Michel Delseny

Last updated

Michel Delseny (born June 17, 1945) is director of research emeritus at the CNRS and a member of the French Academy of sciences.

Contents

Delseny initially focused on the study of gene expression in higher plants, mainly during seed development and germination, as well as in response to stress. He later contributed to the development of plant genomics and focused on the organization and evolution of plant genomes.

Biography

University degrees

After a Baccalaureate C in Paris in 1963, he obtained a master's degree in natural sciences: Plant Biology and Physiology in Paris in 1968, then a diploma of advanced studies: plant cytology and morphogenesis in Paris in 1969. He passed the agrégation and CAPES in Natural Sciences (1st in both competitions) in 1970, then obtained a doctorate in biochemistry in Montpellier in 1972 and a doctorate in molecular biology in Montpellier in 1977.

Positions held

Administrative responsibilities

Delseny was an elected member of the CNRS National Committee for 3 terms of 4 years. He was appointed member of the Institut national de la recherche agronomique (INRA) scientific commissions for 2 terms of 4 years, member of the MICAP scientific council, Mission à la connaissance et à l'amélioration des plantes (CIRAD) for 2 terms, member of the scientific council of the École nationale supérieure d'agronomie de Montpellier from 2002 until the end of 2006, member of the Board of Directors of the ISPMB (International Society for Plant Molecular Biology) from 1998 to 2002 and co-organizer, with Père Puigdomenech, of the ISPMB International Congress in Barcelona in June 2003 and member of the operational board of Génoplante from 1999 to 2004. He is a member of the Environmental Sciences Committee, the Science and Biosafety Committee of the French Academy ofsSciences, the Working Group on Artificial Intelligence and a member of the management board of the Foundation of the University of Perpignan Via Domitia (UPVD) since 2014.

He was co-responsible, with Claude Gigot (IBMC Strasbourg) for the RCP (Cooperative Research on Programme) of the CNRS "Isolation, structure and expression of the nuclear genome of plants" and coordinator of the European EuDicotMap project between 1997 and 2000.

Delseny was also associate editor of Plant Molecular Biology (1996-2006), Plant Cell Physiology (4 years, from 2009 to 2013, then the advisory editorial board until 2017), and Botanical Studies since 2014, co-editor in chief of Plant Science from 2003 to 2015, co-editor in chief of Advance in Botanical Research, from 2006 to 2014, co-editor of CR Biologies (2018-).

He is deputy director of Génopole Montpellier Languedoc-Roussillon (1999-2006), president of CSD 7 (Ecological Agronomy) of the ANR's White Programme (2005-2007), vice-president of COPED (Developing Countries Committee) of the French Academy of sciences (2017-2021).

Finally, he has been the referent of the pilot centre of La Main à la pâte of Perpignan [2] since 2014 and of the Maison pour la Science de Toulouse since 2017 [3] and a member of the scientific council of La Main à la pâte. [4]

Teaching activities

Throughout his career, Delseny has been involved in teaching activities, most often on a voluntary basis at the University of Perpignan. Following Yves Guitton's death in July 1977, he taught biochemistry and plant physiology with his colleague Françoise Grellet in DEUG and master's degree from September 1978 to June 1979, pending the appointment of his replacement, Paul Penon.

Delseny has participated in postgraduate teaching in a significant way: in charge of the "development biology" module of the DEA and then of the master's degree in Montpellier since 1996, until 2007. He was Director of the ED 305 Doctoral School "Biologie environnement sciences pour l'ingénieur" in Perpignan from 2003 to 2006 and a member of the Board of the SIBAGH Doctoral School in Montpellier from 1996 to 2009.  He has been a member of the Scientific Council of ED 305 since 2015.

Delseny has participated or organized advanced practical or theoretical courses abroad or in France: Valdivia (Chile), Mar del Plata (Argentina), Bordeaux, Perpignan, Pau, Montpellier, Barcelona, Cabrils (Spain), Hsinchu, Taipei and Tainan (Taiwan).

He has directed, or co-directed, the work of 30 thesis students, as many post-doctoral fellows and foreign visitors and participated in 9 thèses d'État juries, 135 university theses and 25 research authorizations.

Publications

About 200 publications in peer-reviewed journals (Plant Physiology, Plant Journal, Plant Cell, Nature, Planta, European Journal of Biochemistry, FEBS Letters, EMBO J, PNAS, Plant Physiology and Biochemistry, Plant Science...) and numerous popular articles and book chapters (H index 46). [5]

He has participated in 3 patents and has been a guest speaker at hundreds of national and international conferences and has given about 200 seminars, in France and abroad.

Research

Michel Delseny was one of the first scientists to characterize plant RNA messengers in 1974. [6]

He was among the first to show (during his post-doctoral fellowship in 1979–1980) that the Cauliflower Mosaic Virus (CaMV) DNA, after cloning and amplification in Escherichia coli, was infectious and identical to the original DNA when inoculated to a host plant. [7]

He was among the first in France to clone and sequence plant DNA in the early 1980s, [7] [8] [9] and, as such, he helped to organize the community of plant biology researchers in France by creating in 1984 with Claude Gigot (IBMC Strasbourg) the CNRS's RCP (Recherche Coopérative sur Programme) "Isolation, structure et expression du génome nucléaire des plantes" which is at the origin of the development of plant molecular biology in France.

He was the first to report the sequence of the spacer of genes encoding ribosomal RNAs of a dicotyledon in 1988 and to show the bases of ribosomal gene heterogeneity in plants. [8] [10] These observations had a strong impact, as it was the beginning of collaborations with the plant breeding sector at INRA, IRD, CIRAD and with private partners. From there, they developed molecular tools that are still widely used, including microsatellites and RAPDs. The 1990s were marked by their participation in major sequencing programs for Arabidopsis genomes [11] [12] [13] and rice [14] [15] and thus discovered many genes whose function they elucidated. They also discovered in 2000 that plant genomes had undergone global duplication cycles during the evolution of cycles [13] and thus contributed to the current conception of genome evolution. [16] They also characterized the first cassava cDNAs [17] and participated in the sequencing of the unicellular alga Ostreococcus tauri. [18]

Among the genes characterized and discovered in his laboratory are the genes of radish reserve proteins since 1985, the genes of LEA (Late Embryogenesis Abundant) proteins and their regulation, proteins omnipresent in seeds, whose function is undoubtedly to facilitate the survival of the seed during its dehydration, [19] [20] the first gene of a lipid transfer protein in 1988 with Jean-Claude Kader and Père Puigdomenech, then other members of this family involved in the defense against pathogenic fung i, [21] several genes essential for the proper development of embryogenesis, [22] the ABI 5 regulatory gene involved in regulating maturation and seed germination in 2001, [23] several genes involved in controlling ribosomal RNA formation (fibrillarine, nucleolin, snoRNA) and ribosomes that synthesize proteins, several genes involved in lipid biosynthesis in rapeseed, and, recently, one of the genes responsible for the aroma of Basmati rice, [24] as well as the first gene regulating cell death in plants [25] ...

Following the discovery by his collaborators of genes encoding small regulatory RNAs (miRNA and siRNA) and for new RNA polymerases, his laboratory is now involved in epigenetics and the control of gene expression by small RNAs. The development of genomics continues there under the leadership of Olivier Panaud.

Awards [26]

Related Research Articles

<i>Arabidopsis</i> Genus of flowering plants

Arabidopsis (rockcress) is a genus in the family Brassicaceae. They are small flowering plants related to cabbage and mustard. This genus is of great interest since it contains thale cress, one of the model organisms used for studying plant biology and the first plant to have its entire genome sequenced. Changes in thale cress are easily observed, making it a very useful model.

<i>Arabidopsis thaliana</i> Model plant species in the family Brassicaceae

Arabidopsis thaliana, the thale cress, mouse-ear cress or arabidopsis, is a small flowering plant native to Eurasia and Africa. A. thaliana is considered a weed; it is found along the shoulders of roads and in disturbed land.

<span class="mw-page-title-main">Transfer DNA</span>

The transfer DNA is the transferred DNA of the tumor-inducing (Ti) plasmid of some species of bacteria such as Agrobacterium tumefaciens and Agrobacterium rhizogenes(actually an Ri plasmid). The T-DNA is transferred from bacterium into the host plant's nuclear DNA genome. The capability of this specialized tumor-inducing (Ti) plasmid is attributed to two essential regions required for DNA transfer to the host cell. The T-DNA is bordered by 25-base-pair repeats on each end. Transfer is initiated at the right border and terminated at the left border and requires the vir genes of the Ti plasmid.

Florigen is the hypothesized hormone-like molecule responsible for controlling and/or triggering flowering in plants. Florigen is produced in the leaves, and acts in the shoot apical meristem of buds and growing tips. It is known to be graft-transmissible, and even functions between species. Florigen has been found identical to the transcription factor FLOWERING LOCUS T (FT).

<span class="mw-page-title-main">Small nucleolar RNA SNORD15</span>

In molecular biology, SNORD15 is a non-coding RNA (ncRNA) molecule which functions in the modification of other small nuclear RNAs (snRNAs). This type of modifying RNA is usually located in the nucleolus of the eukaryotic cell which is a major site of snRNA biogenesis. It is known as a small nucleolar RNA (snoRNA) and also often referred to as a guide RNA.

<span class="mw-page-title-main">Small nucleolar RNA SNORD43</span>

In molecular biology, snoRNA U43 is a non-coding RNA (ncRNA) molecule which functions in the modification of other small nuclear RNAs (snRNAs). This type of modifying RNA is usually located in the nucleolus of the eukaryotic cell which is a major site of snRNA biogenesis. It is known as a small nucleolar RNA (snoRNA) and also often referred to as a guide RNA.

Evolutionary developmental biology (evo-devo) is the study of developmental programs and patterns from an evolutionary perspective. It seeks to understand the various influences shaping the form and nature of life on the planet. Evo-devo arose as a separate branch of science rather recently. An early sign of this occurred in 1999.

<span class="mw-page-title-main">Plant evolution</span> Subset of evolutionary phenomena that concern plants

Plant evolution is the subset of evolutionary phenomena that concern plants. Evolutionary phenomena are characteristics of populations that are described by averages, medians, distributions, and other statistical methods. This distinguishes plant evolution from plant development, a branch of developmental biology which concerns the changes that individuals go through in their lives. The study of plant evolution attempts to explain how the present diversity of plants arose over geologic time. It includes the study of genetic change and the consequent variation that often results in speciation, one of the most important types of radiation into taxonomic groups called clades. A description of radiation is called a phylogeny and is often represented by type of diagram called a phylogenetic tree.

<span class="mw-page-title-main">LTR retrotransposon</span> Class I transposable element

LTR retrotransposons are class I transposable element characterized by the presence of long terminal repeats (LTRs) directly flanking an internal coding region. As retrotransposons, they mobilize through reverse transcription of their mRNA and integration of the newly created cDNA into another location. Their mechanism of retrotransposition is shared with retroviruses, with the difference that most LTR-retrotransposons do not form infectious particles that leave the cells and therefore only replicate inside their genome of origin. Those that do (occasionally) form virus-like particles are classified under Ortervirales.

<span class="mw-page-title-main">Chloroplast DNA</span> DNA located in cellular organelles called chloroplasts

Chloroplast DNA (cpDNA) is the DNA located in chloroplasts, which are photosynthetic organelles located within the cells of some eukaryotic organisms. Chloroplasts, like other types of plastid, contain a genome separate from that in the cell nucleus. The existence of chloroplast DNA was identified biochemically in 1959, and confirmed by electron microscopy in 1962. The discoveries that the chloroplast contains ribosomes and performs protein synthesis revealed that the chloroplast is genetically semi-autonomous. The first complete chloroplast genome sequences were published in 1986, Nicotiana tabacum (tobacco) by Sugiura and colleagues and Marchantia polymorpha (liverwort) by Ozeki et al. Since then, a great number of chloroplast DNAs from various species have been sequenced.

Elizabeth Salisbury Dennis is an Australian scientist working mainly in the area of plant molecular biology. She is currently a chief scientist at the plant division of CSIRO Canberra. She was elected a Fellow of the Australian Academy of Technological Sciences and Engineering (FTSE) in 1987, and the Australian Academy of Science in 1995. She jointly received the inaugural Prime Minister's Science Prize together with Professor Jim Peacock in 2000 for her outstanding achievements in science and technology.

WRKY transcription factors are proteins that bind DNA. They are transcription factors that regulate many processes in plants and algae (Viridiplantae), such as the responses to biotic and abiotic stresses, senescence, seed dormancy and seed germination and some developmental processes but also contribute to secondary metabolism.

Circadian Clock Associated 1 (CCA1) is a gene that is central to the circadian oscillator of angiosperms. It was first identified in Arabidopsis thaliana in 1993. CCA1 interacts with LHY and TOC1 to form the core of the oscillator system. CCA1 expression peaks at dawn. Loss of CCA1 function leads to a shortened period in the expression of many other genes.

<span class="mw-page-title-main">Klaus Scherrer</span> French biologist of Swiss nationality (born 1931)

Klaus Scherrer is a French biologist of Swiss nationality. He is emeritus research director for the CNRS, member of EMBO, member of the academia Europaea and the Brazilian academy of sciences. He is Professor honoris causa of University of Brasilia.

LUX or Phytoclock1 (PCL1) is a gene that codes for LUX ARRHYTHMO, a protein necessary for circadian rhythms in Arabidopsis thaliana. LUX protein associates with Early Flowering 3 (ELF3) and Early Flowering 4 (ELF4) to form the Evening Complex (EC), a core component of the Arabidopsis repressilator model of the plant circadian clock. The LUX protein functions as a transcription factor that negatively regulates Pseudo-Response Regulator 9 (PRR9), a core gene of the Midday Complex, another component of the Arabidopsis repressilator model. LUX is also associated with circadian control of hypocotyl growth factor genes PHYTOCHROME INTERACTING FACTOR 4 (PIF4) and PHYTOCHROME INTERACTING FACTOR 5 (PIF5).

Arabidopsis thaliana is a first class model organism and the single most important species for fundamental research in plant molecular genetics.

<span class="mw-page-title-main">Micropeptide</span> Short length polypeptides

Micropeptides are polypeptides with a length of less than 100-150 amino acids that are encoded by short open reading frames (sORFs). In this respect, they differ from many other active small polypeptides, which are produced through the posttranslational cleavage of larger polypeptides. In terms of size, micropeptides are considerably shorter than "canonical" proteins, which have an average length of 330 and 449 amino acids in prokaryotes and eukaryotes, respectively. Micropeptides are sometimes named according to their genomic location. For example, the translated product of an upstream open reading frame (uORF) might be called a uORF-encoded peptide (uPEP). Micropeptides lack an N-terminal signaling sequences, suggesting that they are likely to be localized to the cytoplasm. However, some micropeptides have been found in other cell compartments, as indicated by the existence of transmembrane micropeptides. They are found in both prokaryotes and eukaryotes. The sORFs from which micropeptides are translated can be encoded in 5' UTRs, small genes, or polycistronic mRNAs. Some micropeptide-coding genes were originally mis-annotated as long non-coding RNAs (lncRNAs).

Jian-Kang Zhu is a plant scientist, researcher and academic. He is a Senior Principal Investigator in the Shanghai Center for Plant Stress Biology, Chinese Academy of Sciences (CAS). He is also the Academic Director of CAS Center of Excellence in Plant Sciences.

<span class="mw-page-title-main">RNA-directed DNA methylation</span> RNA-based gene silencing process

RNA-directed DNA methylation (RdDM) is a biological process in which non-coding RNA molecules direct the addition of DNA methylation to specific DNA sequences. The RdDM pathway is unique to plants, although other mechanisms of RNA-directed chromatin modification have also been described in fungi and animals. To date, the RdDM pathway is best characterized within angiosperms, and particularly within the model plant Arabidopsis thaliana. However, conserved RdDM pathway components and associated small RNAs (sRNAs) have also been found in other groups of plants, such as gymnosperms and ferns. The RdDM pathway closely resembles other sRNA pathways, particularly the highly conserved RNAi pathway found in fungi, plants, and animals. Both the RdDM and RNAi pathways produce sRNAs and involve conserved Argonaute, Dicer and RNA-dependent RNA polymerase proteins.

<span class="mw-page-title-main">Wojciech Karlowski</span> Polish biologist specializing in molecular biology and bioinformatics

Wojciech Maciej Karlowski is a Polish biologist specializing in molecular biology and bioinformatics, and a full professor in biological sciences. He is Head of the Department of Computational Biology at the Faculty of Biology at the Adam Mickiewicz University in Poznan. His major scientific interests include identification of non-coding RNAs, genomics, high-throughput analyses, and functional annotation of biological sequences.

References

  1. "Linkedin".
  2. "Centre Pilote La Main à la pâte de Perpigan".
  3. "Maison pour la sciences Toulouse".
  4. "La Main à la pâte".
  5. "Google Scholar".
  6. M.Delseny et al., « Détection de séquences polyriboadényliques dans les ARN de Radis », C.R. Acad. Sci., Série D, (1974), 278, p. 1225-1228
  7. 1 2 M. Delseny and R. Hull, « Isolation and characterization of faithful and altered clones of the genomes of cauliflower mosaic virus isolates Cabb B-JI, CM4-184, and Bari I », Plasmid, (1983), 9, p. 31-41
  8. 1 2 M. Delseny et al., « Sequences heterogeneity in radish nuclear ribosomal RNA genes », Plant Sci. Letters, (1983), 30, p. 107-111
  9. F. Grellet et al., « Organization and evolution of a higher plant alphoïd like satellite DNA sequence », J. Mol. Biol., (1986), 187, p. 495-507
  10. D. Delcasso-Tremousaygue et al., « Structural and transcriptional characterization of the external spacer of a ribosomal RNA nuclear gene from a higher plant », Eur. J. Biochem., (1988), 172, p. 767-776
  11. R. Cooke et al., « Further progress towards a catalogue of all Arabidopsis genes : analysis of a set of 5000 non-redundant ESTs », Plant J., (1996), 9, p. 101-124
  12. Salanoubat et al., « Sequence and analysis of chromosome 3 of the plant Arabidopsis thaliana », Nature, (2000), 408, p. 820-822
  13. 1 2 G. Blanc et al., « Extensive duplication and reshuffling in the Arabidopsis thaliana genome », Plant Cell, (2000), 12, p. 1093-11
  14. M. Delseny, « Towards an accurate sequence of the rice genome », Current Opinion in Plant Biol., (2003), 6, p. 101-105
  15. J. Sallaud et al., « High Throughput T-DNA Insertion Mutagenesis in Rice : A First Step towards in silico Reverse Genetics », Plant J., (2004), 39, p. 450-464
  16. J. Salse et al., « Identification and characterization of shared duplications between rice and wheat provide new insight into grass genome evolution », Plant Cell, (2008), 20, p. 11-24
  17. C. Lopez et al., « A unigene catalogue of 5700 expressed genes in Cassava (Manihot esculenta) », Plant Mol Biol, (2004), 56, p. 541-554
  18. E. Derelle et al., « Genome analysis of the smallest free-living eukaryote Ostreococcus tauri unveils many unique features », Proc Natl Acad Sc USA, (2006), 103, p. 11647-11652
  19. F. Parcy et al., « Regulation of gene expression programs during Arabidopsis seed development : roles of the ABI3 locus and of endogenous abscisic acid », The Plant Cell, (1994), 6, p. 1567-1582
  20. N. Bies-Etheve et al., « Inventory, evolution and expression profiling diversity of the LEA (Late Embryogenesis Abundant) protein gene family in Arabidopsis thaliana », Plant Mol Biol, (2008), 67, p. 107-112
  21. L. Sossountzov et al., « Spatial and temporal expression of a maize lipid transfer protein gene », The Plant Cell, (1991), 3, p. 923-933
  22. A. Ronceret et al., « Genetic analysis of two Arabidopsis DNA polymerase epsilon subunits during early embryogenesis », Plant J, (2005), 44, p. 223-236
  23. C .Carles et al., « Regulation of Arabidopsis thaliana Em genes: role of ABI5 », Plant J, (2002), 30, p. 1-13
  24. F. Bourgis et al., « Characterization of the major fragrance gene from an aromatic japonica rice and analysis of its diversity in Asian cultivated rice », Theor Appl Genet, (2008), 117, p. 353-368
  25. R. Blanvillain et al., « The Arabidopsis peptide KISS OF DEATH is an inducer of Programmed Cell Death », EMBO J, (2011), 30, p. 1173-1183
  26. 1 2 "Biographie Michel Delseny" (PDF). academie-sciences.fr.
  27. 1 2 "Journal officiel".