Profile of Jay C. Dunlap

Total Page:16

File Type:pdf, Size:1020Kb

Profile of Jay C. Dunlap PROFILE PROFILE Profile of Jay C. Dunlap Paul Gabrielsen Science Writer On moonless nights, the wakes of oceangoing back to oceanography,” Dunlap says, “but I boats sparkle with the blue bioluminescence just thought clocks were the greatest things of unicellular dinoflagellates. As a graduate I’deverheardabout.” He chose to attend student at Harvard University, Jay C. Dunlap Harvard. pondered the carefully orchestrated biological Dunlap found Hastings’ approach to his rhythms that direct dinoflagellates to produce students’ research to be supportive but hands light only at night. Dunlap, a student of off. “He provided all these resources,” Dunlap oceanography at the time, realized that the says, “but he never told people what to do. He field of biological rhythms was still a wide- would give you great feedback on what you open frontier, with many fundamental ques- were doing, but you needed to find your own tions yet to be answered. “This was a place,” way. And if you were lucky enough to do that, he says, “where I could make a mark.” then you really learned how to do science.” Dunlap, Nathan Smith Professor and Chair In 1977, Dunlap attended a 10-week of Genetics at Dartmouth’s Geisel School of summer course on biological rhythms at Medicine and a member of the National Hopkins Marine Station in Pacific Grove, Academy of Sciences since 2009, has devoted California organized by Colin Pittendrigh, his career to answering those fundamental who, along with Hastings, had made pio- questions. His work has uncovered how cir- neering advances in the field of rhythms. The cadian rhythms work at a genetic level, how course attracted scientists studying rhythms environmental cues, such as light, can set bi- along with their graduate students, who, ological clocks, and how the clock can regu- Dunlap says, composed an entire generation Jay C. Dunlap in the 1990s with strains of late key cellular mechanisms. of rhythms biologists. Pittendrigh himself Neurospora and race tubes for visualizing circadian rhythm in development. Photo cour- Oceanography and Biochemistry taught extensively and brought in other sci- “ tesy of Joseph Mehling (Dartmouth College, Dunlap grew up in York, Pennsylvania as the entists to share what they had learned. It was an incredible smorgasbord of everything Hanover, NH). third of four children. He became an Eagle ” Scoutandwaschosenasoneofadozen that was going on in the field of rhythms, Dunlap says, “and an introduction to every- for Scouting’sNationalExplorationAward, insensitive to ambient temperature or nutri- body who was doing it.” which required applicants to write essays tion. “By sticking to a restricted definition,” Pittendrigh, Hastings, and other chrono- about their career goals. Dunlap had explored says Dunlap, “much of the biological noise biologists had made great strides in rhythms biochemistry at a summer program for high that came from loosely considering non- research beginning in the 1950s but had also school students at Ohio University and imag- circadian developmental or metabolic cycles “ run up against roadblocks. First, although ined a goal of studying biochemical ocean- fell away. With a defined phenotype you can ” therewereempiricalgeneralizationsabout ography. Earning the award, he says, do genetics” (2). circadian rhythms as biological cycles with solidified his interest in oceanography and Second, the research was hampered by a aperiodofaboutaday(1),thefieldlacked led him to attend the University of Wash- lack of molecular biological tools. As Dunlap a rigorous means to exclude extraneous ington beginning in 1970. began his postdoctoral fellowship with Jerry ’ rhythmic but noncircadian processes. “With After earning bachelors degrees in ocean- Feldman at the University of California, that loose definition, you end up pulling in ography and chemistry in 1974, Dunlap was Santa Cruz in 1979, he began laying the all sorts of biology that has no common admitted to two prominent oceanography groundwork for pushing through this molecular basis,” Dunlap says. graduate schools: Scripps Institution for roadblock. Oceanography and Woods Hole Oceano- “The most important thing to my mind,” graphic Institution. On the suggestion of a Dunlap says, “was restricting the phenotype Building and Winding a Clock friend, Dunlap also interviewed at Harvard to what we now consider in the strict sense a Dunlap aimed at elucidating the genetic and met J. Woodland “Woody” Hastings, circadian rhythm. This effort by Hastings, and molecular mechanism of the clock and whose research on bioluminescence in sin- Pittendrigh, and others made my work pos- the circadian system. A handful of circadian ” gle-celled dinoflagellates had led to an inves- sible. A circadian rhythm, as it has come to clock-related mutant gene loci had been tigation of the circadian clock elements of be defined, has a period around 24 hours previously identified in Chlamydomonas the dinoflagellates’ light show. Dunlap was under constant conditions. The timing of fascinated. “My rationalization was that I peaks and troughs in the cycle can be moved This is a Profile of a recently elected member of the National could study a marine organism and learn by exposure to real-world time cues, like light Academy of Sciences to accompany the member’s Inaugural biochemistry and physiology, and then go and temperature, but the period is relatively Article on page 16995 in issue 48 of volume 111. www.pnas.org/cgi/doi/10.1073/pnas.1514590112 PNAS | September 22, 2015 | vol. 112 | no. 38 | 11745–11747 Downloaded by guest on September 27, 2021 chromosome walk through the Neurospora the genes involved would be organism- genome, examining short DNA sequences specific, they put forth that the organizing and reintroducing them into Neurospora to principles of clock–gene output regulation identify the sequence that altered the fungus’ would be similar in all eukaryotes. circadian behavior. Meanwhile, Loros, work- ing at Dartmouth as a postdoctoral fellow, Clock-Controlled Genes began the first screens for clock-controlled For the Inaugural Article by Dunlap and genes or ccgs, which have products that are coworkers (12), he and his colleagues col- involved in circadian output rather than laborated with the US Department of Energy the core circadian mechanism. The frq gene to perform high-throughput RNA sequenc- was cloned in 1986, and the first ccgs were ing on Neurospora cells over the course of found in 1987, with both results published two days under constant conditions. The in 1989 (4, 5). The cloning of frq was results, he says, indicate multiple overlapping featured on the cover of Nature,thefirst levels of regulation for fine-tuning clock- of seven journal covers featuring the regulated gene expression. “There are genes work by Dunlap and Loros. These genes whose expression is active at one time of day provided the molecular entrée into the but whose RNA products peak much later,” circadian system. he says. “There are genes whose expression is Dunlap notes that the logic underlying cyclical, but whose gene product is steadily circadian clocks in fungi and animals is quite present, and genes that are expressed con- ” Jay C. Dunlap and Jennifer Loros in 2009 similar. Both are driven by a feedback loop, stantly, but whose products are rhythmic. Up to 40% of Neurospora’s genes may be with the genetic and physical map of Neu- in which two proteins constitute a hetero- dimericgeneswitchthatdrivesexpressionof controlled by the circadian clock, he found. rospora. Photo courtesy of Jon Gilbert Fox one or more genes, and those gene products, Daytime-transcribed genes were typically re- (photographer). in turn, act as negative elements to depress lated to metabolism, whereas nighttime genes the activity of the transcription factor (6). were involved in cell growth. The result, he says, is cyclical expression of green algae, fruit flies, and Neurospora crassa, Championing Neurospora the filamentous fungus used by the renowned frq, detectable by levels of the prototypic Dunlap and Loros have remained at Dart- geneticists Beadle and Tatum (3) to develop protein FRQ. After the elements of the mouth’s Geisel School of Medicine while their 1941 “one gene-one enzyme” hypothesis feedback loop began to fall into place, Dunlap andLoroscouldaskhowreal-worldtime raising their two children and mentoring of genetic function (3). At the time, only one more than 40 students and postdoctorate of the three organisms, Neurospora, could be cues, like light, can reset the clock. They found that exposure to light promoted the students, nearly two-thirds of whom have genetically transformed. Therefore, Dunlap “ ’ expression of frq.Furthermore,exposureto entered academia. It snowonderwefound began his study of the fungus that continues ” “ light at different points of the feedback loop out so much, he says, given such terrific today. “It’sawonderfulorganism,” he says, ” could shift the phase of the circadian cycle. people to work with. Dunlap also serves with well-defined genetic tools that make the ’ For example, early light exposure while frq as the first chair of the school s Genetics genome of Neurospora relatively simple to levels were increasing could bring frq mRNA Department, which was organized in the manipulate. However, Dunlap says, “It’sbi- levels to their peak immediately instead of late-1990s. ologically complex enough to be interesting.” at a later time, thereby advancing clock In the mid-1990s, Dunlap and Loros began During his postdoctoral fellowship, Dun- phase. Similarly, late exposure to light could work on a textbook with the goal of codifying lap learned basic molecular techniques and restimulate frq mRNA production and effect the field of rhythms biology, and the final worked closely with biology graduate stu- a phase delay. The result had broad signifi- effort drew significant help from chronobi- dents, including Jennifer Loros. Loros and cance, because clocks in both Neurospora and ology pioneer Patricia DeCoursey. Published Dunlap later forged a permanent partnership, mammals are reset through light induction in 2004 as Chronobiology: Biological Time- marrying in 1984.
Recommended publications
  • Crystal Structure of the Avirulence Gene Avrlm4-7 of Leptosphaeria Maculans. Illuminates Its Evolutionary and Functional Charact
    Crystal structure of the Avirulence Gene AvrLm4-7 of Leptosphaeria maculans. Illuminates its evolutionary and functional characteristics Isabelle Fudal, Francoise Blaise, K Blondeau, M. Graille, A. Labarde, A. Doisy, Bm Tyler, S.D. Kale, Guillaume Daverdin, Marie-Helene Balesdent, et al. To cite this version: Isabelle Fudal, Francoise Blaise, K Blondeau, M. Graille, A. Labarde, et al.. Crystal structure of the Avirulence Gene AvrLm4-7 of Leptosphaeria maculans. Illuminates its evolutionary and functional characteristics. 26. Fungal Genetics Conference at Asilomar, Mar 2011, Asilomar, United States. pp.234. hal-01000740 HAL Id: hal-01000740 https://hal.archives-ouvertes.fr/hal-01000740 Submitted on 6 Jun 2020 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. 26th Fungal Genetics Conference at Asilomar March 15-20 2011 Principle Financial Sponsors Genetics Society of America Burroughs Wellcome Fund US National Institutes of Health Novozymes Great Lakes Bioenergy Research Center Konkuk University Bio Molecular Informatics Center Genencor, A Danisco Division
    [Show full text]
  • Abstracts from the Neurospora 2002 Conference
    Fungal Genetics Reports Volume 49 Article 13 Abstracts from the Neurospora 2002 conference Neurospora 2002 conference Follow this and additional works at: https://newprairiepress.org/fgr This work is licensed under a Creative Commons Attribution-Share Alike 4.0 License. Recommended Citation Neurospora 2002 conference. (2002) "Abstracts from the Neurospora 2002 conference," Fungal Genetics Reports: Vol. 49, Article 13. https://doi.org/10.4148/1941-4765.1195 This Supplementary Material is brought to you for free and open access by New Prairie Press. It has been accepted for inclusion in Fungal Genetics Reports by an authorized administrator of New Prairie Press. For more information, please contact [email protected]. Abstracts from the Neurospora 2002 conference Abstract Abstracts and Poster abstracts from the Neurospora 2002 conference This supplementary material is available in Fungal Genetics Reports: https://newprairiepress.org/fgr/vol49/iss1/13 : Abstracts from the Neurospora 2002 conference Neurospora 2002 Schedule March 14-17, 2002 Invited Abstracts Asilomar Conference Center Pacific Grove, CA. Poster Abstracts SCIENTIFIC PROGRAM Index Barry Bowman Gloria Turner Schedule of Activities Thursday, March 14 3:00 - 6:00 pm, Registration: Administration 6:00 - 7:00 pm, Dinner: Crocker 7:00 - 10:00 pm, Mixer: Kiln Friday, March 15 7:30 - 8:30 am, Breakfast, Crocker 8:30 - 12:00 Noon, Session I, Chapel Genomic Analysis : Mary Anne Nelson, Chair 8:35 - Bruce Birren, MIT, Whitehead Institute. "Genome sequencing for Neurospora crassa." 9:05 - Gertrud Mannhaupt, Heinrich-Heine-University. "The MIPS Neurospora crassa database- MNCDB." 9:30 - Chuck Staben, U. of Kentucky. "Gene finding and annotation for fungal genomes." 9:55 - Alan Radford, University of Leeds.
    [Show full text]
  • Neurospora 2018 OCTOBER 18-21 ASILOMAR CONFERENCE CENTER
    PROGRAM and ABSTRACTS Neurospora 2018 OCTOBER 18-21 ASILOMAR CONFERENCE CENTER PACIFIC GROVE CALIFORNIA Cover design by Stephanie Herzog, Technische Universität Braunschweig Neurospora 2018 October 18-21 Asilomar Conference Center Pacific Grove California Scientific Organizers André Fleißner Thomas M. Hammond Technische Universität Braunschweig Illinois State University Neurospora Policy Committee Barry Bowman Jason E. Stajich Molecular Cell & Developmental Biology Dept. Plant Pathology & Microbiology University of California - Santa Cruz University of California - Riverside André Fleißner Thomas M. Hammond Institut für Genetik School of Biological Sciences Technische Universität Braunschweig Illinois State University Brief Schedule Morning Afternoon Evening Thursday Arrival Dinner October 18 Registration Mixer (Heather) Breakfast Lunch Friday Plenary Session I Plenary Session II Dinner October 19 Cell Biology and Metabolism, Signaling and Poster Session Morphogenesis Development Breakfast Lunch Banquet Saturday Plenary Session III Plenary Session IV Speaker October 20 Gene Expression and Genomics, Evolution, and Poster Session Epigenetics Tools Breakfast Sunday Plenary Session V Lunch October 21 Circadian Clocks and Departure Environmental Sensing All Plenary Sessions will be held in Heather. Posters will be displayed in Heather and Toyon throughout the meeting. They should be set up Friday and displayed until the end of the poster session/reception on Saturday evening. Schedule of Activities Thursday, October 18 15:00 - 18:00 p.m. Registration:
    [Show full text]
  • A Fungus Amongst Us 7
    Curr. Issues Mol. Biol. 16: 7-8. A Fungus Amongst Us 7 Book review Neurospora: Genomics and Molecular Biology Durgadas P. Kasbekar and Kevin McCluskey (Eds.) Caister Academic Press (2013) ISBN: 978-1-908230-12-6 A Fungus Amongst Us Neurospora Genomics and Molecular Biology Neurospora Genomics and Molecular Biology Neurospora Building on over 70 years of genetics research, Neurospora continues to be the leading model for the study of the genomics and molecular biology of flamentous Genomics and Molecular Biology fungi. The ease of culture, amenability to genetic and molecular genetic analysis, and the close correlation between genetic and biochemical traits are some of its Jennifer Loros advantages. Research with Neurospora has provided insights unachievable from work with simpler systems and difcult to extract from more complicated ones, cementing its position as a leading model system. In recent years the application of modern high throughput analyses had led to a deluge of information on the Department of Biochemistry, Thegenomics andAudrey molecular biology and of Neurospora Theodor. This timely book aims to distil the most important fndings to provide a snapshot of the current research landscape. Geisel School of Medicine at InDartmouth this book, internationally recognizedHanover, Neurospora experts NH, critically review the most important research and demonstrate the breadth of applications to industrial USA biology, biofuels, agriculture, and human health. The opening chapter is an introduction to the organism. Following chapters cover topics such as: carotenoid biosynthesis, polysaccharide deconstruction, genome biology, genome recombination, gene regulation, signal transduction, self-recognition, development, circadian rhythms and mutation. The book closes with a fascinating look at the Durgadas Kasbekar and Kevinhistory and futureMcCluskey trends for research have edited on Neurospora gene and genome Kasbekar and McCluskey Kasbekar an engaging new book calledanalysis.
    [Show full text]
  • The Light Mutant Oscillator (Lmo): a Novel Circadian
    THE LIGHT MUTANT OSCILLATOR (LMO): A NOVEL CIRCADIAN OSCILLATOR IN NEUROSPORA CRASSA A Thesis by HE HUANG Submitted to the Office of Graduate Studies of Texas A&M University in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE August 2008 Major Subject: Biology THE LIGHT MUTANT OSCILLATOR (LMO): A NOVEL CIRCADIAN OSCILLATOR IN NEUROSPORA CRASSA A Thesis by HE HUANG Submitted to the Office of Graduate Studies of Texas A&M University in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE Approved by: Chair of Committee, Deborah Bell-Pedersen Committee Members, Daniel Ebbole Susan Golden Wayne Versaw Head of Department, Vincent Cassone August 2008 Major Subject: Biology iii ABSTRACT The Light Mutant Oscillator (LMO): A Novel Circadian Oscillator in Neurospora crassa. (August 2008) He Huang, B.Eng., Beijing University of Chemical Technology Chair of Advisory Committee: Dr. Deborah Bell-Pedersen Circadian clocks are present in most eukaryotes and some prokaryotes and control rhythms in behavior, physiology and gene expression. One well-characterized circadian clock is that of Neurospora crassa. In addition to the well-described N. crassa FRQ/WCC oscillator, several lines of evidence have implied the presence of other oscillators which may have important functions in the N. crassa circadian clock system. However, the molecular details are only known for the core FRQ/WCC oscillator. The light mutant oscillator (LMO) was identified by two mutations (LM-1 and LM-2) and shown to control developmental rhythms in constant light (LL), conditions in which the FRQ/WCC oscillator is not functional. The objective of this project was to determine whether the developmental rhythms driven by the LMO are circadian, whether the components of the LMO communicate with components of the FRQ/WCC oscillator, and to begin to define the molecular nature of the LMO.
    [Show full text]
  • Neurospora 2004 Conference
    Fungal Genetics Reports Volume 51 Article 16 Abstracts from the Neurospora 2004 conference Neurospora Conference Follow this and additional works at: https://newprairiepress.org/fgr This work is licensed under a Creative Commons Attribution-Share Alike 4.0 License. Recommended Citation Neurospora Conference. (2004) "Abstracts from the Neurospora 2004 conference," Fungal Genetics Reports: Vol. 51, Article 16. https://doi.org/10.4148/1941-4765.1146 This Supplementary Material is brought to you for free and open access by New Prairie Press. It has been accepted for inclusion in Fungal Genetics Reports by an authorized administrator of New Prairie Press. For more information, please contact [email protected]. Abstracts from the Neurospora 2004 conference Abstract Abstracts from the Neurospora 2004 conference This supplementary material is available in Fungal Genetics Reports: https://newprairiepress.org/fgr/vol51/iss1/16 : Abstracts from the Neurospora 2004 conference Fungal Genetics Reports Volume 51 Article 16 Abstracts from the Neurospora 2004 conference Neurospora Conference Follow this and additional works at: http://newprairiepress.org/fgr Recommended Citation Neurospora Conference. (2004) "Abstracts from the Neurospora 2004 conference," Fungal Genetics Reports: Vol. 51, Article 16. https://dx.doi.org/10.4148/1941-4765.1146 This Supplementary Material is brought to you for free and open access by New Prairie Press. It has been accepted for inclusion in Fungal Genetics Reports by an authorized administrator of New Prairie Press. For more information, please contact [email protected]. Published by New Prairie Press, 2017 1 Fungal Genetics Reports, Vol. 51 [2004], Art. 16 Abstracts from the Neurospora 2004 conference Abstract Abstracts from the Neurospora 2004 conference Creative Commons License This work is licensed under a Creative Commons Attribution-Share Alike 4.0 License.
    [Show full text]
  • SRBR 2004 Program Book
    Ninth Meeting Society for Research on Biological Rhythms Program and Abstracts SRS/SRBR June 23, 2004 SRBR June 24–26, 2004 Whistler Resort • Whistler, British Columbia SOCIETY FOR RESEARCH ON BIOLOGICAL RHYTHMS i Executive Committee Editorial Board Ralph E. Mistleberger Simon Fraser University Steven Reppert, President Serge Daan University of Massachusetts Medical University of Groningen School Larry Morin SUNY, Stony Brook Bruce Goldman William Schwartz, President-Elect University of Connecticut University of Massachusetts Medical Hitoshi Okamura Kobe University School of Medicine School Terry Page Vanderbilt University Carla Green, Secretary Steven Reppert University of Massachusetts Medical University of Virginia Ueli Schibler School University of Geneva Fred Davis, Treasurer Mark Rollag Northeastern University Michael Terman Uniformed Services University Columbia University Helena Illnerova, Member-at-Large Benjamin Rusak Czech. Academy of Sciences Advisory Board Dalhousie University Takao Kondo, Member-at-Large Timothy J. Bartness Nagoya University Georgia State University Laura Smale Michigan State University Anna Wirz-Justice, Member-at-Large Vincent M. Cassone Centre for Chronobiology Texas A & M University Rae Silver Columbia University Journal of Biological Russell Foster Rhythms Imperial College of Science Martin Straume University of Virginia Jadwiga M. Giebultowicz Editor-in-Chief Oregon State University Elaine Tobin Martin Zatz University of California, Los Angeles National Institute of Mental Health Carla Green University of Virginia Fred Turek Associate Editors Northwestern University Eberhard Gwinner Josephine Arendt Max Planck Institute G.T.J. van der Horst University of Surrey Erasmus University Paul Hardin Michael Hastings University of Houston David R. Weaver MRC, Cambridge University of Massachusetts Medical Helena Illerova Center Ken-Ichi Honma Czech.
    [Show full text]
  • General Information
    General Information Headquarters is at the Baytowne Conference Center, which is conveniently located within walking distance of all hotel rooms. SRBR Information Desk and Message Center is in the Foyer of the Baytowne Conference Center main level. The desk hours are as follows: Friday 5/21 2:00–6:00 PM Saturday 5/22 7:30 –11:00 AM 2:00–8:00 PM Sunday 5/23 7:00–11:00 AM 4:00–7:00 PM Monday 5/24 7:30–11:00 AM 4:00–6:00 PM Tuesday 5/25 8:00–11:00 AM 4:00–6:00 PM Wednesday 5/26 8:00–10:00 AM Messages can be left on the SRBR message board next to the registration desk. Meeting participants are asked to check the message board routinely for mail, notes, and telephone messages. Hotel check-in will be at the individual properties. Posters will be available for viewing in the Magnolia B/C/D/E rooms. Poster numbers 1–93 Sunday, May 23, 10:00 AM–10:30 PM Poster numbers 94–183 Monday, May 24, 10:00 AM–10:30 PM Poster number 184–275 Tuesday, May 25, 10:00 AM–10:30 PM All posters must be removed by 10:00 am on Wednesday, May 26. The Village of Baytowne Wharf—Indulge your senses at Sandestin’s charming Village of Baytowne Wharf, a picturesque pedestrian village overlooking the Choctawatchee Bay. Discover a unique collection of more than 40 specialty merchants ranging from quaint boutiques and intimate eateries to lively nightclubs, all set up against a backdrop of vibrant special events.
    [Show full text]
  • Abstracts from the Neurospora 2006 Conference
    Fungal Genetics Reports Volume 53 Article 16 Abstracts from the Neurospora 2006 Conference Neurospora Conference Follow this and additional works at: https://newprairiepress.org/fgr This work is licensed under a Creative Commons Attribution-Share Alike 4.0 License. Recommended Citation Neurospora Conference. (2006) "Abstracts from the Neurospora 2006 Conference," Fungal Genetics Reports: Vol. 53, Article 16. https://doi.org/10.4148/1941-4765.1119 This Supplementary Material is brought to you for free and open access by New Prairie Press. It has been accepted for inclusion in Fungal Genetics Reports by an authorized administrator of New Prairie Press. For more information, please contact [email protected]. Abstracts from the Neurospora 2006 Conference Abstract Plenary and poster session abstracts from the Neurospora 2006 Conference This supplementary material is available in Fungal Genetics Reports: https://newprairiepress.org/fgr/vol53/iss1/16 : Abstracts from the Neurospora 2006 Conference NEUROSPORA 2006 PLENARY SESSION ABSTRACTS Session I: From Genes to Populations Tony Griffiths, Chair Control of DNA Methylation in Neurospora Eric Selker, Institute of Molecular Biology, University of Oregon, Eugene, OR 97403-1229 Most methylated regions of Neurospora are products of RIP (repeat-induced point mutation), a premeiotic homology-based genome defense system that litters duplicated sequences with C:G to T:A mutations and typically leaves them methylated at remaining cytosines. I will present our current understanding about how A:T-rich DNA, such as that resulting from RIP, triggers methylation. Our efforts to elucidate the control of DNA methylation in vegetative cells have revealed mechanistic ties between modifications of DNA and histones.
    [Show full text]
  • The 2009 George W. Beadle Award Jay C. Dunlap
    Honors and Awards 831 The 2009 George W. Beadle Award Jay C. Dunlap Jay C. Dunlap HE 2009 George W. Beadle Medal for outstanding California at Santa Cruz and joined Jerry Feldman’s T contributions to the genetics community is group. Feldman was the leading Neurospora geneticist awarded to Jay C. Dunlap. This award is a tribute to studying the biological clock. He and his colleagues had Jay’s pioneering studies on the circadian clock and the isolated mutant strains with altered circadian periods in Neurospora crassa frequency ( frq) gene—the first micro- the developmental rhythm (Feldman and Hoyle 1973). bial clock gene to be cloned (McClung et al. 1989). Jay’s arrival coincided with the newly emerging recombi- Jay’s work on the genetics of circadian rhythms came at nant DNA techniques being developed for Neurospora a time when the field of chronobiology was still in its (Case et al. 1979; Kinnaird and Fincham 1983; infancy and when the research focused primarily on the Schechtman and Yanofsky 1983). It was his goal to physiology and anatomy of the clock. It was widely learn the tools of molecular and Neurospora biology, with believed that genetic approaches to understanding the the hopes of cloning the clock genes. Jay ultimately clock were intractable and that clocks evolved in- succeeded in cloning a clock gene after taking a position dependently in different organisms (Pittendrigh as an assistant professor of biochemistry at Dartmouth 1993). Thus, it was thought that studying the clock in Medical School. His group cloned the frq gene using a fungi or other microbes would not reveal the mecha- chromosome walk and showed that the cloned DNA nism used by the mammalian clock.
    [Show full text]
  • SRBR 2012 Program
    SRBR 2012 Program Saturday, May 19, 2012 9:00-5:00 PM Trainee Professional Development Day 7:00-9:00 PM Opening Reception * Grand Lawn Sunday, May 20, 2012 8:15-10:00 AM Symposium 1: Signal Integration In Circadian Neural Networks Chair: Sato Honma, Hokkaido University Speakers: David Welsh, University of California, San Diego Elizabeth Maywood, MRC Laboratory of Molecular Biology, Cambridge Mark Zoran, Texas A&M University Paul Taghert, Washington University Medical School Symposium 2: Translational Chronobiology Chair: Francis Levi, INSERM Speakers: Karla Allebrandt, Ludwig-Maximilians-University of Munich Steven Brown, University of Zurich Pasquale Innominato, INSERM Francesco Benedetti, University of Modena Symposium 3: The Molecular Clockworks Chair: Luis Larrondo, P. Universidad Catolica de Chile Speakers: Paul Hardin, Texas A&M University Felix Naef, Ecole Polytechique Federale de Lausanne Steve Kay, University of California, San Diego Michael Brunner, Heidelburg University 11:00 – 12:30 PM Slide Session A 12:30 – 4:15 PM Free Time, Workshops 4:15 – 6:30 PM Symposium 4: New Discoveries in the TTFL Chair: Yi Liu, UT Southwestern Medical Center Speakers: Ueli Schibler, University of Geneva Ravi Allada, Northwestern University Joanna Chiu, University of California, Davis David Somers,,Ohio State University/POSTECH Symposium 5: Time to Sleep Chair: Valérie Mongrain, University of Montreal and CARSM Speakers: Michael Nitabach, Yale School of Medicine Paul Franken, University of Lausanne Helen Burgess, Rush University Medical Center
    [Show full text]
  • SRBR 2010 Program Saturday, May 22, 2010 7:00–9:00 Pm Opening
    SRBR 2010 Program Saturday, May 22, 2010 7:00–9:00 pm Opening reception Sunday, May 23, 2010 8:30–10:30 am Symposium 1–Transcriptional Regulation of Circadian Clocks Chair: Stacey Harmer, University of California, Davis 8:30 The molecular mechanism of photoadaptation and light entrainment of the Neurospora clock Michael Brunner, Heidelberg University 9:00 Novel approaches for studying circadian transcription in cells and organs Ueli Schibler, University of Geneva 9:30 Molecular mechanism of the drosophila clock Amita Sehgal, HHMI/University of Pennsylvania School of Medicine 10:00 Identification of a new circadian component using data mining Stacey Harmer, University of California, Davis Symposium 2–Circadian Neural Networks Chair: Fernanda Ceriani, Leloir Institute Foundation-Buenos Aires 8:30 CRYPTOCHROME is a cell autonomous neuronal blue light sensor that rapidly regulates neuronal firing rate Todd Holmes, University of California, Irvine 9:00 Accessing neural connectivity in the Drosophila circadian clock network Orie Shafer, University of Michigan 9:30 Complex Electrical States of SCN Neurons Hugh Piggins, University of Manchester 10:00 A parallel circadian system: Making sense of olfactory clocks Erik Herzog, Washington University 10:30–11:00 am Refreshment Break 11:00 am–12:30 pm Slide Session A Chair: Martin Ralph, University of Toronto 11:00 1 • USP2, a de-ubiquitinating enzyme, directly regulates BMAL1 stability and sensitivity to early evening light Heather Scoma, CBNA, Medical College of Wisconsin, Milwaukee, Wisconsin, United States 11:15 2 • The deubiquitinating enzyme USP2 is involved in the regulation of circadian rhythms Adeline Rachalski, Laboratory of Molecular Chronobiology, Douglas Mental Health Institute, Montréal, Canada 11:30 3 • Circadian rhythms in astrocytes depend on intercellular interactions and connexin 43 Luciano Marpegan, Biology, Washington University, St.
    [Show full text]