Supplemental Tables.Pdf

Total Page:16

File Type:pdf, Size:1020Kb

Supplemental Tables.Pdf Supplemental Table 1. Top transcription factors/regulators predicted to be responsible for the global gene expression changes caused by Gremlin1 knockdown. p-values IN528, IN528, 3691, 3691, shGrem1 shGrem1 shGrem1 shGrem1 Regulator Activation 485 2456 485 2456 Average CDKN1A Activated 4.75E-37 1.61E-37 2.56E-44 4.75E-37 2.78E-37 let-7 Activated 3.88E-21 2.43E-21 9.25E-20 3.88E-21 2.57E-20 RB1 Activated 1.17E-19 2.84E-21 1.86E-22 1.17E-19 5.93E-20 TP53 Activated 3.03E-19 2.63E-22 4.64E-28 3.03E-19 1.52E-19 VEGF Inhibited 2.57E-17 6.24E-18 1.22E-20 2.57E-17 1.44E-17 CCND1 Inhibited 3.23E-17 7.69E-19 1.18E-21 3.23E-17 1.63E-17 CDK4 Inhibited 4.64E-17 6.22E-19 3.56E-21 4.64E-17 2.34E-17 ERBB2 Inhibited 3.36E-16 6.67E-19 1.99E-21 3.36E-16 1.68E-16 NUPR1 Activated 1.07E-15 1.11E-15 3.44E-15 1.07E-15 1.67E-15 E2F1 Inhibited 2.67E-20 4.15E-18 9.62E-15 2.67E-20 2.41E-15 HGF Inhibited 6.50E-15 7.37E-19 1.29E-22 6.50E-15 3.25E-15 CDKN2A Activated 8.66E-15 1.90E-16 1.67E-19 8.66E-15 4.38E-15 E2F4 Inhibited 5.40E-34 4.40E-32 3.89E-13 5.40E-34 9.73E-14 FOXM1 Inhibited 1.12E-10 1.09E-10 1.17E-17 1.12E-10 8.33E-11 RBL1 Activated 7.15E-09 1.45E-10 3.88E-11 7.15E-09 3.62E-09 Supplemental Table 2. RT-PCR primers used in this study Gene Protein Directionality Sequence Actin Actin Forward 5’-ACCTTCTACAATGAGCTGCG-3’ Actin Actin Reverse 5’-CCTGGATAGCAACGTACATGG-3’ BMP2 BMP2 Forward 5’-CTACATGCTAGACCTGTATCGC-3’ BMP2 BMP2 Reverse 5’-CCCACTCGTTTCTGGTAGTTC-3’ BMP4 BMP4 Forward 5’-GCACTGGTCTTGAGTATCCTG-3’ BMP4 BMP4 Reverse 5’-TGCTGAGGTTAAAGAGGAAACG-3’ BMP7 BMP7 Forward 5’-CTGTATGTCAGCTTCCGAGAC-3’ BMP7 BMP7 Reverse 5’-CGTTCATGTAGGAGTTCAGAGG-3’ BMPR1A BMPR1a Forward 5’-CTGGGCCTTGCTGTTAAATTC-3’ BMPR1A BMPR1a Reverse 5’-GTAGGGCTGGAAGTGGTTTT-3’ BMPR1B BMPR1b Forward 5’-CTGCACAGAAAGGAACGAATG-3’ BMPR1B BMPR1b Reverse 5’-AGGACCAAGAGCAAACTACAG-3’ Chrd Chordin Forward 5’-TCCGCTTCTCTATCTCCTACAG-3’ Chrd Chordin Reverse 5’-GAGACAACCGAGGCACTG-3’ Chrdl1 Ventroptin Forward 5’-AGAAGTACAGAGTGGGTGAGAG-3’ Chrdl1 Ventroptin Reverse 5’-CACAGGAGAAAGGCAATGAAC-3’ GalC Galactosyl- Forward 5’-AATTATCAAGGTCTCCAGCGAG-3’ ceramidase GalC Galactosyl- Reverse 5’- CATCTTTTGCTGAATGGGTTCC-3’ ceramidase GAPDH GAPDH Forward 5’- GAAGGTGAAGGTCGGAGTC-3’ GAPDH GAPDH Reverse 5’- GAAGATGGTGATGGGATTTC-3’ GFAP GFAP Forward 5’-TGTGTGAGTAAGAAGGGACCGCAA-3’ GFAP GFAP Reverse 5’-GCAGGGCATGACTTGTCCCATTT-3’ Grem1 Gremlin1 Forward 5’-ATGAGCCGCACAGCCTACACG-3’ Grem1 Gremlin1 Reverse 5’-TTAATCCAAATCGATGGATATGC-3’ Map2 Map-2 Forward 5’- TGAGGTTGCCAGGAGGAAATCAGT-3’ Map2 Map-2 Reverse 5’- AGGTGATGGCAATGGGACTGTGTA-3’ Nog Noggin Forward 5’-CAGCACTATCTCCACATCCG-3’ Nog Noggin Reverse 5’-TCGTTCAGATCCTTTTCCTTGG-3’ Olig2 Olig2 Forward 5’-GGTAAGTGCGCAATGCTAAGCTGT-3’ Olig2 Olig2 Reverse 5’-TACAAAGCCCAGTTTGCAACGCAG-3’ S100b S100b Forward 5’-AGGGAGACAAGCACAAGCTGAAGA-3’ S100b S100b Reverse 5’-TGTCCACAACCTCCTGCTCTTTGA-3’ Sox2 Sox2 Forward 5’-CACACTGCCCCTCTCAC-3’ Sox2 Sox2 Reverse 5’-TCCATGCTGTTTCTTACTCTCC-3’ Tuj1 β3-tubulin Forward 5’- TCGTTGTCGATGCAGTAGGTCTCA-3’ Tuj1 β3-tubulin Reverse 5’- ATCAGCAAGGTGCGTGAGGAGTAT-3’ VWC2 Brorin Forward 5’-CCTGTGTACGAGCCTGATC-3’ VWC2 Brorin Reverse 5’-ATTCTCCATGTGCCTTCCTC-3’ Supplemental Table 3. Primers for TP53 amplification Exon Directionality Sequence Exon 4 Forward 5’-CCTGGTCCTCTGACTGCTCTTTTCACCCA-3’ Exon 4 Reverse 5’-GGCCAGGCATTGAAGTCTCAT-3’ Exon 5 Forward 5’-CAACTCTGTCTCCTTCCT-3’ Exon 5 Reverse 5’-TGTCGTCTCTCCAGCCCC-3’ Exon 6 Forward 5’-AGAGACGACAGGGCTGGTTG-3’ Exon 6 Reverse 5’-CTTAACCCCTCCTCCCAGAG-3’ Exon 7 Forward 5’-CCTCATCTTGGGCCTGTGTT-3’ Exon 7 Reverse 5’-AGTGTGCAGGGTGGCAAGTG-3’ Exon 8 Forward 5’-CCTTACTGCCTCTTGCTTCT-3’ Exon 8 Reverse 5’-ATAACTGCACCCTTGGTCTC-3’ Exon 9 Forward 5’-GGAGACCAAGGGTGCAGTTATGCCTCAG-3’ Exon 9 Reverse 5’-CCCAATTGCAGGTAAAACAG-3’ .
Recommended publications
  • BMP3 Suppresses Osteoblast Differentiation of Bone Marrow Stromal Cells Via Interaction with Acvr2b
    MUShare Faculty Publications and Research College of Osteopathic Medicine 1-1-2012 BMP3 Suppresses Osteoblast Differentiation of Bone Marrow Stromal Cells Via Interaction With Acvr2b. Shoichiro Kokabu Laura Gamer Karen Cox Jonathan W. Lowery Ph.D. Marian University - Indianapolis, [email protected] Kunikazu Tsuji See next page for additional authors Follow this and additional works at: https://mushare.marian.edu/com_fp Part of the Cells Commons, and the Genetics and Genomics Commons Recommended Citation Kokabu S, Gamer L, Cox K, Lowery JW, Kunikazu T, Econimedes A, Katagiri T, Rosen V. “BMP3 suppresses osteoblast differentiation of bone marrow stromal cells via interaction with Acvr2b.” Mol Endocrinol. 2012;26(1):87-94. PMC3248326. PMID: 22074949. This Article is brought to you for free and open access by the College of Osteopathic Medicine at MUShare. It has been accepted for inclusion in Faculty Publications and Research by an authorized administrator of MUShare. For more information, please contact [email protected]. Authors Shoichiro Kokabu, Laura Gamer, Karen Cox, Jonathan W. Lowery Ph.D., Kunikazu Tsuji, Regina Raz, Aris Economides, Takenobu Katagiri, and Vicki Rosen This article is available at MUShare: https://mushare.marian.edu/com_fp/12 ORIGINAL RESEARCH BMP3 Suppresses Osteoblast Differentiation of Bone Marrow Stromal Cells via Interaction with Acvr2b Shoichiro Kokabu, Laura Gamer, Karen Cox, Jonathan Lowery, Kunikazu Tsuji, Regina Raz, Aris Economides, Takenobu Katagiri, and Vicki Rosen Department of Developmental Biology (S.K., L.G., K.C., J.L., V.R.), Harvard School of Dental Medicine, Boston, Massachusetts 02115; Section of Orthopedic Surgery (K.T.),Tokyo Medical and Dental University, Tokyo 113-8510, Japan; Regeneron Pharmaceuticals (R.R., A.E.), Tarrytown, New York 10591; and Division of Pathophysiology (T.K.), Saitama Medical University, Saitama 359-8513, Japan Enhancing bone morphogenetic protein (BMP) signaling increases bone formation in a variety of settings that target bone repair.
    [Show full text]
  • Nodal Signaling Is Required for Mesodermal and Ventral but Not For
    © 2015. Published by The Company of Biologists Ltd | Biology Open (2015) 4, 830-842 doi:10.1242/bio.011809 RESEARCH ARTICLE Nodal signaling is required for mesodermal and ventral but not for dorsal fates in the indirect developing hemichordate, Ptychodera flava Eric Röttinger1,2,3,*, Timothy Q. DuBuc4, Aldine R. Amiel1,2,3 and Mark Q. Martindale4 ABSTRACT early fate maps of direct and indirect developing hemichordates, are Nodal signaling plays crucial roles in vertebrate developmental similar to those of indirect-developing echinoids (Colwin and processes such as endoderm and mesoderm formation, and axial Colwin, 1951; Cameron et al., 1987; Cameron et al., 1989; Cameron patterning events along the anteroposterior, dorsoventral and left- and Davidson, 1991; Henry et al., 2001). While the bilaterally right axes. In echinoderms, Nodal plays an essential role in the symmetric echinoderm larvae exhibit strong similarities to establishment of the dorsoventral axis and left-right asymmetry, but chordates in axial patterning and germ layer specification events, not in endoderm or mesoderm induction. In protostomes, Nodal adult body plan comparisons in echinoderms have been difficult due signaling appears to be involved only in establishing left-right to their unique adult pentaradial symmetry. However, both the larval asymmetry. Hence, it is hypothesized that Nodal signaling has and adult body plans of enteropneust hemichordates are bilaterally been co-opted to pattern the dorsoventral axis of deuterostomes and symmetric, and larvae from indirect developing hemichordates for endoderm, mesoderm formation as well as anteroposterior such as Ptychodera flava (P. flava) share similarities in patterning in chordates. Hemichordata, together with echinoderms, morphology, axial organization, and developmental fate map with represent the sister taxon to chordates.
    [Show full text]
  • Secreted Bone Morphogenetic Protein Antagonists of the Chordin Family
    Article in press - uncorrected proof BioMol Concepts, Vol. 1 (2010), pp. 297–304 • Copyright ᮊ by Walter de Gruyter • Berlin • New York. DOI 10.1515/BMC.2010.026 Review Secreted bone morphogenetic protein antagonists of the Chordin family Nobuyuki Itoha,* and Hiroya Ohtaa factor b (TGFb) superfamily. Originally identified in the Department of Genetic Biochemistry, Kyoto University protein extracts of deminerized bone, BMPs promote endo- Graduate School of Pharmaceutical Sciences, Sakyo, chondral bone formation. However, they also play diverse Kyoto 606-8501, Japan roles in developmental and metabolic processes at the embry- onic and postnatal stages. BMPs are secreted as dimers and * Corresponding author activate specific Ser/Thr kinase receptors at cell surfaces. e-mail: [email protected] The activated receptors propagate BMP signals via the phos- phorylation of Smad proteins and other non-canonical intra- Abstract cellular effectors (1, 2). The actions of BMPs are inhibited by several secreted Chordin, Chordin-like 1, and Chordin-like 2 are secreted BMP antagonists. Most extracellular BMP antagonists inhibit bone morphogenetic protein (BMP) antagonists with highly BMPs by binding to them. The amino acid sequences of conserved Chordin-like cysteine-rich domains. Recently, secreted BMP antagonists are characterized by cysteine-rich Brorin and Brorin-like have been identified as new Chordin- (CR) domains. On the basis of the spacing of cysteine resi- like BMP antagonists. A Chordin ortholog, Short gastrula- dues in the CR domains, secreted BMP antagonists can be tion, has been identified in Drosophila, a protostome, but not classified into five groups; the Dan family, Twisted gastru- other orthologs.
    [Show full text]
  • TGF Beta Signaling Pathway 1 TGF Beta Signaling Pathway
    TGF beta signaling pathway 1 TGF beta signaling pathway The Transforming growth factor beta (TGFβ) signaling pathway is involved in many cellular processes in both the adult organism and the developing embryo including cell growth, cell differentiation, apoptosis, cellular homeostasis and other cellular functions. In spite of the wide range of cellular processes that the TGFβ signaling pathway regulates, the process is relatively simple. TGFβ superfamily ligands bind to a type II receptor, which recruits and phosphorylates a type I receptor. The type I receptor then phosphorylates receptor-regulated SMADs (R-SMADs) which can now bind the coSMAD SMAD4. R-SMAD/coSMAD complexes accumulate in the nucleus where they act as transcription factors and participate in the regulation of target gene expression. Mechanism Ligand Binding The TGF Beta superfamily of ligands include: Bone morphogenetic proteins (BMPs), Growth and differentiation factors (GDFs), Anti-müllerian hormone (AMH), Activin, Nodal and TGFβ's[1] . Signalling begins with the binding of a TGF beta superfamily ligand to a TGF beta type II receptor. The type II receptor is a serine/threonine receptor kinase, which catalyses the phosphorylation of the Type I receptor. Each class of ligand binds to a specific type II receptor[2] .In mammals there are seven known type I receptors and five type II receptors[3] . There are three activins: Activin A, Activin B and Activin AB. Activins are involved in embryogenesis and osteogenesis. They also regulate many hormones including pituitary, gonadal and hypothalamic hormones as well as insulin. They are also nerve cell survival factors. The BMPs bind to the Bone morphogenetic protein receptor type-2 (BMPR2).
    [Show full text]
  • The Zinc Finger Gene Xblimp1 Controls Anterior Endomesodermal Cell Fate
    The EMBO Journal Vol.18 No.21 pp.6062–6072, 1999 The zinc finger gene Xblimp1 controls anterior endomesodermal cell fate in Spemann’s organizer Fla´ vio S.J.de Souza, Volker Gawantka, give rise to liver, foregut and prechordal endomesoderm Aitana Perea Go´ mez1, Hajo Delius2, (Pasteels, 1949; Nieuwkoop and Florschu¨tz, 1950; Keller, Siew-Lan Ang1 and Christof Niehrs3 1991; Bouwmeester et al., 1996). The activity of one gene expressed in the anterior endomesoderm, cerberus, has Division of Molecular Embryology and 2Division of Applied Tumour given strong molecular support to the idea that this region Virology, Deutsches Krebsforschungszentrum, Im Neuenheimer Feld is crucial in the process of head induction (reviewed in 280, D-69120 Heidelberg, Germany and 1Institut de Ge´ne´tique et de Biologie Moleculaire et Cellulaire, CNRS/INSERM/Universite´ Louis Slack and Tannahill, 1992; Gilbert and Saxen, 1993; Pasteur/Colle`ge de France, BP163, 67404 Illkirch cedex, Bouwmeester and Leyns, 1997; Niehrs, 1999). Cerberus CU de Strasbourg, France is a secreted factor able to induce ectopic heads including 3Corresponding author forebrain, eye, cement gland and heart in Xenopus (Bouwmeester et al., 1996). Independent evidence for the The anterior endomesoderm of the early Xenopus importance of endoderm in forebrain induction comes gastrula is a part of Spemann’s organizer and is from studies in mouse, where ablation of anterior visceral important for head induction. Here we describe endodermal cells (Thomas and Beddington, 1996) as well Xblimp1, which encodes a zinc finger transcriptional as inactivation of genes such as nodal (Varlet et al., 1997) repressor expressed in the anterior endomesoderm.
    [Show full text]
  • The Regulation of Mesodermal Progenitor Cell Commitment to Somitogenesis Subdivides the Zebrafish Body Musculature Into Distinct Domains
    Downloaded from genesdev.cshlp.org on September 24, 2021 - Published by Cold Spring Harbor Laboratory Press The regulation of mesodermal progenitor cell commitment to somitogenesis subdivides the zebrafish body musculature into distinct domains Daniel P. Szeto1 and David Kimelman2 Department of Biochemistry, University of Washington, Seattle, Washington 98195, USA The vertebrate musculature is produced from a visually uniform population of mesodermal progenitor cells (MPCs) that progressively bud off somites populating the trunk and tail. How the MPCs are regulated to continuously release cells into the presomitic mesoderm throughout somitogenesis is not understood. Using a genetic approach to study the MPCs, we show that a subset of MPCs are set aside very early in zebrafish development, and programmed to cell-autonomously enter the tail domain beginning with the 16th somite. Moreover, we show that the trunk is subdivided into two domains, and that entry into the anterior trunk, posterior trunk, and tail is regulated by interactions between the Nodal and bone morphogenetic protein (Bmp) pathways. Finally, we show that the tail MPCs are held in a state we previously called the Maturation Zone as they wait for the signal to begin entering somitogenesis. [Keywords: Bmp signaling; Nodal; T-box genes; MZoep; somite] Supplemental material is available at http://www.genesdev.org. Received March 29, 2006; revised version accepted May 12, 2006. The mesodermal progenitor cells (MPCs) are a popula- the presomitic mesoderm (Griffin and Kimelman 2002) tion of undifferentiated progenitor cells that originate in (this zone is not the same as the maturation front at the the early gastrula embryo (for review, see Schier et al.
    [Show full text]
  • How BMP Signaling Regulates Muscle Growth and Regeneration
    Journal of Developmental Biology Review Bu-M-P-ing Iron: How BMP Signaling Regulates Muscle Growth and Regeneration 1,2, 1,2, 1,2,3,4,5, Matthew J Borok y, Despoina Mademtzoglou y and Frederic Relaix * 1 Inserm, IMRB U955-E10, 94010 Créteil, France; [email protected] (M.J.B.); [email protected] (D.M.) 2 Faculté de santé, Université Paris Est, 94000 Creteil, France 3 Ecole Nationale Veterinaire d’Alfort, 94700 Maison Alfort, France 4 Etablissement Français du Sang, 94017 Créteil, France 5 APHP, Hopitaux Universitaires Henri Mondor, DHU Pepsy & Centre de Référence des Maladies Neuromusculaires GNMH, 94000 Créteil, France * Correspondence: [email protected]; Tel.: +33-149-813-940 These authors contributed equally to this work. y Received: 10 January 2020; Accepted: 7 February 2020; Published: 11 February 2020 Abstract: The bone morphogenetic protein (BMP) pathway is best known for its role in promoting bone formation, however it has been shown to play important roles in both development and regeneration of many different tissues. Recent work has shown that the BMP proteins have a number of functions in skeletal muscle, from embryonic to postnatal development. Furthermore, complementary studies have recently demonstrated that specific components of the pathway are required for efficient muscle regeneration. Keywords: development; regeneration; TGFβ; stem cells; satellite cells 1. Introduction As its name implies, the bone morphogenetic protein (BMP) signaling pathway was first identified as a key regulator of bone formation. Urist and colleagues isolated proteins from rabbit bone and then used them to induce bone formation in vitro or in vivo in the rat [1].
    [Show full text]
  • BMP Signaling Through ACVRI Is Required for Left–Right Patterning in the Early Mouse Embryo
    View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector Developmental Biology 276 (2004) 185–193 www.elsevier.com/locate/ydbio BMP signaling through ACVRI is required for left–right patterning in the early mouse embryo Satoshi Kishigamia,1, Shun-Ichi Yoshikawab,c, Trisha Castranioa, Kenji Okazakib, Yasuhide Furutac, Yuji Mishinaa,* aMolecular Developmental Biology Group, Laboratory of Reproductive and Developmental Toxicology, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, United States bDepartment of Molecular Biology, Biomolecular-Engineering Research Institute, Suita, Osaka 565-0874, Japan cUniversity of Texas, M.D. Anderson Cancer Center, Houston, TX 77030, United States Received for publication 14 September 2003, revised 7 July 2004, accepted 20 August 2004 Available online 18 September 2004 Abstract Vertebrate organisms are characterized by dorsal–ventral and left–right asymmetry. The process that establishes left–right asymmetry during vertebrate development involves bone morphogenetic protein (BMP)-dependent signaling, but the molecular details of this signaling pathway remain poorly defined. This study tests the role of the BMP type I receptor ACVRI in establishing left–right asymmetry in chimeric mouse embryos. Mouse embryonic stem (ES) cells with a homozygous deletion at Acvr1 were used to generate chimeric embryos. Chimeric embryos were rescued from the gastrulation defect of Acvr1 null embryos but exhibited abnormal heart looping and embryonic turning. High mutant contribution chimeras expressed left-side markers such as nodal bilaterally in the lateral plate mesoderm (LPM), indicating that loss of ACVRI signaling leads to left isomerism. Expression of lefty1 was absent in the midline of chimeric embryos, but shh, a midline marker, was expressed normally, suggesting that, despite formation of midline, its barrier function was abolished.
    [Show full text]
  • Bone Morphogenetic Protein-7 Is a MYC Target with Prosurvival Functions in Childhood Medulloblastoma
    Oncogene (2011) 30, 2823–2835 & 2011 Macmillan Publishers Limited All rights reserved 0950-9232/11 www.nature.com/onc ORIGINAL ARTICLE Bone morphogenetic protein-7 is a MYC target with prosurvival functions in childhood medulloblastoma G Fiaschetti1, D Castelletti1, S Zoller2, A Schramm3, C Schroeder4, M Nagaishi5, D Stearns6, M Mittelbronn7, A Eggert3, F Westermann4, H Ohgaki5, T Shalaby1, M Pruschy8, A Arcaro9 and MA Grotzer1 1Department of Oncology, University Children’s Hospital, Zurich, Switzerland; 2Functional Genomics Center Zurich, UZH/ETH, Zurich, Switzerland; 3Division of Hematology/Oncology, University Children’s Hospital Essen, Essen, Germany; 4Department Tumor Genetics, German Cancer Research Center (DKFZ), Heidelberg, Germany; 5Section of Molecular Pathology, International Agency for Research on Cancer, World Health Organization, Lyon, France; 6Department of Pathology, Johns Hopkins University, Baltimore, MD, USA; 7Institute of Neurology (Edinger Institute) Goethe-University Frankfurt, Frankfurt/Main, Germany; 8Department Radiation Oncology, University Hospital, Zurich, Switzerland and 9Division of Pediatric Hematology/Oncology, Department of Clinical Research, University of Bern, Bern, Switzerland Medulloblastoma (MB) is the most common malignant brain Introduction tumor in children. It is known that overexpression and/or amplification of the MYC oncogene is associated with poor Medulloblastoma (MB) represents >20% of all pedia- clinical outcome, but the molecular mechanisms and the tric tumors of the central nervous system (Gurney and MYC downstream effectors in MB remain still elusive. Kadan-Lottick, 2001), and is characterized by aggres- Besides contributing to elucidate how progression of MB sive clinical behavior and high risk of leptomeningeal takes place, most importantly, the identification of novel dissemination (Engelhard and Corsten, 2005). Multi- MYC-target genes will suggest novel candidates for targeted modal therapy (surgery, radiotherapy and chemother- therapy in MB.
    [Show full text]
  • Gremlin, Noggin, Chordin and Follistatin Differentially Modulate BMP Induced Suppression of Androgen Secretion by Bovine Ovarian Theca Cells
    Gremlin, noggin, chordin and follistatin differentially modulate BMP induced suppression of androgen secretion by bovine ovarian theca cells Article Accepted Version Glister, C., Regan, S. L., Samir, M. and Knight, P. G. (2019) Gremlin, noggin, chordin and follistatin differentially modulate BMP induced suppression of androgen secretion by bovine ovarian theca cells. Journal of Molecular Endocrinology, 62 (1). pp. 15-25. ISSN 0952-5041 doi: https://doi.org/10.1530/JME-18-0198 Available at http://centaur.reading.ac.uk/80330/ It is advisable to refer to the publisher’s version if you intend to cite from the work. See Guidance on citing . To link to this article DOI: http://dx.doi.org/10.1530/JME-18-0198 Publisher: Society for Endocrinology All outputs in CentAUR are protected by Intellectual Property Rights law, including copyright law. Copyright and IPR is retained by the creators or other copyright holders. Terms and conditions for use of this material are defined in the End User Agreement . www.reading.ac.uk/centaur CentAUR Central Archive at the University of Reading Reading’s research outputs online Page 1 of 29 Accepted Manuscript published as JME-18-0198.R1. Accepted for publication: 25-Oct-2018 1 Gremlin, Noggin, Chordin and follistatin differentially modulate BMP- 2 induced suppression of androgen secretion by bovine ovarian theca cells 3 4 Claire Glister1, Sheena L Regan2, Moafaq Samir1,3 and Phil G Knight1 5 1School of Biological Sciences, Hopkins Building, University of Reading, Whiteknights, Reading 6 RG6 6UB, UK 7 2School of Biomedical Sciences, Curtin University, Perth, WA 6845, Australia 8 3Current address: College of Veterinary Medicine, University of Wasit, Wasit, Iraq 9 10 11 corresponding author: [email protected] (PGK) 12 13 14 15 1 Copyright © 2018 Society for Endocrinology Downloaded from Bioscientifica.com at 11/02/2018 01:27:58PM via free access Accepted Manuscript published as JME-18-0198.R1.
    [Show full text]
  • Chordin Regulates Primitive Streak Development and the Stability of Induced Neural Cells, but Is Not Sufficient for Neural Induction in the Chick Embryo
    Development 125, 507-519 (1998) 507 Printed in Great Britain © The Company of Biologists Limited 1998 DEV4960 Chordin regulates primitive streak development and the stability of induced neural cells, but is not sufficient for neural induction in the chick embryo Andrea Streit1, Kevin J. Lee2, Ian Woo1, Catherine Roberts1,*, Thomas M. Jessell2 and Claudio D. Stern1,† 1Department of Genetics and Development, College of Physicians and Surgeons of Columbia University, 701 West 168th Street #1602, New York, NY 10032, USA 2Howard Hughes Medical Institute and Department of Biochemistry and Molecular Biophysics, College of Physicians and Surgeons of Columbia University, 701 West 168th Street, New York, NY 10032, USA *Present address: Molecular Medicine Unit, Institute of Child Health, 30, Guildford Street, London WC1N 1EH, UK †Author for correspondence (e-mail: [email protected]) Accepted 7 November 1997: published on WWW 13 January 1998 SUMMARY We have investigated the role of Bone Morphogenetic in regions outside the future neural plate does not induce Protein 4 (BMP-4) and a BMP antagonist, chordin, in the early neural markers L5, Sox-3 or Sox-2. Furthermore, primitive streak formation and neural induction in amniote neither BMP-4 nor BMP-7 interfere with neural induction embryos. We show that both BMP-4 and chordin are when misexpressed in the presumptive neural plate before expressed before primitive streak formation, and that or after primitive streak formation. However, chordin can BMP-4 expression is downregulated as the streak starts to stabilise the expression of early neural markers in cells that form. When BMP-4 is misexpressed in the posterior area have already received neural inducing signals.
    [Show full text]
  • Myostatin and the Control of Skeletal Muscle Mass Commentary Se-Jin Lee* and Alexandra C Mcpherron†
    gd9504.qxd 11/10/1999 12:12 PM Page 604 604 Myostatin and the control of skeletal muscle mass Commentary Se-Jin Lee* and Alexandra C McPherron† The mechanisms by which tissue size is controlled are poorly re-enter the cell cycle and continue to restore liver mass understood. Over 30 years ago, Bullough proposed the until the original liver size has been reached, at which existence of chalones, which act as tissue-specific negative point the hepatocytes stop proliferating [1]. How this growth regulators. The recent discovery of myostatin suggests process is controlled has been the subject of extensive that negative regulation of tissue growth may be an important study for many years. Perhaps the most fundamental ques- mechanism for controlling skeletal muscle mass and raises the tion that relates to the control of tissue size is how the possibility that growth inhibitors may also be involved in animal senses at any given time how much liver mass it regulating the size of other tissues. has. That is, immediately following the surgical procedure, how does the animal ‘know’ that it is missing a portion of Addresses its liver mass and that it is time to start the regeneration Department of Molecular Biology and Genetics, Johns Hopkins process? And how does the animal ‘know’ when its liver University School of Medicine, 725 North Wolfe Street, Baltimore, mass has been restored in order to stop this process? Maryland 21205, USA *e-mail: [email protected] †e-mail: [email protected] The chalone hypothesis A variety of hypotheses have been put forth in an attempt Current Opinion in Genetics & Development 1999, 9:604–607 to explain this phenomenon, many of which include a role Abbreviations for negative growth regulators [2].
    [Show full text]