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David Glover

David Moore Glover FRS FRSE (born 28 March 1948) is a British geneticist and Research Professor of Biology and Biological Engineering at the California Institute of Technology.[4] He served as Balfour Professor of Genetics at the University of Cambridge, a Wellcome Trust investigator in the Department of Genetics at the University of Cambridge, and Fellow of Fitzwilliam College, Cambridge. He serves as the first editor-in-chief of the open-access journal Open Biology published by the Royal Society.[5][6][7][3][2][8]

David Glover

Born
David Moore Glover

(1948-03-28) March 28, 1948 (age 75)[3]
NationalityBritish
EducationBroadway Technical Grammar School, Barnsley[3]
Alma materUniversity of Cambridge (BA, ScD)
University of London (PhD)
Spouse
(m. 2000)
AwardsEMBO Member (1978)[1]
Scientific career
FieldsMitosis
Meiosis
Centrosomes[2]
InstitutionsImperial Cancer Research Fund
University College London
Stanford University
Imperial College
University of Dundee
University of Cambridge
California Institute of Technology
ThesisThe synthesis of polyoma virus specific RNA in mouse cells

Education edit

Glover was educated at Broadway Technical Grammar School, Barnsley[3] and the University of Cambridge.[3] He undertook his PhD research in the Imperial Cancer Research Fund laboratories as a student of University College London.[9]

Career and research edit

As a Damon Runyon Fellow at Stanford University he participated in the Recombinant DNA revolution and discovered sequences that interrupted the ribosomal genes of Drosophila. On establishing his independent laboratory at Imperial College London in 1975, he later showed that these were ancient transposable elements. Together with Peter Rigby, Jean Beggs and David Lane, he co-directed a combined research group exploiting the new techniques of recombinant DNA research. In 1978 he was elected Member of the European Molecular Biology Organization (EMBO).[1]

While at Imperial, Glover was awarded a 10-year personal fellowship from the UK's Cancer Research Campaign that allowed him open up a new area of research pioneering the use of Drosophila as a model in which to study cell cycle regulation. He began by characterising the duplication cycles of centrosomes in the rapid nuclear division cycles of Drosophila embryos. This led to genetic studies that allowed him to discover and name the Polo and Aurora protein kinases, required for the function of centrosomes at the poles of mitotic spindles.[10]

In 1989, he relinquished his position as Head of the Department of Biochemistry at Imperial to move to the University of Dundee, where with David and Birgitte Lane he established the Cancer Research Campaign Laboratories, Dundee. Here his work demonstrated Polo not only to be required at centrosomes in Drosophila but also for cytokinesis. In parallel studies, Glover found that in an organism as distant as fission yeast, Polo's counterpart, that he named Plo1, was also required to establish functional spindle pole bodies and cytokinesis rings. Remarkably, the localisation and function of Polo kinase at the centrosome, the kinetochore and the central spindle in cytokinesis was highly conserved in human cells where its expression was elevated in tumours. This led Glover to collaborations with Biotechnological and Pharmaceutical industries in developing small molecule inhibitors of Polo for use in cancer therapy.[citation needed]

In Dundee he continued to use Drosophila as a means to uncover new components of the mitotic apparatus and its regulatory circuits. These studies uncovered spindle pole molecules whose functions were regulated by Polo kinase; a germ line specific Cdc25 phosphatase that regulates meiotic entry; and demonstrated the roles of PP1 and PP2A protein phosphatases as negative mitotic regulators. His contribution to science in Scotland was recognised by his election to Fellow of the Royal Society of Edinburgh (FRSE).[citation needed]

In 1999, Glover moved to the University of Cambridge to become the 6th Arthur Balfour Professor of Genetics and Head of Department. In Cambridge he discovered the second main Aurora B kinase required for cells to progress through metaphase and used genetic approaches to identify and demonstrate the roles of the Greatwall kinase in inhibiting protein phosphase 2A during mitotic entry and progression. Over the past decade he has uncovered the major steps of centriole duplication by demonstrating that Polo-like-kinase 4 (Plk4) is its master regulator; Plk4 expression can drive the de novo formation of centrioles in unfertilised Drosophila eggs. In searching for Plk4's partners, his group identified Asterless (Cep152 in human cells) as required for bringing Plk4 to centrioles and an F-box protein, Slimb – a component of the SCF ubiquitin protein ligase, as responsible for targeting excess Plk4 for destruction. They showed that Plk4 phosphorylates the centriole protein Ana2/STIL to enable it to bind the "cartwheel protein" Sas6 and thus initiate procentriole formation, the first step of centriole duplication.[citation needed]

In 2019, the Glover Lab moved to the California Institute of Technology in USA. [11]

Glover's group are now[when?] studying the consequences of supernumerary centrosomes in a variety of mammalian tissues and their consequences for the balance of cell proliferation and differentiation in the skin and pancreas.

Personal life edit

Glover married Magdalena Żernicka-Goetz in 2000.[3]

References edit

  1. ^ a b "David M. Glover". people.embo.org.
  2. ^ a b David Glover publications indexed by Google Scholar  
  3. ^ a b c d e f Anon (2017). "Glover, Prof. David Moore". Who's Who (online Oxford University Press ed.). Oxford: A & C Black. doi:10.1093/ww/9780199540884.013.U17298. (Subscription or UK public library membership required.)
  4. ^ Glover DM; Leibowitz MH; McLean DA; Parry H (7 April 1995). "Mutations in aurora prevent centrosome separation leading to the formation of monopolar spindles". Cell. 81 (1): 95–105. doi:10.1016/0092-8674(95)90374-7. ISSN 0092-8674. PMID 7720077. Wikidata Q29617537.
  5. ^ Press release by the Royal Society on the launch of the journal, 17 October 2011 ()
  6. ^ . Archived from the original on 15 June 2011. Retrieved 11 June 2011.
  7. ^ . debretts.com. Archived from the original on 8 September 2012.
  8. ^ David Glover publications from Europe PubMed Central
  9. ^ Glover, David Moore (1972). The synthesis of polyoma virus specific RNA in mouse cells (PhD thesis). University College London (University of London). OCLC 857995843. EThOS uk.bl.ethos.574633.
  10. ^ R Giet; David Glover (1 February 2001). "Drosophila aurora B kinase is required for histone H3 phosphorylation and condensin recruitment during chromosome condensation and to organize the central spindle during cytokinesis". Journal of Cell Biology. 152 (4): 669–682. doi:10.1083/JCB.152.4.669. ISSN 0021-9525. PMC 2195771. PMID 11266459. Wikidata Q28206511.
  11. ^ "David Glover, Division of Biology and Biological Engineering, California Institute of Technology". Retrieved 19 October 2022.

david, glover, other, people, named, disambiguation, david, moore, glover, frse, born, march, 1948, british, geneticist, research, professor, biology, biological, engineering, california, institute, technology, served, balfour, professor, genetics, university,. For other people named David Glover see David Glover disambiguation David Moore Glover FRS FRSE born 28 March 1948 is a British geneticist and Research Professor of Biology and Biological Engineering at the California Institute of Technology 4 He served as Balfour Professor of Genetics at the University of Cambridge a Wellcome Trust investigator in the Department of Genetics at the University of Cambridge and Fellow of Fitzwilliam College Cambridge He serves as the first editor in chief of the open access journal Open Biology published by the Royal Society 5 6 7 3 2 8 David GloverFRS FRSEBornDavid Moore Glover 1948 03 28 March 28 1948 age 75 3 Chapeltown South YorkshireNationalityBritishEducationBroadway Technical Grammar School Barnsley 3 Alma materUniversity of Cambridge BA ScD University of London PhD SpouseMagdalena Zernicka Goetz m 2000 wbr AwardsEMBO Member 1978 1 Scientific careerFieldsMitosisMeiosisCentrosomes 2 InstitutionsImperial Cancer Research FundUniversity College LondonStanford UniversityImperial CollegeUniversity of DundeeUniversity of CambridgeCalifornia Institute of TechnologyThesisThe synthesis of polyoma virus specific RNA in mouse cells Contents 1 Education 2 Career and research 3 Personal life 4 ReferencesEducation editGlover was educated at Broadway Technical Grammar School Barnsley 3 and the University of Cambridge 3 He undertook his PhD research in the Imperial Cancer Research Fund laboratories as a student of University College London 9 Career and research editAs a Damon Runyon Fellow at Stanford University he participated in the Recombinant DNA revolution and discovered sequences that interrupted the ribosomal genes of Drosophila On establishing his independent laboratory at Imperial College London in 1975 he later showed that these were ancient transposable elements Together with Peter Rigby Jean Beggs and David Lane he co directed a combined research group exploiting the new techniques of recombinant DNA research In 1978 he was elected Member of the European Molecular Biology Organization EMBO 1 While at Imperial Glover was awarded a 10 year personal fellowship from the UK s Cancer Research Campaign that allowed him open up a new area of research pioneering the use of Drosophila as a model in which to study cell cycle regulation He began by characterising the duplication cycles of centrosomes in the rapid nuclear division cycles of Drosophila embryos This led to genetic studies that allowed him to discover and name the Polo and Aurora protein kinases required for the function of centrosomes at the poles of mitotic spindles 10 In 1989 he relinquished his position as Head of the Department of Biochemistry at Imperial to move to the University of Dundee where with David and Birgitte Lane he established the Cancer Research Campaign Laboratories Dundee Here his work demonstrated Polo not only to be required at centrosomes in Drosophila but also for cytokinesis In parallel studies Glover found that in an organism as distant as fission yeast Polo s counterpart that he named Plo1 was also required to establish functional spindle pole bodies and cytokinesis rings Remarkably the localisation and function of Polo kinase at the centrosome the kinetochore and the central spindle in cytokinesis was highly conserved in human cells where its expression was elevated in tumours This led Glover to collaborations with Biotechnological and Pharmaceutical industries in developing small molecule inhibitors of Polo for use in cancer therapy citation needed In Dundee he continued to use Drosophila as a means to uncover new components of the mitotic apparatus and its regulatory circuits These studies uncovered spindle pole molecules whose functions were regulated by Polo kinase a germ line specific Cdc25 phosphatase that regulates meiotic entry and demonstrated the roles of PP1 and PP2A protein phosphatases as negative mitotic regulators His contribution to science in Scotland was recognised by his election to Fellow of the Royal Society of Edinburgh FRSE citation needed In 1999 Glover moved to the University of Cambridge to become the 6th Arthur Balfour Professor of Genetics and Head of Department In Cambridge he discovered the second main Aurora B kinase required for cells to progress through metaphase and used genetic approaches to identify and demonstrate the roles of the Greatwall kinase in inhibiting protein phosphase 2A during mitotic entry and progression Over the past decade he has uncovered the major steps of centriole duplication by demonstrating that Polo like kinase 4 Plk4 is its master regulator Plk4 expression can drive the de novo formation of centrioles in unfertilised Drosophila eggs In searching for Plk4 s partners his group identified Asterless Cep152 in human cells as required for bringing Plk4 to centrioles and an F box protein Slimb a component of the SCF ubiquitin protein ligase as responsible for targeting excess Plk4 for destruction They showed that Plk4 phosphorylates the centriole protein Ana2 STIL to enable it to bind the cartwheel protein Sas6 and thus initiate procentriole formation the first step of centriole duplication citation needed In 2019 the Glover Lab moved to the California Institute of Technology in USA 11 Glover s group are now when studying the consequences of supernumerary centrosomes in a variety of mammalian tissues and their consequences for the balance of cell proliferation and differentiation in the skin and pancreas Personal life editGlover married Magdalena Zernicka Goetz in 2000 3 References edit a b David M Glover people embo org a b David Glover publications indexed by Google Scholar nbsp a b c d e f Anon 2017 Glover Prof David Moore Who s Who online Oxford University Press ed Oxford A amp C Black doi 10 1093 ww 9780199540884 013 U17298 Subscription or UK public library membership required Glover DM Leibowitz MH McLean DA Parry H 7 April 1995 Mutations in aurora prevent centrosome separation leading to the formation of monopolar spindles Cell 81 1 95 105 doi 10 1016 0092 8674 95 90374 7 ISSN 0092 8674 PMID 7720077 Wikidata Q29617537 Press release by the Royal Society on the launch of the journal 17 October 2011 WebCite Department of Genetics University of Cambridge Archived from the original on 15 June 2011 Retrieved 11 June 2011 Prof David M Glover FRS FRSE Authorised Biography Debrett s People of Today Prof David M Glover FRS FRSE Profile debretts com Archived from the original on 8 September 2012 David Glover publications from Europe PubMed Central Glover David Moore 1972 The synthesis of polyoma virus specific RNA in mouse cells PhD thesis University College London University of London OCLC 857995843 EThOS uk bl ethos 574633 R Giet David Glover 1 February 2001 Drosophila aurora B kinase is required for histone H3 phosphorylation and condensin recruitment during chromosome condensation and to organize the central spindle during cytokinesis Journal of Cell Biology 152 4 669 682 doi 10 1083 JCB 152 4 669 ISSN 0021 9525 PMC 2195771 PMID 11266459 Wikidata Q28206511 David Glover Division of Biology and Biological Engineering California Institute of Technology Retrieved 19 October 2022 Retrieved from https en wikipedia org w index php title David Glover amp oldid 1169384670, wikipedia, wiki, book, books, library,

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