Beyond a Pedagogical Tool: 30 Years of Molecular Biology of the Cell
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Francis Crick in Molecular Biology
2019 Asia-Pacific Conference on Emerging Technologies and Engineering (ACETE 2019) Francis Crick in Molecular Biology Sun Yongping College of Physic and Electronic Information, Inner Mongolia Normal University, Hohhot, China Keywords: Crick, DNA, Protein, Genetic Codes, Molecular Biology Abstract: This article is a tribute to Francis crick, a biophysicist who passed away on July 28, 2004. Francis crick, James Watson and Maurice Wilkins were jointly awarded the 1962 Nobel Prize for physiology or medicine for discovering the molecular structure of nucleic acids and its significance for information transfer in living material. It is pointed out that the diverse background and unique sensitivity of crick to science enabled him to have great insights into frontier research. He had a special capacity for prudent and logical thinking, which contributed so much to the development of molecular biology. Based on Francis crick’s academic achievements in molecular biology and by virtue of internal history approaches such as concept analysis and literature research, this paper is aimed at revealing the historical contributions of crick in a condensed way and to commemorate his work. 1. Introduction Francis crick (figure 1) was born on June 8, 1916 as an English citizen, and he left the world, aged 88. With lifelong devotion to scientific research, crick is credited as one of the central figures in the molecular revolution that swept through biology in the latter half of the twentieth century [1]. Keen on seeking after and tackling the profound problems, he developed a passion for biology although crick did research in physics at the beginning of his scientific life [2,3]. -
Francis HC Crick
Francis H. C. Crick: memories of a friend of Francis and Odile The world feels strange without Francis. It is of course full of memories of him. Mostly memories of the charismatic personality, of the brilliant mind, of the great scientist, of the stories of his discoveries in molecular biology. After all, the names of Watson and Crick will be with us as long as Einstein’s and Planck’s. My fondest memories of Francis are of a different kind. I met him at about the time – in ‘76 – when Francis and Odile moved from Cambridge, England to the Salk Institute in La Jolla, California. At the Salk he became a theoretical neuroscientist, following his second passion. After the mystery of life, the mystery of the mind. I saw him at F.O. Schmitt ‘s Neuroscience Research Program meetings. I visited Francis and Odile during the summers in their house on Portugal Place in Cambridge, England, with its golden helix above the front door. I went with them and the Orgels in trips to the desert. I saw him debating about consciousness with various guests at my home. In ‘79, I worked for an intense month at the Salk Institute with him and the late David Marr, trying to understand the connection between the architecture of visual cortex and several intriguing aspects of our visual perception. In those years molecular biology was becoming the dominant science. I remember the difficulty – then, not now -- of getting neuroscience appointments through the well- earned intellectual arrogance of our friends and colleagues in the Department of Biology at MIT. -
Medical Advisory Board September 1, 2006–August 31, 2007
hoWard hughes medical iNstitute 2007 annual report What’s Next h o W ard hughes medical i 4000 oNes Bridge road chevy chase, marylaNd 20815-6789 www.hhmi.org N stitute 2007 a nn ual report What’s Next Letter from the president 2 The primary purpose and objective of the conversation: wiLLiam r. Lummis 6 Howard Hughes Medical Institute shall be the promotion of human knowledge within the CREDITS thiNkiNg field of the basic sciences (principally the field of like medical research and education) and the a scieNtist 8 effective application thereof for the benefit of mankind. Page 1 Page 25 Page 43 Page 50 seeiNg Illustration by Riccardo Vecchio Südhof: Paul Fetters; Fuchs: Janelia Farm lab: © Photography Neurotoxin (Brunger & Chapman): Page 3 Matthew Septimus; SCNT images: by Brad Feinknopf; First level of Rongsheng Jin and Axel Brunger; iN Bruce Weller Blake Porch and Chris Vargas/HHMI lab building: © Photography by Shadlen: Paul Fetters; Mouse Page 6 Page 26 Brad Feinknopf (Tsai): Li-Huei Tsai; Zoghbi: Agapito NeW Illustration by Riccardo Vecchio Arabidopsis: Laboratory of Joanne Page 44 Sanchez/Baylor College 14 Page 8 Chory; Chory: Courtesy of Salk Janelia Farm guest housing: © Jeff Page 51 Ways Illustration by Riccardo Vecchio Institute Goldberg/Esto; Dudman: Matthew Szostak: Mark Wilson; Evans: Fred Page 10 Page 27 Septimus; Lee: Oliver Wien; Greaves/PR Newswire, © HHMI; Mello: Erika Larsen; Hannon: Zack Rosenthal: Paul Fetters; Students: Leonardo: Paul Fetters; Riddiford: Steitz: Harold Shapiro; Lefkowitz: capacity Seckler/AP, © HHMI; Lowe: Zack Paul Fetters; Map: Reprinted by Paul Fetters; Truman: Paul Fetters Stewart Waller/PR Newswire, Seckler/AP, © HHMI permission from Macmillan Page 46 © HHMI for Page 12 Publishers, Ltd.: Nature vol. -
Mapping Our Genes—Genome Projects: How Big? How Fast?
Mapping Our Genes—Genome Projects: How Big? How Fast? April 1988 NTIS order #PB88-212402 Recommended Citation: U.S. Congress, Office of Technology Assessment, Mapping Our Genes-The Genmne Projects.’ How Big, How Fast? OTA-BA-373 (Washington, DC: U.S. Government Printing Office, April 1988). Library of Congress Catalog Card Number 87-619898 For sale by the Superintendent of Documents U.S. Government Printing Office, Washington, DC 20402-9325 (order form can be found in the back of this report) Foreword For the past 2 years, scientific and technical journals in biology and medicine have extensively covered a debate about whether and how to determine the function and order of human genes on human chromosomes and when to determine the sequence of molecular building blocks that comprise DNA in those chromosomes. In 1987, these issues rose to become part of the public agenda. The debate involves science, technol- ogy, and politics. Congress is responsible for ‘(writing the rules” of what various Federal agencies do and for funding their work. This report surveys the points made so far in the debate, focusing on those that most directly influence the policy options facing the U.S. Congress, The House Committee on Energy and Commerce requested that OTA undertake the project. The House Committee on Science, Space, and Technology, the Senate Com- mittee on Labor and Human Resources, and the Senate Committee on Energy and Natu- ral Resources also asked OTA to address specific points of concern to them. Congres- sional interest focused on several issues: ● how to assess the rationales for conducting human genome projects, ● how to fund human genome projects (at what level and through which mech- anisms), ● how to coordinate the scientific and technical programs of the several Federal agencies and private interests already supporting various genome projects, and ● how to strike a balance regarding the impact of genome projects on international scientific cooperation and international economic competition in biotechnology. -
The Gene Wars: Science, Politics, and the Human Genome
8 Early Skirmishes | N A COMMENTARY introducing the March 7, 1986, issue of Science, I. Renato Dulbecco, a Nobel laureate and president of the Salk Institute, made the startling assertion that progress in the War on Cancer would be speedier if geneticists were to sequence the human genome.1 For most biologists, Dulbecco's Science article was their first encounter with the idea of sequencing the human genome, and it provoked discussions in the laboratories of universities and research centers throughout the world. Dul- becco was not known as a crusader or self-promoter—quite the opposite— and so his proposal attained credence it would have lacked coming from a less esteemed source. Like Sinsheimer, Dulbecco came to the idea from a penchant for thinking big. His first public airing of the idea came at a gala Kennedy Center event, a meeting organized by the Italian embassy in Washington, D.C., on Columbus Day, 1985.2 The meeting included a section on U.S.-Italian cooperation in science, and Dulbecco was invited to give a presentation as one of the most eminent Italian biologists, familiar with science in both the United States and Italy. He was preparing a review paper on the genetic approach to cancer, and he decided that the occasion called for grand ideas. In thinking through the recent past and future directions of cancer research, he decided it could be greatly enriched by a single bold stroke—sequencing the human genome. This Washington meeting marked the beginning of the Italian genome program.3 Dulbecco later made the sequencing -
Regional Oral History Office University of California the Bancroft Library Berkeley, California
Regional Oral History Office University of California The Bancroft Library Berkeley, California Daniel Koshland, Jr. Retrospective Oral History Project: Bruce Alberts Interviews conducted by Sally Smith Hughes in 2012 Copyright © 2014 by The Regents of the University of California ii Since 1954 the Regional Oral History Office has been interviewing leading participants in or well-placed witnesses to major events in the development of Northern California, the West, and the nation. Oral History is a method of collecting historical information through tape-recorded interviews between a narrator with firsthand knowledge of historically significant events and a well-informed interviewer, with the goal of preserving substantive additions to the historical record. The tape recording is transcribed, lightly edited for continuity and clarity, and reviewed by the interviewee. The corrected manuscript is bound with photographs and illustrative materials and placed in The Bancroft Library at the University of California, Berkeley, and in other research collections for scholarly use. Because it is primary material, oral history is not intended to present the final, verified, or complete narrative of events. It is a spoken account, offered by the interviewee in response to questioning, and as such it is reflective, partisan, deeply involved, and irreplaceable. ********************************* All uses of this manuscript are covered by a legal agreement between The Regents of the University of California and Bruce Alberts on March 21, 2014. The manuscript is thereby made available for research purposes. All literary rights in the manuscript, including the right to publish, are reserved to The Bancroft Library of the University of California, Berkeley. Excerpts up to 1000 words from this interview may be quoted for publication without seeking permission as long as the use is non-commercial and properly cited. -
Schedule of C Ourses
2020–2021 Schedule of Courses Schedule The David Rockefeller Graduate Program offers a multiple sclerosis); perception, cognition, and memory (autism, schizophrenia, and Alzheimer’s disease); consciousness (coma selection of courses, many of which students can and persistent vegetative state); mood (depression and anxiety); choose based on their interests and area of thesis motivation (addiction); sensation (pain); motor control (Parkinson’s research. Organized by Rockefeller faculty, and taught disease and ataxia); and trauma (brain or spinal cord injury and stroke). by scientists at the top of their fields, both from within Class length and frequency: Two-hour session, once weekly and outside of the university, these courses provide a Method of evaluation: Attendance, participation in the discussions, stimulating and dynamic curriculum that students can student presentations, and a final speculative paper relating a tailor to fit their personal goals, in consultation with disordered trait to a specific brain circuit the dean of graduate studies. Cell Biology SANFORD M. SIMON and SHAI SHAHAM Biochemical and Biophysical Methods, I & II This advanced course covering major topics in modern cell biology is GREGORY M. ALUSHIN, SETH A. DARST, SHIXIN LIU, and MICHAEL P. ROUT taught by faculty and visitors who are specialists in various disciplines. This course presents the fundamental principles of biochemistry Class length and frequency: Three-hour lecture, once weekly; and biophysics, with an emphasis on methodologies. In addition, two-hour discussion, twice weekly case studies are discussed, examining how physical and chemical methods have been used to establish the molecular mechanisms Prerequisite(s): Good knowledge of textbook cell biology of fundamental biological processes. -
Masthead (PDF)
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA Officers BRUCE ALBERTS, President of the JACK HALPERN, Vice President Academy PETER H. RAVEN, Home Secretary F. SHERWOOD ROWLAND, Foreign Secretary RONALD L. GRAHAM, Treasurer Editor-in-Chief NICHOLAS R. COZZARELLI Editorial Board MAY R. BERENBAUM CHARLES FEFFERMAN PHIL W. MAJERUS CARLA J. SHATZ of the PETER J. BICKEL WALTER M. FITCH PHILIPPA MARRACK KAI L. SIMONS Proceedings MARIO R. CAPECCHI JOSEPH L. GOLDSTEIN RICHARD D. MCKELVEY CHRISTOPHER A. SIMS WILLIAM CATTERALL CAROL A. GROSS ARNO G. MOTULSKY SOLOMON H. SNYDER ANTHONY CERAMI JACK HALPERN RONALD L. PHILLIPS CHRISTOPHER R. SOMERVILLE PIERRE CHAMBON BERTIL HILLE THOMAS D. POLLARD LARRY R. SQUIRE MARSHALL H. COHEN PIERRE C. HOHENBERG STANLEY B. PRUSINER STEVEN M. STANLEY STANLEY N. COHEN H. ROBERT HORVITZ CHARLES RADDING CHARLES F. STEVENS DAVID R. DAVIES ERICH P. IPPEN GIAN-CARLO ROTA FRANK H. STILLINGER HERMAN N. EISEN ALFRED G. KNUDSON JEREMY A. SABLOFF KARL K. TUREKIAN RAYMOND L. ERIKSON ROGER KORNBERG PAUL R. SCHIMMEL DON C. WILEY ANTHONY S. FAUCI ROBERT LANGER STUART L. SCHREIBER PETER G. WOLYNES NINA FEDOROFF HARVEY F. LODISH AARON J. SHATKIN Publisher: KENNETH R. FULTON Managing Editor: DIANE M. SULLENBERGER Associate Editorial Manager: JOHN M. MALLOY Associate Manager for Production: JOANNE D’AMICO Production Coordinator: BARBARA A. BACON Editorial Coordinators: AZADEH FULLMER,DANIEL H. SALSBURY Editorial Assistants: RENITA M. JOHNSON,BARBARA J. ORTON,JOE N. HARPE,DORIS DIASE System Administrator: MARILYN J. MASON Financial Manager: JOSEPH F. RZEPKA,JR. Financial Assistant: JULIA A. LITTLE PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (ISSN-0027-8424) is published biweekly by THE NATIONAL ACADEMY OF SCIENCES. -
Francis Crick Personal Papers
http://oac.cdlib.org/findaid/ark:/13030/kt1k40250c No online items Francis Crick Personal Papers Special Collections & Archives, UC San Diego Special Collections & Archives, UC San Diego Copyright 2007, 2016 9500 Gilman Drive La Jolla 92093-0175 [email protected] URL: http://libraries.ucsd.edu/collections/sca/index.html Francis Crick Personal Papers MSS 0660 1 Descriptive Summary Languages: English Contributing Institution: Special Collections & Archives, UC San Diego 9500 Gilman Drive La Jolla 92093-0175 Title: Francis Crick Personal Papers Creator: Crick, Francis Identifier/Call Number: MSS 0660 Physical Description: 14.6 Linear feet(32 archives boxes, 4 card file boxes, 2 oversize folders, 4 map case folders, and digital files) Physical Description: 2.04 Gigabytes Date (inclusive): 1935-2007 Abstract: Personal papers of British scientist and Nobel Prize winner Francis Harry Compton Crick, who co-discovered the helical structure of DNA with James D. Watson. The papers document Crick's family, social and personal life from 1938 until his death in 2004, and include letters from friends and professional colleagues, family members and organizations. The papers also contain photographs of Crick and his circle; notebooks and numerous appointment books (1946-2004); writings of Crick and others; film and television projects; miscellaneous certificates and awards; materials relating to his wife, Odile Crick; and collected memorabilia. Scope and Content of Collection Personal papers of Francis Crick, the British molecular biologist, biophysicist, neuroscientist, and Nobel Prize winner who co-discovered the helical structure of DNA with James D. Watson. The papers provide a glimpse of his social life and relationships with family, friends and colleagues. -
18-19--425 Cambridge School of Art Brochure AHSS 2020.Indd
2019/20 Prospectus Inspiring creativity since 1858 aru.ac.uk/csa About Cambridge School of Art 2-19 Come and talk to us 20-21 Spotlight on…. 22-39 Undergraduate courses 40-73 Postgraduate courses 74-83 Get in touch 84 CLOSER TO CREATIVITY 2 A creative community like no other – 160 years of innovation, experimentation and collaboration Digital glitches, inky spills, happy We are proud of our past, but even more accidents and breakthrough moments excited about our future. As one of our – they’re all part of the creative process, students, you will have access to industry- and here at Cambridge School of Art we standard facilities, from traditional celebrate them all. printmaking and letterpress equipment, 3D workshops and making spaces, to A creative community like no other, we state of the art digital animation software, offer distinctive programmes that build on 3D printing and laser-cutting technology, our history of over 160 years of innovation, enabling you to learn expert skills as you experimentation and collaboration. Home explore your talents and discover new to students studying for undergraduate, ones that will prepare you for professional MA and doctoral qualifications across art, practice. design and visual communication, we are focused on developing the individual As well as bringing you closer to the creativity of each and every one of our creative and cultural industries through students through our innovative and live briefs, work placements and supportive studio-based courses. internships, we will provide you with the encouragement and practical support to Experimentation and risk-taking are key to showcase your creativity—whether you’re everything we do, allowing you to express incubating an early stage business idea in your imagination, develop your creativity our Start-Up Lab, pitching it to potential and find your own unique visual language, investors as part of the annual Big Pitch, as you produce a portfolio of work that or collaborating with local museums or will help you stand out in your future galleries to install your latest exhibition. -
Introducción a La Biología Molecular E Historia Del Adn
INTRODUCCIÓN A LA BIOLOGÍA MOLECULAR E HISTORIA DEL ADN Dr. Raúl N. Ondarza Profesor Titular de Bioquímica, Facultad de Medicina, UNAM e Investigador en Ciencias Médicas, Centro de Investigaciones Sobre Enfermedades Infecciosas, INSP ¿QUÉ ES LA BIOLOGIA MOLECULAR ? Según Crick es un término ambiguo que se emplea en dos formas: La primera en un sentido muy general que puede ser entender algún problema biológico a nivel molecular. La segunda forma es más clásica, se refiere a moléculas biológicas de elevado peso molecular; ej. Acidos nucleicos y proteínas. La simplicidad y la universalidad de los mecanismos básicos que operan en Biología, han permitido el avance espectacular de la Biología Molecular, sobre todo en el sentido clásico del término. LA BIOLOGÍA MOLECULAR TIENE SU ORIGEN EN TRES ESCUELAS a) La estructural y tridimensional de los británicos: Cristalografía por rayos X de la hemoglobina por Perutz, la mioglobina por Kendrew y la hélice alfa de las proteínas por Linus Pauling, Norteamericano . Max F. Perutz 1914 - 2002 John C. Kendrew 1917-1997 Linus C. Pauling 1901-1994 b) La genética unidimensional con el grupo de los fagos por: Max L. H. Delbruck, Alfred D. Hershey y Salvador Luria. 1906-1981 1908-1997 1912-1991 c) La Escuela Francesa de la Biología Molecular: Uso de la Genética Microbiana. ➢ Francoise Jacob, André Lwoff y Jacques L. Monod abordaron un problema diferente que fue un paso conceptual más allá de la expresión del gen, o sea la regulación y la interacción de los eventos que determinan el gen. EL DESCUBRIMIENTO CIENTÍFICO SE PUEDE CLASIFICAR EN TRES CATEGORÍAS Segun D. -
Nucleosomal Barriers Can Accelerate Cohesin Mediated Loop Formation in Chromatin
bioRxiv preprint doi: https://doi.org/10.1101/861161; this version posted December 22, 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. The accidental ally: Nucleosomal barriers can accelerate cohesin mediated loop formation in chromatin Ajoy Maji1, Ranjith Padinhateeri2, Mithun K. Mitra1,*, 1 Department of Physics, IIT Bombay, Mumbai 400076, India 2 Department of Biosciences and Bioengineering, IIT Bombay, Mumbai 400076, India * [email protected] Abstract An important question in the context of the 3D organization of chromosomes is the mechanism of formation of large loops between distant base pairs. Recent experiments suggest that the formation of loops might be mediated by Loop Extrusion Factor proteins like cohesin. Experiments on cohesin have shown that cohesins walk diffusively on the DNA, and that nucleosomes act as obstacles to the diffusion, lowering the permeability and hence reducing the effective diffusion constant. An estimation of the times required to form the loops of typical sizes seen in Hi-C experiments using these low effective diffusion constants leads to times that are unphysically large. The puzzle then is the following, how does a cohesin molecule diffusing on the DNA backbone achieve speeds necessary to form the large loops seen in experiments? We propose a simple answer to this puzzle, and show that while at low densities, nucleosomes act as barriers to cohesin diffusion, beyond a certain concentration, they can reduce loop formation times due to a subtle interplay between the nucleosome size and the mean linker length.