Anne Ephrussi

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Anne Ephrussi (born 15 September 1955 in Paris, France) is a French developmental and molecular biologist. Her research is focused on the study of post-transcriptional regulations such as mRNA localization and translation control in molecular biology as well as the establishment of polarity axes in cell and developmental biology. [1] She is director of the EMBL International Centre for Advanced Training (EICAT) program at the European Molecular Biology Laboratory (EMBL) [2] [3] since 2005 and served as head of the Developmental Biology Unit from 2007 to 2021.

Contents

Biography

Anne Ephrussi studied biology at Harvard University in the Department of Biochemistry and Molecular Biology from where she graduated in 1979. She continued to do her PhD at the Massachusetts Institute of Technology (MIT) in the group of Susumu Tonegawa where she received her doctoral degree in 1985. Ephrussi performed postdoctoral research at Harvard University in the lab of Thomas Maniatis from 1986 to 1989 and at the Whitehead Institute for Biomedical Research with Ruth Lehmann from 1989 to 1992. Since 1992, Anne Ephrussi has been a group leader at the European Molecular Biology Laboratory (EMBL). She became the head of EMBL International Centre for Advanced Training in 2005. [2] [4] She served as Associate Dean (1999 - 2005) and Dean (2005 - 2008) of Graduate Studies of the EMBL International PhD program and as head of the developmental biology unit (2007-2021). She is part of numerous international Scientific Advisory Boards and Panels, organizes international conferences and scientific meetings and evaluates research grant and fellowship applications for a variety of renowned funding bodies.

Personal Details

Anne Ephrussi has French and American citizenship. She is the daughter of Boris Ephrussi and Harriett Ephrussi-Taylor. [5] She lives in Heidelberg, is married and has one child.

Research

With her research, Anne Ephrussi has contributed to the elucidation of the crucial role that spatial and temporal control of mRNA localization and translation play in oocyte development and cell polarity. [6]

Ephrussi established that oskar RNA is accumulated at and thereby defines the posterior pole of the Drosophila oocyte. [7] Aberrant localization and translation leads to germ cell formation defects and mispatterning during development. [8] Proper localization of oskar mRNA is ensured by concerted actions of the exon junction complex [9] [10] [11] and oskar's 3’ UTR [12] followed by a microtubule-based movement. During transport, translation of oskar is repressed by the RNA-binding protein Bruno, which is in turn released by the binding of activators (e.g. Orb) upon arrival at the posterior pole. [13] After proper localization, oskar RNA is translated and organizes germ plasm by recruiting other proteins such as Vasa. [14]

Her lab's current research continues to focus on spatial and temporal control of translation and which role ribonucleoprotein complexes (RNPs), cytoskeletal polarization and cytoskeletal motors play in RNA localization. Further, the roles of non-canonical RNA binding proteins in development as well as germ plasm assembly and function are investigated. These questions are tackled using a combination of genetics, biochemistry and a broad spectrum of cell bio logical and imaging approaches using the large Drosophila melanogaster oocyte as a model.

Honors and awards

Editorial Boards

Related Research Articles

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An oocyte, oöcyte, or ovocyte is a female gametocyte or germ cell involved in reproduction. In other words, it is an immature ovum, or egg cell. An oocyte is produced in a female fetus in the ovary during female gametogenesis. The female germ cells produce a primordial germ cell (PGC), which then undergoes mitosis, forming oogonia. During oogenesis, the oogonia become primary oocytes. An oocyte is a form of genetic material that can be collected for cryoconservation.

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oskar is a gene required for the development of the Drosophila embryo. It defines the posterior pole during early embryogenesis. Its two isoforms, short and long, play different roles in Drosophila embryonic development. oskar was named after the main character from the Günter Grass novel The Tin Drum, who refuses to grow up.

<span class="mw-page-title-main">Gurken localisation signal</span>

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Staufen is a protein product of a maternally expressed gene first identified in Drosophila melanogaster. The protein has been implicated in helping regulate genes important in determination of gradients that set up the anterior posterior axis such as bicoid and oskar. Staufen proteins, abbreviated Stau, are necessary for cell localization during the oogenesis and zygotic development. It is involved in targeting of the messenger RNA encoding these genes to the correct pole of the egg cell.

Vasa is an RNA binding protein with an ATP-dependent RNA helicase that is a member of the DEAD box family of proteins. The vasa gene is essential for germ cell development and was first identified in Drosophila melanogaster, but has since been found to be conserved in a variety of vertebrates and invertebrates including humans. The Vasa protein is found primarily in germ cells in embryos and adults, where it is involved in germ cell determination and function, as well as in multipotent stem cells, where its exact function is unknown.

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Ruth Lehmann is a developmental and cell biologist. She is the Director of the Whitehead Institute for Biomedical Research. She previously was affiliated with the New York University School of Medicine, where she was the Director of the Skirball Institute of Biomolecular Medicine, the Laura and Isaac Perlmutter Professor of Cell Biology, and the Chair of the Department of Cell Biology. Her research focuses on germ cells and embryogenesis.

Elisa Izaurralde was an Uruguayan biochemist and molecular biologist. She served as Director and Scientific Member of the Department of Biochemistry at the Max Planck Institute for Developmental Biology in Tübingen from 2005 until her death in 2018. In 2008, she was awarded the Gottfried Wilhelm Leibniz Prize, shared with Elena Conti, for "fundamental new insights into intracellular RNA transport and RNA metabolism". Together with Conti, she helped characterize proteins important for exporting mRNA out of the nucleus and later in her career she helped elucidate mechanisms of mRNA silencing, translational repression, and mRNA decay.

<span class="mw-page-title-main">Melina Schuh</span> German molecular biologist

Melina Schuh is a German biochemist and Director at the Max Planck Institute for Multidisciplinary Sciences. She is known for her work on meiosis in mammalian oocytes, for her studies on the mechanisms leading to the age-related decline in female fertility, and for the development of the Trim-Away protein depletion method.

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References

  1. "Ephrussi Group – RNA localisation and localised translation in development" . Retrieved 7 September 2022.
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  6. Besse, Florence; Ephrussi, Anne (2008). "Translational control of localized mRNAs: restricting protein synthesis in space and time". Nature Reviews Molecular Cell Biology. 9 (12): 971–980. doi:10.1038/nrm2548. ISSN   1471-0072. PMID   19023284. S2CID   35745917.
  7. Ephrussi, Anne; Dickinson, Laura K.; Lehmann, Ruth (1991). "oskar organizes the germ plasm and directs localization of the posterior determinant nanos". Cell. 66 (1): 37–50. doi:10.1016/0092-8674(91)90137-N. PMID   2070417. S2CID   23006074.
  8. Ephrussi, Anne; Lehmann, Ruth (1992). "Induction of germ cell formation by oskar". Nature. 358 (6385): 387–392. Bibcode:1992Natur.358..387E. doi:10.1038/358387a0. ISSN   0028-0836. PMID   1641021. S2CID   4269753.
  9. Markussen, F. H.; Michon, A. M.; Breitwieser, W.; Ephrussi, A. (1995). "Translational control of oskar generates short OSK, the isoform that induces pole plasma assembly". Development. 121 (11): 3723–3732. doi:10.1242/dev.121.11.3723. ISSN   0950-1991. PMID   8582284.
  10. Hachet, Olivier; Ephrussi, Anne (2004). "Splicing of oskar RNA in the nucleus is coupled to its cytoplasmic localization". Nature. 428 (6986): 959–963. Bibcode:2004Natur.428..959H. doi:10.1038/nature02521. ISSN   0028-0836. PMID   15118729. S2CID   4413199.
  11. Ghosh, Sanjay; Marchand, Virginie; Gáspár, Imre; Ephrussi, Anne (2012). "Control of RNP motility and localization by a splicing-dependent structure in oskar mRNA". Nature Structural & Molecular Biology. 19 (4): 441–449. doi:10.1038/nsmb.2257. ISSN   1545-9993. PMID   22426546. S2CID   20099525.
  12. Jambor, Helena; Mueller, Sandra; Bullock, Simon L.; Ephrussi, Anne (2014). "A stem-loop structure directs oskar mRNA to microtubule minus ends". RNA. 20 (4): 429–439. doi:10.1261/rna.041566.113. ISSN   1469-9001. PMC   3964905 . PMID   24572808.
  13. Chekulaeva, Marina; Hentze, Matthias W.; Ephrussi, Anne (2006). "Bruno Acts as a Dual Repressor of oskar Translation, Promoting mRNA Oligomerization and Formation of Silencing Particles". Cell. 124 (3): 521–533. doi: 10.1016/j.cell.2006.01.031 . PMID   16469699. S2CID   6308889.
  14. Breitwieser, W; Markussen, F H; Horstmann, H; Ephrussi, A (1996). "Oskar protein interaction with Vasa represents an essential step in polar granule assembly". Genes & Development. 10 (17): 2179–2188. doi: 10.1101/gad.10.17.2179 . ISSN   0890-9369. PMID   8804312.
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  24. Earnshaw, William C.; Ephrussi, Anne (1997). "New faces for the new year". Trends in Cell Biology. 7 (1): 38–39. doi:10.1016/S0962-8924(97)89929-1. PMID   17708897.
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