciona} intestinalis} with {TALE} nucleases: germ cell mutagenesis in \\textit{ciona}},\n\tvolume = {52},\n\tissn = {1526954X},\n\tshorttitle = {Germ cell mutations of the ascidian \\textit{{Ciona} intestinalis} with {TALE} nucleases},\n\turl = {https://onlinelibrary.wiley.com/doi/10.1002/dvg.22770},\n\tdoi = {10.1002/dvg.22770},\n\tlanguage = {en},\n\tnumber = {5},\n\turldate = {2021-07-27},\n\tjournal = {genesis},\n\tauthor = {Yoshida, Keita and Treen, Nicholas and Hozumi, Akiko and Sakuma, Tetsushi and Yamamoto, Takashi and Sasakura, Yasunori},\n\tmonth = may,\n\tyear = {2014},\n\tpages = {431--439},\n}\n\n
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\n \n\n \n \n 今孝悦, Khrueniam, U., 有元貴文, 吉川尚, 岡本侑樹, & 石川智士\n\n\n \n \n \n \n \n 1. タイ・ラヨーン沿岸における定置網漁獲物の栄養段階.\n \n \n \n \n\n\n \n\n\n\n 日本水産学会誌, 80(5): 837–837. 2014.\n Publisher: 公益社団法人 日本水産学会\n\n\n\n
\n\n\n\n \n \n \"1.Paper\n  \n \n\n \n\n \n link\n  \n \n\n bibtex\n \n\n \n  \n \n abstract \n \n\n \n\n \n \n \n \n \n \n \n\n  \n \n \n\n\n\n
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@article{_1_2014,\n\ttitle = {1. タイ・ラヨーン沿岸における定置網漁獲物の栄養段階},\n\tvolume = {80},\n\tissn = {0021-5392},\n\turl = {https://ci.nii.ac.jp/naid/130004694420},\n\tabstract = {1. タイ・ラヨーン沿岸における定置網漁獲物の栄養段階 今 孝悦 , KHRUENIAM UDOM , 有元 貴文 , 吉川 尚 , 岡本 侑樹 , 石川 智士 日本水産学会誌 80(5), 837-837, 2014},\n\tlanguage = {en},\n\tnumber = {5},\n\turldate = {2021-07-27},\n\tjournal = {日本水産学会誌},\n\tauthor = {{今孝悦} and Khrueniam, Udom and {有元貴文} and {吉川尚} and {岡本侑樹} and {石川智士}},\n\tyear = {2014},\n\tnote = {Publisher: 公益社団法人 日本水産学会},\n\tpages = {837--837},\n}\n\n
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\n 1. タイ・ラヨーン沿岸における定置網漁獲物の栄養段階 今 孝悦 , KHRUENIAM UDOM , 有元 貴文 , 吉川 尚 , 岡本 侑樹 , 石川 智士 日本水産学会誌 80(5), 837-837, 2014\n
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\n \n\n \n \n 伊川正人\n\n\n \n \n \n \n 特集受精メカニズム新論争-ドグマの再構築.\n \n \n \n\n\n \n\n\n\n 学研メディカル秀潤社, 東京, 2014.\n OCLC: 874519589\n\n\n\n
\n\n\n\n \n\n \n\n \n link\n  \n \n\n bibtex\n \n\n \n\n \n\n \n \n \n \n \n \n \n\n  \n \n \n\n\n\n
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@book{_-_2014,\n\taddress = {東京},\n\ttitle = {特集受精メカニズム新論争-ドグマの再構築},\n\tisbn = {978-4-7809-0153-5},\n\tlanguage = {Japanese},\n\tpublisher = {学研メディカル秀潤社},\n\tauthor = {{伊川正人}},\n\tyear = {2014},\n\tnote = {OCLC: 874519589},\n}\n\n
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\n \n\n \n \n 山本卓\n\n\n \n \n \n \n 今すぐ始めるゲノム編集: TALEN&CRISPR/Cas9の必須知識と実験プロトコール.\n \n \n \n\n\n \n\n\n\n 羊土社, 東京, 2014.\n OCLC: 875128657\n\n\n\n
\n\n\n\n \n\n \n\n \n link\n  \n \n\n bibtex\n \n\n \n\n \n\n \n \n \n \n \n \n \n\n  \n \n \n\n\n\n
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@book{__2014,\n\taddress = {東京},\n\ttitle = {今すぐ始めるゲノム編集: {TALEN}\\&{CRISPR}/{Cas9の必須知識と実験プロトコール}},\n\tisbn = {978-4-7581-0190-5},\n\tshorttitle = {今すぐ始めるゲノム編集},\n\tlanguage = {Japanese},\n\tpublisher = {羊土社},\n\tauthor = {{山本卓}},\n\tyear = {2014},\n\tnote = {OCLC: 875128657},\n}\n\n
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\n \n\n \n \n 岡本侑樹, 石川智士, 今孝悦, 渡邉一哉, 吉川尚, & Salaenoi, J.\n\n\n \n \n \n \n \n 2. タイ南部バンドン湾の貝類養殖域における食物網構造.\n \n \n \n \n\n\n \n\n\n\n 日本水産学会誌, 80(5): 838–838. 2014.\n Publisher: 公益社団法人 日本水産学会\n\n\n\n
\n\n\n\n \n \n \"2.Paper\n  \n \n\n \n\n \n link\n  \n \n\n bibtex\n \n\n \n  \n \n abstract \n \n\n \n\n \n \n \n \n \n \n \n\n  \n \n \n\n\n\n
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@article{_2_2014,\n\ttitle = {2. タイ南部バンドン湾の貝類養殖域における食物網構造},\n\tvolume = {80},\n\tissn = {0021-5392},\n\turl = {https://ci.nii.ac.jp/naid/130004694421},\n\tabstract = {2. タイ南部バンドン湾の貝類養殖域における食物網構造 岡本 侑樹 , 石川 智士 , 今 孝悦 , 渡邉 一哉 , 吉川 尚 , SALAENOI JINTANA 日本水産学会誌 80(5), 838-838, 2014},\n\tlanguage = {en},\n\tnumber = {5},\n\turldate = {2021-07-27},\n\tjournal = {日本水産学会誌},\n\tauthor = {{岡本侑樹} and {石川智士} and {今孝悦} and {渡邉一哉} and {吉川尚} and Salaenoi, Jintana},\n\tyear = {2014},\n\tnote = {Publisher: 公益社団法人 日本水産学会},\n\tpages = {838--838},\n}\n\n
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\n 2. タイ南部バンドン湾の貝類養殖域における食物網構造 岡本 侑樹 , 石川 智士 , 今 孝悦 , 渡邉 一哉 , 吉川 尚 , SALAENOI JINTANA 日本水産学会誌 80(5), 838-838, 2014\n
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\n \n\n \n \n 沢田 均\n\n\n \n \n \n \n 動植物の受精学: 共通機構と多様性.\n \n \n \n\n\n \n\n\n\n 化学同人, 京都, 2014.\n OCLC: 882595519\n\n\n\n
\n\n\n\n \n\n \n\n \n link\n  \n \n\n bibtex\n \n\n \n\n \n\n \n \n \n \n \n \n \n\n  \n \n \n\n\n\n
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@book{___2014,\n\taddress = {京都},\n\ttitle = {動植物の受精学: 共通機構と多様性},\n\tisbn = {978-4-7598-1514-6},\n\tshorttitle = {動植物の受精学},\n\tlanguage = {Japanese},\n\tpublisher = {化学同人},\n\tauthor = {{沢田 均}},\n\tyear = {2014},\n\tnote = {OCLC: 882595519},\n}\n\n
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