148 Izutsu, K., Fujimaki, Y., Kuwabara, A. and Aoyagi, N.: Effect of Counterions on the Physical Properties of L- Arginine in Fr

Total Page:16

File Type:pdf, Size:1020Kb

148 Izutsu, K., Fujimaki, Y., Kuwabara, A. and Aoyagi, N.: Effect of Counterions on the Physical Properties of L- Arginine in Fr 148 国 立 衛 研 報 第124号(2006) 誌 上 発 表(原著論文) Summaries of Papers Published in Other Journals (Original Papers) Izutsu, K., Fujimaki, Y., Kuwabara, A. and Aoyagi, N.: 檜山行雄:品質に関するトピックの動向-Q9- Effect of counterions on the physical properties of L- 医薬品研究,37(2),131-139(2006). arginine in frozen solutions and freeze-dried solids. Keywords: ICH, risk management, pharmaceutical quality Int. J. Pharm., 301, 161-169 (2005). Keywords: freeze-drying, molecular interaction, Tagawa, H.*, Kizuka, Y.*, Ikeda, T.*, Itoh, S., Kawasaki, amorphous, formulation N., Kurihara, H.*, Onozato, H.*, Tojo, A.*, Sakai, T.*, Kawasaki, T.* and Oka, S.*: A non-sulfated from of the Izutsu, K., Fujimaki, Y., Kuwabara, A., Hiyama, Y., NHK-1 carbohydrate is specifically expressed in mouse Yomota, C. and Aoyagi, N.: Near-infrared analysis of kidney. protein secondary structure in aqueous solutions and J. Biol. Chem., 280, 23876-23883 (2005). freeze-dried solids. Keywords: HNK-1, glucuronyltransferases, CD13/ J. Pharm. Sci., 95, 781-789 (2006). aminopeptidase N Keywords: freeze-drying, secondary structure, near- *京都大学大学院 infrared spectroscopy, protein formulation Hirano, M.*, Ma, B. Y.*, Kawasaki, N., Okimura, K.*, Yoshioka, S., Aso, Y. and Miyazaki, T.: Negligible Baba, M.*, Nakagawa, T.*, Miwa, K.*, Kawasaki, N.*, contribution of molecular mobility to the degradation Oka, S.* and Kawasaki, T.*: Mannan-binding (and rate of insulin lyophilized with poly(vinylpyrrolidone). (protein blocks the activation of metalloproteases J. Pharm. Sci., 95, 939-643 (2006). meprin. Keywords: solid state stability, glass transition, molecular J. Immunol., 175, 3177-3185 (2005). mobility Keywords: meprin, mannan-binding protein, MBP ligands *京都大学大学院 Yoshioka, S. and Aso, Y.: Comparison of the glass transition temperature and fragility parameter of Hashii, N., Kawasaki, N., Itoh, S., Hyuga, M., isomalto-olygomer predicted by molecular dynamics Kawanishi, T. and Hayakawa, T.: Glycomic/ simulations with those measured by differential scanning glycoproteomic analysis by LC/MS: Analysis of glycan calorimetry. structural alternation in the cells. Chem. Pharm. Bull., 53, 1443-1445 (2005). Proteomics, 5, 4665-4672 (2005). Keywords: molecular dynamics simulation, glass transition, Keywords: LC/MS, N-acetylglucosaminyltransferase III, fragility oligosaccharide Yoshioka, S. and Aso, Y.: A quantitative assessment of Itoh, S., Kawasaki, N., Harazono, A., Hashii, N., Matsuishi, the significance of molecular mobility as a determinant Y., Kawanishi, T. and Hayakawa, T.: Characterization of for the stability of lyophilized insulin formulations. a gel-separated unknown glycoprotein by liquid Pharm. Res., 22, 1358-1364 (2005). chromatography/ multiple tandem mass spectrometry. Keywords: molecular mobility, glass transition temperature, Analysis of rat brain Thy-1 separated by sodium insulin dodecyl sulfate-polyacrylamide gel electrophoresis. J. Chromatogr. A, 1094, 105-1017 (2005). Aso, Y. and Yoshioka, S: Molecular Mobility of Nifedipine- Keywords: LC/MS, SDS-PAGE, Thy-1 PVP and Phenobarbital-PVP Solid Dispersions as Measured by 13C-NMR Spin-Lattice Relaxation Time. Itoh, S., Kawasaki, N., Hashii, N., Harazono, A., J. Pharm. Sci., 95, 318-325 (2006). Matsuishi, Y., Hayakawa, T. and Kawanishi, T.: N-linked Keywords: Spin-lattice relaxation time, Solid dispersion, oligosaccharide analysis by liquid chromatography with Stability graphitized carbon column/ liner ion trap-Fourier transform ion cyclotron resonance mass spectrometry in 小山靖人,檜山行雄:医薬品製剤 GMP ガイドライン- positive and negative ion modes. これからの GMP のあるべき姿と国際調和 J. Chromatogr. A, 1103, 296-306 (2006). PHARMA TECH JAPAN, 21, 1365-1376 (2005). Keywords: LC/MS, FT-ICR-MS, Thy-1 Keywords: GMP, guideline, pharmaceutical quality Harazono, A., Kawasaki, N., Itoh, S., Hashii, N., Ishii- 檜山行雄,坂本知昭:GMP をめぐる動向について Watabe, A., Kawanish, T. and Hayakawa, T: Site-specific 医薬品研究,37(1),42-56(2006). N-glycosylation analysis of human plasma cerulopasmin Keywords: pharmaceutical quality, GMP, ICH using liquid chromatography/ electrospry ionization tandem mass spectrometry. 誌 上 発 表(原著論文) 149 Anal. Biochem., 348, 259-268 (2006). Ebizuka, Y.* and Goda, Y.: Inhibition of human Keywords: LC/MS, ceruloplasmin, site-specific glycosylation lanosterol synthase by constituents of Laurus nobilis L. analysis Journal of Natural Medicines, 60, 78-81 (2006). Keywords: Laurus nobilis, lanosterol synthase inhibition, Hashii, N., Kawasaki, N., Itoh, S., Harazono, A., bay leaf Matsuishi, Y., Hayakawa, T. and Kawanishi, T.: Specific *東大院薬 detection of Lewis x-carbohydrates in biological samples using liquid chromatography/multiple-stage tandem Shoji, T.*, Masumoto, S.*, Moriichi, N.*, Akiyama, H., mass spectrometry. Kanda, T.*, Ohtake, Y.*, Goda, Y.: Apple procyanidin Rapid commun. Mass spectrom., 19, 3315-3321 (2005). oligomers absorption in rats after oral administration: Keywords: LC/MS, Lewis x, oligosaccharide analysis of procyanidins in plasma using the Porter method and high-performance liquid chromatography/ Niimi, S., Harashima, M.*, Takayama, K.*, Hara, M.*, tandem mass spectrometry. Hyuga, M., Seki, T.*, Ariga, T.*, Kawanishi, T. and J. Agric. Food Chem., 54, 884-892 (2005). Hayakawa, T.: Thrombomodulin enhances the invasive Keywords: absorption, apple procyanaidins, HPLC/MS/ activity of mouse mammary tumor cells. MS J. Biochem., 137, 579-586 (2005). *アサヒビール基盤研究所 Keywords: thrombomodulin, thrombin, invasion *日本大学生物資源科学部 Tanaka, R.*, Morimoto, T.*, Nakamura, M.* and Goda, Y.: Component determination and specification of a 後藤洋子*,新見伸吾:ラクトース修飾絹フィブロイ food additives, “Methyl Hesperidin”. ン基材上の初代培養ラット肝細胞の形態および機能に Japanese Journal of Food Chemistry, 12, 71-75 (2005). 及ぼすインスリンとデキサメタゾンの作用 Keywords: hesperidin, hesperetin, flavonoid 高分子論文集(Kobunshi Ronbunshu),62(7),326- *三栄源FFI 330(2005). Keywords: Lactose-Silk Fibroin conjugates, Rat hepatocytes, Uchiyama, N., Kim, I. H., Kawahara, N. and Goda, Y.: Morphology HPLC separation of hesperidin and the C-2 epimer in *農業生物資源研究所 commercial hesperidin samples and herbal medicines. Chirality, 17, 373-377 (2005). Kumagai, Y.*, Hyuga, S.*, Hyuga, M., Watanabe, K.*, Keywords: hesperidin, diastereomer separation, online Kawanishi, T. and Hanawa, T.*: Estrogen-like activity CD detection in Kampo medicines used for menopausal symptoms and gynecological diseases. Sato, M.*, Anetai, M.* and Goda, Y.: Oraganophosphorus J. Trad. Med., 22, 228-236 (2005). pesticide residues in decoctions of crude drugs. Keywords: estrogen, menopausal symptoms, gynecological Iyakuhin Kenkyu, 37, 245-250 (2006). diseases Keywords: organophosphorus pesticide residues, *北里研究所東洋医学総合研究所 decoction, Kampo extracts *北海道立衛生研究所 Tanaka, H.*, Namekata, I.*, Takeda, K.*, Kazama, A.*, Shimizu, Y.*, Moriwaki, R.*, Hirayama, W.*, Sato, A.*, Kinoshita, T.*, Haga, Y.*, Narimatsu, S.*, Shimada, M.* Kawanishi, T. and Shigenobu, K.*: Unique excitation - and Goda, Y.: The isolation and structure elucidation of contraction characteristics of mouse myocardium as new cassane diterpene-acids from Caesalpinia crista L. revealed by SEA0400, a specific inhibitor of Na+-Ca2+ (Fabaceae), and review on nomenclature of some exchanger. Caesalpinia species. Naunyn Schmiedebergs Arch. Pharmacol., 371, 526-534 Chem Pharm. Bull., 53, 717-720 (2005). (2005). Keywords: Caesalpinia crista, Fabaceae, cassane diterpene Keywords: sodium, calcium, myocardium *帝京大学薬学部 *東邦大学薬学部 Yamamoto, K.*, Yamamoto, T.*, Kondo, S.*, Tamura, Kawanishi, T.: Regulatory perspectives from Japan - M.*, Shibata, Y.*, Umeda, K.*, Akiba, S.*, Kawakami, comparability of biopharmaceuticals. T.*, Saito, F.*, Sugimoto, T.*, Nakashima, Y.*, Biologicals, 34, 65-68 (2006). Tahara, M., Hayashi, K.*, Sudo, M.*, Nakanishi, K.*, Keywords: regulation, biopharmaceuticals, comparability Isozaki, O.*, Kawahara, N. and Goda, Y.: Assay of ginsenoside Rg1 and ginsenoside Rb1 in Ginseng and Red Tanaka, R., Sakano, Y.*, Shimizu, K., Shibuya, M.*, Ginseng by high-performance liquid chromatography. 150 国 立 衛 研 報 第124号(2006) Iyakuhin Kenkyu, 36, 211-222 (2005). Kuroyanagi, M.*1, Shimomae, M.*1, Nagashima, Y.*1, Keywords: ginsenoside quantification method, Japanese Muto, N.*1, Okuda, T.*1, Kawahara, N., Nakane, T.*2 Pharmacopoeia, validation data and Sano, T.*3: New Diarylheptanoids from Alnus *日本漢方生薬製剤協会 japonica and Their Antioxidative Activity. Chem. Pharm. Bull., 53 (12), 1519-1523 (2005). Saito, K.*, Toyo'oka, T.*, Kato, M.*, Fukushima, T.*, Keywords: Alnus japonica, Betulaceae, diarylheptanoid Shirota, O. and Goda, Y.: Determination of psilocybin in *1 広島県立大学 hallucinogenic mushrooms by reversed-phase liquid *2 昭和薬科大学 chromatography with fluorescence detection. *3 広島県林業センター Talanta, 66, 562-568 (2005). *静岡県立大学薬学部 Kim, I-H., Kaneko, N., Uchiyama, N., Lee, J-E.*, Takeya, K.*, Kawahara, N. and Goda, Y.: Two phenylpropanoid Sasaki, N.*, Abe, Y.*, Wada, K.*, Koda, T.*, Goda, Y., glycosides from Neopicrorhiza scrophulariiflora. Adachi, T.* and Ozeki, Y.*: Amaranthin in geather Chem. Pharm. Bull., 54 (2), 275-277 (2006). cockscombs is synthesized via glucuronylation at the Keywords: Neopicrorhiza scrophulariiflora, Scrophularia- cyclo-DOPA glucoside step in the betacyanin biosynthetic ceae, phenylpropanoid glycoside pathway. *東京薬科大学 J. Plant Res., 118, 439-442 (2005). Keywords: amaranthin, betacyanin biosynthetic pahway, Otsuki, T.*1, Sato, M.*1, Kayano, T.*2, Kowithayakorn, cyclo-DOPA glucoside step T.*3, Kawahara, N., Goda, Y. and Ishibashi, M.*1: *東京農工大学工学部生命工学科 Steroidal saponins from Calamus insignis, and their cell growth and cell cycle inhibitory activities. Anjiki,
Recommended publications
  • Regulation of Cardiac Progenitors by Combination of Mesp1 and ETS
    REGULATION OF CARDIAC PROGENITORS BY COMBINATION OF MESP1 AND ETS TRANSCRIPTION FACTORS A Dissertation by KUO-CHAN WENG Submitted to the Office of Graduate and Professional Studies of Texas A&M University in partial fulfillment of the requirements for the degree of DOCTOR OF PHILOSOPHY Chair of Committee, Fen Wang Co-Chair of Committee, Robert J. Schwartz Committee Members, James F. Martin Jiang Chang Head of Department, Fen Wang May 2014 Major Subject: Medical Science Copyright 2014 Kuo-Chan Weng ABSTRACT Heart disease remains the leading cause of death worldwide. By understanding the regulating networks during cardiac development we can exploit those networks to manipulate adult cells into cardiac progenitors and provide an alternative for repairing diseased hearts. Mesp1 is considered to have critical roles during cardiac development but the molecular mechanisms need to be further studied. The roles of ETS transcription factors have been primarily limited to hematopoietic differentiation and cancer progression. The ETS transcription factors are known to have proliferating roles and were hypothesized to also be involved in cardiac differentiation and may potentially be used for cell reprogramming. The first part of this study characterizes the expression pattern of Mesp1 protein in early mouse embryo from E6.5 to E9.5 and provides a full expression profile in differentiating embryoid bodies in vitro from the undifferentiated stage to Day10. Our work showed Mesp1 expresses in the posterior region of E6.5 embryo then starts migrating through the primitive streak toward anterior mesoderm and endoderm in E7.5. A Mesp1 linage tracing ES cell line was established, and it allowed us to trace the Mesp1 derived cell population.
    [Show full text]
  • Detailed Review Paper on Retinoid Pathway Signalling
    1 1 Detailed Review Paper on Retinoid Pathway Signalling 2 December 2020 3 2 4 Foreword 5 1. Project 4.97 to develop a Detailed Review Paper (DRP) on the Retinoid System 6 was added to the Test Guidelines Programme work plan in 2015. The project was 7 originally proposed by Sweden and the European Commission later joined the project as 8 a co-lead. In 2019, the OECD Secretariat was added to coordinate input from expert 9 consultants. The initial objectives of the project were to: 10 draft a review of the biology of retinoid signalling pathway, 11 describe retinoid-mediated effects on various organ systems, 12 identify relevant retinoid in vitro and ex vivo assays that measure mechanistic 13 effects of chemicals for development, and 14 Identify in vivo endpoints that could be added to existing test guidelines to 15 identify chemical effects on retinoid pathway signalling. 16 2. This DRP is intended to expand the recommendations for the retinoid pathway 17 included in the OECD Detailed Review Paper on the State of the Science on Novel In 18 vitro and In vivo Screening and Testing Methods and Endpoints for Evaluating 19 Endocrine Disruptors (DRP No 178). The retinoid signalling pathway was one of seven 20 endocrine pathways considered to be susceptible to environmental endocrine disruption 21 and for which relevant endpoints could be measured in new or existing OECD Test 22 Guidelines for evaluating endocrine disruption. Due to the complexity of retinoid 23 signalling across multiple organ systems, this effort was foreseen as a multi-step process.
    [Show full text]
  • Table 2. Significant
    Table 2. Significant (Q < 0.05 and |d | > 0.5) transcripts from the meta-analysis Gene Chr Mb Gene Name Affy ProbeSet cDNA_IDs d HAP/LAP d HAP/LAP d d IS Average d Ztest P values Q-value Symbol ID (study #5) 1 2 STS B2m 2 122 beta-2 microglobulin 1452428_a_at AI848245 1.75334941 4 3.2 4 3.2316485 1.07398E-09 5.69E-08 Man2b1 8 84.4 mannosidase 2, alpha B1 1416340_a_at H4049B01 3.75722111 3.87309653 2.1 1.6 2.84852656 5.32443E-07 1.58E-05 1110032A03Rik 9 50.9 RIKEN cDNA 1110032A03 gene 1417211_a_at H4035E05 4 1.66015788 4 1.7 2.82772795 2.94266E-05 0.000527 NA 9 48.5 --- 1456111_at 3.43701477 1.85785922 4 2 2.8237185 9.97969E-08 3.48E-06 Scn4b 9 45.3 Sodium channel, type IV, beta 1434008_at AI844796 3.79536664 1.63774235 3.3 2.3 2.75319499 1.48057E-08 6.21E-07 polypeptide Gadd45gip1 8 84.1 RIKEN cDNA 2310040G17 gene 1417619_at 4 3.38875643 1.4 2 2.69163229 8.84279E-06 0.0001904 BC056474 15 12.1 Mus musculus cDNA clone 1424117_at H3030A06 3.95752801 2.42838452 1.9 2.2 2.62132809 1.3344E-08 5.66E-07 MGC:67360 IMAGE:6823629, complete cds NA 4 153 guanine nucleotide binding protein, 1454696_at -3.46081884 -4 -1.3 -1.6 -2.6026947 8.58458E-05 0.0012617 beta 1 Gnb1 4 153 guanine nucleotide binding protein, 1417432_a_at H3094D02 -3.13334396 -4 -1.6 -1.7 -2.5946297 1.04542E-05 0.0002202 beta 1 Gadd45gip1 8 84.1 RAD23a homolog (S.
    [Show full text]
  • Watsonjn2018.Pdf (1.780Mb)
    UNIVERSITY OF CENTRAL OKLAHOMA Edmond, Oklahoma Department of Biology Investigating Differential Gene Expression in vivo of Cardiac Birth Defects in an Avian Model of Maternal Phenylketonuria A THESIS SUBMITTED TO THE GRADUATE FACULTY In partial fulfillment of the requirements For the degree of MASTER OF SCIENCE IN BIOLOGY By Jamie N. Watson Edmond, OK June 5, 2018 J. Watson/Dr. Nikki Seagraves ii J. Watson/Dr. Nikki Seagraves Acknowledgements It is difficult to articulate the amount of gratitude I have for the support and encouragement I have received throughout my master’s thesis. Many people have added value and support to my life during this time. I am thankful for the education, experience, and friendships I have gained at the University of Central Oklahoma. First, I would like to thank Dr. Nikki Seagraves for her mentorship and friendship. I lucked out when I met her. I have enjoyed working on this project and I am very thankful for her support. I would like thank Thomas Crane for his support and patience throughout my master’s degree. I would like to thank Dr. Shannon Conley for her continued mentorship and support. I would like to thank Liz Bullen and Dr. Eric Howard for their training and help on this project. I would like to thank Kristy Meyer for her friendship and help throughout graduate school. I would like to thank my committee members Dr. Robert Brennan and Dr. Lilian Chooback for their advisement on this project. Also, I would like to thank the biology faculty and staff. I would like to thank the Seagraves lab members: Jailene Canales, Kayley Pate, Mckayla Muse, Grace Thetford, Kody Harvey, Jordan Guffey, and Kayle Patatanian for their hard work and support.
    [Show full text]
  • Supplementary Figure S4
    18DCIS 18IDC Supplementary FigureS4 22DCIS 22IDC C D B A E (0.77) (0.78) 16DCIS 14DCIS 28DCIS 16IDC 28IDC (0.43) (0.49) 0 ADAMTS12 (p.E1469K) 14IDC ERBB2, LASP1,CDK12( CCNE1 ( NUTM2B SDHC,FCGR2B,PBX1,TPR( CD1D, B4GALT3, BCL9, FLG,NUP21OL,TPM3,TDRD10,RIT1,LMNA,PRCC,NTRK1 0 ADAMTS16 (p.E67K) (0.67) (0.89) (0.54) 0 ARHGEF38 (p.P179Hfs*29) 0 ATG9B (p.P823S) (0.68) (1.0) ARID5B, CCDC6 CCNE1, TSHZ3,CEP89 CREB3L2,TRIM24 BRAF, EGFR (7p11); 0 ABRACL (p.R35H) 0 CATSPER1 (p.P152H) 0 ADAMTS18 (p.Y799C) 19q12 0 CCDC88C (p.X1371_splice) (0) 0 ADRA1A (p.P327L) (10q22.3) 0 CCNF (p.D637N) −4 −2 −4 −2 0 AKAP4 (p.G454A) 0 CDYL (p.Y353Lfs*5) −4 −2 Log2 Ratio Log2 Ratio −4 −2 Log2 Ratio Log2 Ratio 0 2 4 0 2 4 0 ARID2 (p.R1068H) 0 COL27A1 (p.G646E) 0 2 4 0 2 4 2 EDRF1 (p.E521K) 0 ARPP21 (p.P791L) ) 0 DDX11 (p.E78K) 2 GPR101, p.A174V 0 ARPP21 (p.P791T) 0 DMGDH (p.W606C) 5 ANP32B, p.G237S 16IDC (Ploidy:2.01) 16DCIS (Ploidy:2.02) 14IDC (Ploidy:2.01) 14DCIS (Ploidy:2.9) -3 -2 -1 -3 -2 -1 -3 -2 -1 -3 -2 -1 -3 -2 -1 -3 -2 -1 Log Ratio Log Ratio Log Ratio Log Ratio 12DCIS 0 ASPM (p.S222T) Log Ratio Log Ratio 0 FMN2 (p.G941A) 20 1 2 3 2 0 1 2 3 2 ERBB3 (p.D297Y) 2 0 1 2 3 20 1 2 3 0 ATRX (p.L1276I) 20 1 2 3 2 0 1 2 3 0 GALNT18 (p.F92L) 2 MAPK4, p.H147Y 0 GALNTL6 (p.E236K) 5 C11orf1, p.Y53C (10q21.2); 0 ATRX (p.R1401W) PIK3CA, p.H1047R 28IDC (Ploidy:2.0) 28DCIS (Ploidy:2.0) 22IDC (Ploidy:3.7) 22DCIS (Ploidy:4.1) 18IDC (Ploidy:3.9) 18DCIS (Ploidy:2.3) 17q12 0 HCFC1 (p.S2025C) 2 LCMT1 (p.S34A) 0 ATXN7L2 (p.X453_splice) SPEN, p.P677Lfs*13 CBFB 1 2 3 4 5 6 7 8 9 10 11
    [Show full text]
  • The Regulation of Lunatic Fringe During Somitogenesis
    THE REGULATION OF LUNATIC FRINGE DURING SOMITOGENESIS DISSERTATION Presented in Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy in the Graduate School of The Ohio State University By Emily T. Shifley ***** The Ohio State University 2009 Dissertation Committee: Approved by Professor Susan Cole, Advisor Professor Christine Beattie _________________________________ Professor Mark Seeger Advisor Graduate Program in Molecular Genetics Professor Michael Weinstein ABSTRACT Somitogenesis is the morphological hallmark of vertebrate segmentation. Somites bud from the presomitic mesoderm (PSM) in a sequential, periodic fashion and give rise to the rib cage, vertebrae, and dermis and muscles of the back. The regulation of somitogenesis is complex. In the posterior region of the PSM, a segmentation clock operates to organize cohorts of cells into presomites, while in the anterior region of the PSM the presomites are patterned into rostral and caudal compartments (R/C patterning). Both of these stages of somitogenesis are controlled, at least in part, by the Notch pathway and Lunatic fringe (Lfng), a glycosyltransferase that modifies the Notch receptor. To dissect the roles played by Lfng during somitogenesis, we created a novel allele that lacks cyclic Lfng expression within the segmentation clock, but that maintains expression during R/C somite patterning (Lfng∆FCE1). Lfng∆FCE1/∆FCE1 mice have severe defects in their anterior vertebrae and rib cages, but relatively normal sacral and tail vertebrae, unlike Lfng knockouts. Segmentation clock function is differentially affected by the ∆FCE1 deletion; during anterior somitogenesis the expression patterns of many clock genes are disrupted, while during posterior somitogenesis, certain clock components have recovered. R/C patterning occurs relatively normally in Lfng∆FCE1/∆FCE1 embryos, likely contributing to the partial phenotype rescue, and confirming that Lfng ii plays separate roles in the two regions of the PSM.
    [Show full text]
  • Modeling the Human Segmentation Clock with Pluripotent Stem Cells 2 3 Mitsuhiro Matsuda1,10, Yoshihiro Yamanaka2,10, Maya Uemura2,3, Mitsujiro Osawa4, 4 Megumu K
    bioRxiv preprint doi: https://doi.org/10.1101/562447; this version posted February 27, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 1 Modeling the Human Segmentation Clock with Pluripotent Stem Cells 2 3 Mitsuhiro Matsuda1,10, Yoshihiro Yamanaka2,10, Maya Uemura2,3, Mitsujiro Osawa4, 4 Megumu K. Saito4, Ayako Nagahashi4, Megumi Nishio3, Long Guo5, Shiro Ikegawa5, 5 Satoko Sakurai6, Shunsuke Kihara7, Michiko Nakamura6, Tomoko Matsumoto6, Hiroyuki 6 Yoshitomi2,3, Makoto Ikeya6, Takuya Yamamoto6,8, Knut Woltjen6,9, Miki Ebisuya1*, 7 Junya Toguchida2,3, Cantas Alev2* 8 9 1 Laboratory for Reconstitutive Developmental Biology, RIKEN Center for Biosystems 10 Dynamics Research (RIKEN BDR), Kobe 650-0047, Japan. 11 2 Department of Cell Growth and Differentiation, Center for iPS Cell Research and 12 Application (CiRA), Kyoto University, Kyoto 606-8507, Japan. 13 3 Department of Regeneration Science and Engineering, Institute for Frontier Life and 14 Medical Sciences, Kyoto University, Kyoto 606-8507, Japan. 15 4 Department of Clinical Application, Center for iPS Cell Research and Application 16 (CiRA), Kyoto University, Kyoto 606-8507, Japan. 17 5 Laboratory for Bone and Joint Diseases, RIKEN Center for Integrative Medical 18 Sciences (RIKEN IMS), Tokyo 108-8639, Japan. 19 6 Department of Life Science Frontiers, Center for iPS Cell Research and Application 20 (CiRA), Kyoto University, 606-8507, Kyoto 108-8639, Japan. 21 7 Department of Fundamental Cell Technology, Center for iPS Cell Research and 22 Application (CiRA), Kyoto University, Kyoto 606-8507, Japan. 23 8 AMED-CREST, AMED 1-7-1 Otemachi, Chiyodaku, Tokyo 100-004, Japan.
    [Show full text]
  • SUPPLEMENTARY DATA Supplementary Table 1. Top Ten
    SUPPLEMENTARY DATA Supplementary Table 1. Top ten most highly expressed protein-coding genes in the EndoC-βH1 cell line. Expression levels provided for non-mitochondrial genes in EndoC-βH1 and the corresponding expression levels in sorted primary human β-cells (1). Ensembl gene ID Gene Name EndoC-βH1 [RPKM] Primary β cells [RPKM] ENSG00000254647.2 INS 8012.452 166347.111 ENSG00000087086.9 FTL 3090.7454 2066.464 ENSG00000100604.8 CHGA 2853.107 1113.162 ENSG00000099194.5 SCD 1411.631 238.714 ENSG00000118271.5 TTR 1312.8928 1488.996 ENSG00000184009.5 ACTG1 1108.0277 839.681 ENSG00000124172.5 ATP5E 863.42334 254.779 ENSG00000156508.13 EEF1A1 831.17316 637.281 ENSG00000112972.10 HMGCS1 719.7504 22.104 ENSG00000167552.9 TUBA1A 689.1415 511.699 ©2016 American Diabetes Association. Published online at http://diabetes.diabetesjournals.org/lookup/suppl/doi:10.2337/db16-0361/-/DC1 SUPPLEMENTARY DATA Supplementary Table 2. List of genes selected for inclusion in the primary screen. Expression levels in EndoC-βH1 and sorted primary human β-cells are shown for all genes targeted for silencing in the primary screen, ordered by locus association (1). For gene selection, the following criteria were applied: we first considered (1) all protein-coding genes within 1 Mb of a type 2 diabetes association signal that (2) had non-zero expression (RPKM > 0) in both EndoC-βH1 and primary human β-cells. Previous studies have shown cis-eQTLs to form a relatively tight, symmetrical distribution around the target-gene transcription start site, and a 1 Mb cut-off is thus likely to capture most effector transcripts subject to cis regulation (2-5).
    [Show full text]
  • Supplementary Data Genbank Or OSE Vs RO NIA Accession Gene Name Symbol FC B-Value H3073C09 11.38 5.62 H3126B09 9.64 6.44 H3073B0
    Supplementary Data GenBank or OSE vs RO NIA accession Gene name Symbol FC B-value H3073C09 11.38 5.62 H3126B09 9.64 6.44 H3073B08 9.62 5.59 AU022767 Exportin 4 Xpo4 9.62 6.64 H3073B09 9.59 6.48 BG063925 Metallothionein 2 Mt2 9.23 18.89 H3064B07 9.21 6.10 H3073D08 8.28 6.10 AU021923 Jagged 1 Jag1 7.89 5.93 H3070D08 7.54 4.58 BG085110 Cysteine-rich protein 1 (intestinal) Crip1 6.23 16.40 BG063004 Lectin, galactose binding, soluble 1 Lgals1 5.95 10.36 BG069712 5.92 2.34 BG076976 Transcribed locus, strongly similar to NP_032521.1 lectin, galactose binding, soluble 1 5.64 8.36 BG062930 DNA segment, Chr 11, Wayne State University 99, expressed D11Wsu99e 5.63 8.76 BG086474 Insulin-like growth factor binding protein 5 Igfbp5 5.50 15.95 H3002d11 5.13 20.77 BG064706 Keratin complex 1, acidic, gene 19 Krt1-19 5.06 9.07 H3007A09 5.05 2.46 H3065F02 4.84 5.43 BG081752 4.81 1.25 H3010E09 4.71 11.90 H3064c11 4.43 1.00 BG069711 Transmembrane 4 superfamily member 9 Tm4sf9 4.29 1.23 BG077072 Actin, beta, cytoplasmic Actb 4.29 3.01 BG079788 Hemoglobin alpha, adult chain 1 Hba-a1 4.26 6.63 BG076798 4.23 0.80 BG074344 Mesothelin Msln 4.22 6.97 C78835 Actin, beta, cytoplasmic Actb 4.16 3.02 BG067531 4.15 1.61 BG073468 Hemoglobin alpha, adult chain 1 Hba-a1 4.10 6.23 H3154H07 4.08 5.38 AW550167 3.95 5.66 H3121B01 3.94 5.94 H3124f12 3.94 5.64 BG073608 Hemoglobin alpha, adult chain 1 Hba-a1 3.84 5.32 BG073617 Hemoglobin alpha, adult chain 1 Hba-a1 3.84 5.75 BG072574 Hemoglobin alpha, adult chain 1 Hba-a1 3.82 5.93 BG072211 Tumor necrosis factor receptor superfamily,
    [Show full text]
  • Heartbreak Hotel: a Convergence in Cardiac Regeneration Michael D
    © 2016. Published by The Company of Biologists Ltd | Development (2016) 143, 1435-1441 doi:10.1242/dev.133652 MEETING REVIEW Heartbreak hotel: a convergence in cardiac regeneration Michael D. Schneider* ABSTRACT along with Tbx6, binds an essential early mesodermal enhancer In February 2016, The Company of Biologists hosted an intimate shared by Mesp1 and Mesp2, and deletion of this element prevents gathering of leading international researchers at the forefront of Mesp1/2 activation, the epithelial-mesenchymal transition, and experimental cardiovascular regeneration, with its emphasis on induction of the cardiovascular progenitors. ‘Transdifferentiation and Tissue Plasticity in Cardiovascular Cardiovascular origins were also discussed by Christian Rejuvenation’. As I review here, participants at the workshop Mosimann (University of Zurich, Switzerland). In vertebrates revealed how understanding cardiac growth and lineage decisions such as zebrafish, lateral plate mesoderm (LPM)-derived cell at their most fundamental level has transformed the strategies in hand types include not only the heart, but also blood vessels, blood, that presently energize the prospects for human heart repair. kidney and pectoral fins. Mosimann described how a 6.5 kb fragment of the zebrafish draculin (drl) upstream region initially KEY WORDS: Cardiomyocyte, Heart, Regenerative medicine, labels all LPM derivatives but becomes restricted just to Stem cells cardiovascular and hematopoietic lineages and, later still in the heart, just to first heart field (FHF) descendants (Mosimann et al., Introduction 2015). Further dissection of the drl locus revealed a pan-LPM The first organ to be fashioned during embryogenesis – the heart – is enhancer plus anterior and posterior LPM enhancers, while drl the organ that contributes most, worldwide, to death, disability and reporter zebrafish showed that regulators of cardiac septation control healthcare system costs (Roth et al., 2015).
    [Show full text]
  • Reprogramming of Lysosomal Gene Expression by Interleukin-4 and Stat6 Brignull Et Al
    Reprogramming of lysosomal gene expression by interleukin-4 and Stat6 Brignull et al. Brignull et al. BMC Genomics 2013, 14:853 http://www.biomedcentral.com/1471-2164/14/853 Brignull et al. BMC Genomics 2013, 14:853 http://www.biomedcentral.com/1471-2164/14/853 RESEARCH ARTICLE Open Access Reprogramming of lysosomal gene expression by interleukin-4 and Stat6 Louise M Brignull1†, Zsolt Czimmerer2†, Hafida Saidi1,3, Bence Daniel2, Izabel Villela4,5, Nathan W Bartlett6, Sebastian L Johnston6, Lisiane B Meira4, Laszlo Nagy2,7 and Axel Nohturfft1* Abstract Background: Lysosomes play important roles in multiple aspects of physiology, but the problem of how the transcription of lysosomal genes is coordinated remains incompletely understood. The goal of this study was to illuminate the physiological contexts in which lysosomal genes are coordinately regulated and to identify transcription factors involved in this control. Results: As transcription factors and their target genes are often co-regulated, we performed meta-analyses of array-based expression data to identify regulators whose mRNA profiles are highly correlated with those of a core set of lysosomal genes. Among the ~50 transcription factors that rank highest by this measure, 65% are involved in differentiation or development, and 22% have been implicated in interferon signaling. The most strongly correlated candidate was Stat6, a factor commonly activated by interleukin-4 (IL-4) or IL-13. Publicly available chromatin immunoprecipitation (ChIP) data from alternatively activated mouse macrophages show that lysosomal genes are overrepresented among Stat6-bound targets. Quantification of RNA from wild-type and Stat6-deficient cells indicates that Stat6 promotes the expression of over 100 lysosomal genes, including hydrolases, subunits of the vacuolar H+ ATPase and trafficking factors.
    [Show full text]
  • A Gene Regulation Network Controlled by Celf1 Protein– Rbpj Mrna Interaction in Xenopus Somite Segmentation
    1078 Research Article A gene regulation network controlled by Celf1 protein– rbpj mRNA interaction in Xenopus somite segmentation Marie Cibois1,2,3, Carole Gautier-Courteille1,2, Laurent Kodjabachian3 and Luc Paillard1,2,* 1Universite´ de Rennes 1, Universite´ Europe´enne de Bretagne, Biosit, CS 34317, 35043 Rennes Cedex, France 2CNRS UMR 6290 Institut de Ge´ne´tique et De´veloppement de Rennes, CS 34317, 35043 Rennes Cedex, France 3Institut de Biologie du De´veloppement de Marseille, Aix-Marseille Universite´, CNRS UMR7288, Case 907, 13288 Marseille Cedex 09, France *Author for correspondence ([email protected]) Biology Open 2, 1078–1083 doi: 10.1242/bio.20135629 Received 30th May 2013 Accepted 18th July 2013 Summary Somite segmentation is impaired in Xenopus celf1 morphant FGF pathway antagonized RA signalling through expression of embryos. The Celf1 RNA-binding protein targets bound cyp26a, our results suggest that Rbpj mediates this antagonism. mRNAs for rapid degradation, and antisense approaches Furthermore, they show that the post-transcriptional demonstrated that segmentation defects in celf1 morphants repression exerted by Celf1 on rbpj mRNA is required to were due to a derepression of rbpj mRNA. Rbpj protein is a key keep cyp26a expression under the control of FGF signalling. player of Notch signalling. Because segmentation involves We conclude that rbpj repression by Celf1 is important to complex cross-talk between several signalling pathways, we couple the FGF and RA pathways in Xenopus segmentation. analysed how rbpj derepression impacted these pathways. We found that rbpj derepression stimulated the Notch pathway. ß 2013. Published by The Company of Biologists Ltd. This is an Notch positively controlled the expression of cyp26a, which Open Access article distributed under the terms of the Creative encodes a retinoic acid (RA)-degrading enzyme.
    [Show full text]