Elizabeth Robertson

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Liz Robertson

Elizabeth Robertson.jpg
Born
Elizabeth Jane Robertson
Alma mater University of Oxford (BA, MA)
University of Cambridge (PhD)
Awards Royal Medal (2016)
EMBO Member (2002)
Suffrage Science award (2011)
Scientific career
Institutions Columbia University
Harvard University
University of Oxford
Doctoral advisor Martin Evans

Elizabeth Jane Robertson CBE FRS MAE is a British developmental biologist based at the Sir William Dunn School of Pathology, University of Oxford. [1] She is Professor of Developmental Biology [2] at Oxford and a Wellcome Trust Principal Research Fellow. [3] She is best known for her pioneering work in developmental genetics, showing that genetic mutations could be introduced into the mouse germ line by using genetically altered embryonic stem cells. [4] [5] This discovery opened up a major field of experimentation for biologists and clinicians. [6] [7] [8]

Contents

Education

Robertson earned her Bachelor of Arts degree from the University of Oxford. [9] She received a PhD from the University of Cambridge in 1982 under the supervision of Martin Evans. [10]

Career and research

After her PhD, she stayed on at the University of Cambridge for her postdoctoral fellowship and continued to work there as a research assistant following the completion of her fellowship. [11] She was a professor first at Columbia University and then Harvard University before moving to the University of Oxford. [11] In her lab at Columbia she was the first to show that embryonic stem cells carrying genetic mutations could contribute to all parts of the adult mouse body, including the cells that eventually make up the gametes, i.e. sperm and egg cells, allowing these mutations to be transmitted to the next generation. [4] [5] She used this approach to test the role of specific growth factors in embryonic development, [12] and to screen for previously unknown genes that prevent normal development. [13] [14] Robertson's work was among the first to show that the disruption of many genes has surprisingly little effect on development and organismal phenotype, [15] [16] [17] contributing to a long-running challenge in the understanding of the robustness of biological systems. She has also made significant contributions to the question of how the early embryo determines the anterior-posterior polarity that patterns the embryo from head to tail [18] [19] and the mechanisms that pattern the embryo from left to right. [20]

Robertson currently serves as an editor of the journal Development. [21] She serves on the editorial boards of Developmental Biology , [22] Current Opinion in Genetics & Development , [23] and Developmental Cell . [24]

Honours and awards

Robertson was appointed Commander of the Order of the British Empire (CBE) in the 2024 New Year Honours for services to medical sciences. [25]

Related Research Articles

<span class="mw-page-title-main">Chimera (genetics)</span> Single organism composed of two or more different populations of genetically distinct cells

A genetic chimerism or chimera is a single organism composed of cells with more than one distinct genotype. In animals and human chimeras, this means an individual derived from two or more zygotes, which can include possessing blood cells of different blood types, and subtle variations in form (phenotype). Animal chimeras are produced by the merger of two embryos. In plant chimeras, however, the distinct types of tissue may originate from the same zygote, and the difference is often due to mutation during ordinary cell division. Normally, genetic chimerism is not visible on casual inspection; however, it has been detected in the course of proving parentage. In contrast, an individual where each cell contains genetic material from two organisms of different breeds, varieties, species or genera is called a hybrid.

<span class="mw-page-title-main">Gastrulation</span> Stage in embryonic development in which germ layers form

Gastrulation is the stage in the early embryonic development of most animals, during which the blastula, or in mammals the blastocyst, is reorganized into a two-layered or three-layered embryo known as the gastrula. Before gastrulation, the embryo is a continuous epithelial sheet of cells; by the end of gastrulation, the embryo has begun differentiation to establish distinct cell lineages, set up the basic axes of the body, and internalized one or more cell types including the prospective gut.

<span class="mw-page-title-main">Germline</span> Population of a multicellular organisms cells that pass on their genetic material to the progeny

In biology and genetics, the germline is the population of a multicellular organism's cells that develop into germ cells. In other words, they are the cells that form gametes, which can come together to form a zygote. They differentiate in the gonads from primordial germ cells into gametogonia, which develop into gametocytes, which develop into the final gametes. This process is known as gametogenesis.

<span class="mw-page-title-main">Martin Evans</span> British biologist

Sir Martin John EvansFLSW is an English biologist who, with Matthew Kaufman, was the first to culture mice embryonic stem cells and cultivate them in a laboratory in 1981. He is also known, along with Mario Capecchi and Oliver Smithies, for his work in the development of the knockout mouse and the related technology of gene targeting, a method of using embryonic stem cells to create specific gene modifications in mice. In 2007, the three shared the Nobel Prize in Physiology or Medicine in recognition of their discovery and contribution to the efforts to develop new treatments for illnesses in humans.

<span class="mw-page-title-main">Anne McLaren</span> British scientist

Dame Anne Laura Dorinthea McLaren, was a British scientist who was a leading figure in developmental biology. She paved the way for women in science and her work helped lead to human in vitro fertilisation (IVF). She left an enduring legacy marked by her research and ethical contributions to the field. She received many honors for her contributions to science, including election as fellow of the Royal Society.

<span class="mw-page-title-main">Inner cell mass</span> Early embryonic mass that gives rise to the fetus

The inner cell mass (ICM) or embryoblast is a structure in the early development of an embryo. It is the mass of cells inside the blastocyst that will eventually give rise to the definitive structures of the fetus. The inner cell mass forms in the earliest stages of embryonic development, before implantation into the endometrium of the uterus. The ICM is entirely surrounded by the single layer of trophoblast cells of the trophectoderm.

Lefty are a class of proteins that are closely related members of the TGF-beta superfamily of growth factors. These proteins are secreted and play a role in left-right asymmetry determination of organ systems during development. Mutations of the genes encoding these proteins have been associated with left-right axis malformations, particularly in the heart and lungs.

In developmental biology, the cells that give rise to the gametes are often set aside during embryonic cleavage. During development, these cells will differentiate into primordial germ cells, migrate to the location of the gonad, and form the germline of the animal.

<span class="mw-page-title-main">Cripto</span> Protein-coding gene in the species Homo sapiens

Cripto is an EGF-CFC or epidermal growth factor-CFC, which is encoded by the Cryptic family 1 gene. Cryptic family protein 1B is a protein that in humans is encoded by the CFC1B gene. Cryptic family protein 1B acts as a receptor for the TGF beta signaling pathway. It has been associated with the translation of an extracellular protein for this pathway. The extracellular protein which Cripto encodes plays a crucial role in the development of left and right division of symmetry.

<span class="mw-page-title-main">Nodal homolog</span> Mammalian protein found in Homo sapiens

Nodal homolog is a secretory protein that in humans is encoded by the NODAL gene which is located on chromosome 10q22.1. It belongs to the transforming growth factor beta superfamily. Like many other members of this superfamily it is involved in cell differentiation in early embryogenesis, playing a key role in signal transfer from the primitive node, in the anterior primitive streak, to lateral plate mesoderm (LPM).

<span class="mw-page-title-main">Gail R. Martin</span> American biologist (born 1944)

Gail Roberta Martin is an American biologist. She is professor emerita in the Department of Anatomy, University of California, San Francisco. She is known for her pioneering work on the isolation of pluripotent stem cells from normal embryos, for which she coined the term 'embryonic stem cells'. She is widely recognized for her work on the function of fibroblast growth factors and their negative regulators in vertebrate organogenesis. She and her colleagues made contributions to gene targeting technology.

<span class="mw-page-title-main">Janet Rossant</span> Biologist

Janet Rossant, is a developmental biologist well known for her contributions to the understanding of the role of genes in embryo development. She is a world renowned leader in developmental biology. Her current research interests focus on stem cells, molecular genetics, and developmental biology. Specifically, she uses cellular and genetic manipulation techniques to study how genes control both normal and abnormal development of early mouse embryos. Rossant has discovered information on embryo development, how multiple types of stem cells are established, and the mechanisms by which genes control development. In 1998, her work helped lead to the discovery of the trophoblast stem cell, which has assisted in showing how congenital anomalies in the heart, blood vessels, and placenta can occur.

The Nodal signaling pathway is a signal transduction pathway important in regional and cellular differentiation during embryonic development.

<span class="mw-page-title-main">Allan Bradley</span> British geneticist

Allan Bradley FRS is a British geneticist at the Wellcome Trust Sanger Institute.

<span class="mw-page-title-main">Rosa Beddington</span> English developmental biologist

Rosa Susan Penelope Beddington FRS was a British biologist whose career had a major impact on developmental biology.

Margaret Buckingham, is a British developmental biologist working in the fields of myogenesis and cardiogenesis. She is an honorary professor at the Pasteur Institute in Paris and emeritus director in the Centre national de la recherche scientifique (CNRS). She is a member of the European Molecular Biology Organization, the Academia Europaea and the French Academy of Sciences.

Magdalena Żernicka-Goetz is a Polish-British developmental biologist. She is Professor of Mammalian Development and Stem Cell Biology in the Department of Physiology, Development and Neuroscience and Fellow of Sidney Sussex College, Cambridge. She also serves as Bren Professor of Biology and Biological Engineering at California Institute of Technology (Caltech).

Left-right asymmetry is the process in early embryonic development that breaks the normal symmetry in the bilateral embryo. In vertebrates, left-right asymmetry is established early in development at a structure called the left-right organizer and leads to activation of different signalling pathways on the left and right of the embryo. This in turn cause several organs in adults to develop LR asymmetry, such as the tilt of the heart, the different number lung lobes on each side of the body and the position of the stomach and spleen on the right side of the body. If this process does not occur correctly in humans it can result in the syndromes heterotaxy or situs inversus.

Peter Anthony Koopman is an Australian biologist best known for his role in the discovery and study of the mammalian Y-chromosomal sex-determining gene, Sry.

Marisa Bartolomei is an American cell biologist, the Perelman Professor of Cell and Developmental Biology and Co-Director of the Epigenetics Institute at the Perelman School of Medicine at the University of Pennsylvania. Her research considers epigenetic processes including genomic imprinting. She was elected to the National Academy of Sciences in 2021.

References

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  2. Liz Robertson Archived 6 November 2013 at the Wayback Machine , stemcells.ox.ac.uk; accessed 9 April 2018.
  3. Principal Research Fellows Archived 14 May 2016 at the Wayback Machine , wellcome.ac.uk; accessed 9 April 2018.
  4. 1 2 "Elizabeth Robertson | Royal Society". royalsociety.org. Retrieved 28 February 2019.
  5. 1 2 Schwartzberg, P. L.; Goff, S. P.; Robertson, E. J. (10 November 1989). "Germ-line transmission of a c-abl mutation produced by targeted gene disruption in ES cells". Science. 246 (4931): 799–803. Bibcode:1989Sci...246..799S. doi:10.1126/science.2554496. ISSN   0036-8075. PMID   2554496.
  6. Mak, T. W.; Penninger, J. M.; Ohashi, P. S. (2001). "Knockout mice: a paradigm shift in modern immunology". Nature Reviews. Immunology. 1 (1): 11–19. doi:10.1038/35095551. ISSN   1474-1733. PMID   11905810.
  7. Butler, A. A.; Cone, R. D. (2001). "Knockout models resulting in the development of obesity". Trends in Genetics. 17 (10): S50–54. doi:10.1016/S0168-9525(01)02481-7. ISSN   0168-9525. PMID   11585677.
  8. Smith, Austin G. (2001). "Embryo-Derived Stem Cells: Of Mice and Men". Annual Review of Cell and Developmental Biology. 17 (1): 435–462. doi:10.1146/annurev.cellbio.17.1.435. PMID   11687496. S2CID   30030832.
  9. Elizabeth Robertson: International Advisory Board in Developmental Biology, f1000.com; accessed 9 April 2018.
  10. "Elizabeth Robertson". Greengard Prize. Retrieved 28 February 2019.
  11. 1 2 3 4 Blank, Ann (2008). "Elizabeth Robertson Awarded Edwin G. Conklin Medal" (PDF). Society for Developmental Biology. SDB. Retrieved 4 March 2014.
  12. DeChiara, T. M.; Efstratiadis, A.; Robertson, E. J. (3 May 1990). "A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting". Nature. 345 (6270): 78–80. Bibcode:1990Natur.345...78D. doi:10.1038/345078a0. ISSN   0028-0836. PMID   2330056. S2CID   4343800.
  13. Conlon, F. L.; Barth, K. S.; Robertson, E. J. (1991). "A novel retrovirally induced embryonic lethal mutation in the mouse: assessment of the developmental fate of embryonic stem cells homozygous for the 413.d proviral integration". Development. 111 (4): 969–981. doi:10.1242/dev.111.4.969. ISSN   0950-1991. PMID   1879365.
  14. Robertson, E. J.; Conlon, F. L.; Barth, K. S.; Costantini, F.; Lee, J. J. (1992). "Use of Embryonic Stem Cells to Study Mutations Affecting Postimplantation Development in the Mouse". Ciba Foundation Symposium 165 - Postimplantation Development in the Mouse. Novartis Foundation Symposia. Vol. 165. pp. 237–250, discussion 250–255. doi:10.1002/9780470514221.ch14. ISBN   9780470514221. ISSN   0300-5208. PMID   1516471.{{cite book}}: |journal= ignored (help)
  15. Dudley, A. T.; Lyons, K. M.; Robertson, E. J. (15 November 1995). "A requirement for bone morphogenetic protein-7 during development of the mammalian kidney and eye". Genes & Development. 9 (22): 2795–2807. doi: 10.1101/gad.9.22.2795 . ISSN   0890-9369. PMID   7590254.
  16. Dudley, A. T.; Robertson, E. J. (1997). "Overlapping expression domains of bone morphogenetic protein family members potentially account for limited tissue defects in BMP7 deficient embryos". Developmental Dynamics. 208 (3): 349–362. doi:10.1002/(SICI)1097-0177(199703)208:3<349::AID-AJA6>3.0.CO;2-I. ISSN   1058-8388. PMID   9056639. S2CID   32956921.
  17. Solloway, M. J.; Robertson, E. J. (1999). "Early embryonic lethality in Bmp5;Bmp7 double mutant mice suggests functional redundancy within the 60A subgroup". Development. 126 (8): 1753–1768. doi:10.1242/dev.126.8.1753. ISSN   0950-1991. PMID   10079236.
  18. Brennan, J.; Lu, C. C.; Norris, D. P.; Rodriguez, T. A.; Beddington, R. S.; Robertson, E. J. (21 June 2001). "Nodal signalling in the epiblast patterns the early mouse embryo". Nature. 411 (6840): 965–969. Bibcode:2001Natur.411..965B. doi:10.1038/35082103. ISSN   0028-0836. PMID   11418863. S2CID   4402639.
  19. Lu, Cindy C.; Robertson, Elizabeth J. (1 September 2004). "Multiple roles for Nodal in the epiblast of the mouse embryo in the establishment of anterior-posterior patterning". Developmental Biology. 273 (1): 149–159. doi: 10.1016/j.ydbio.2004.06.004 . ISSN   0012-1606. PMID   15302604.
  20. Brennan, Jane; Norris, Dominic P.; Robertson, Elizabeth J. (15 September 2002). "Nodal activity in the node governs left-right asymmetry". Genes & Development. 16 (18): 2339–2344. doi:10.1101/gad.1016202. ISSN   0890-9369. PMC   187443 . PMID   12231623.
  21. "Editors and Board". dev.biologists.org. Retrieved 2 March 2017.
  22. Developmental Biology Editorial Board . Retrieved 10 April 2018.{{cite book}}: |website= ignored (help)
  23. Current Opinion in Genetics & Development Editorial Board . Retrieved 10 April 2018.{{cite book}}: |website= ignored (help)
  24. "Developmental Cell Editorial Board" . Retrieved 2 March 2017.
  25. "No. 64269". The London Gazette (Supplement). 30 December 2023. p. N11.
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  27. Fellows of the Royal Society, RoyalSociety.org; accessed 9 April 2018.
  28. "EMBO Membership Pocket Guide" (PDF). Embo.org. Retrieved 10 April 2018.
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  30. British Society for Developmental Biology, bsdb.org; accessed 9 April 2018.
  31. 1 2 3 4 5 6 7 8 9 10 11 Hoffmann, Ilire Hasani, Robert. "Academy of Europe: Robertson Elizabeth". ae-info.org. Retrieved 2 March 2017.{{cite web}}: CS1 maint: multiple names: authors list (link)