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- Challenges and Chances: A Review of the 1st Stem Cell Community Day
- Summertime, and the Livin’ Is Easy…
- Follow-on-Biologics – More than Simple Generics
- Bacteria Versus Body Cells: A 1:1 Tie
- Behind the Crime Scene: How Biological Traces Can Help to Convict Offenders
- Every 3 Seconds Someone in the World Is Affected by Alzheimer's
- HIV – It’s Still Not Under Control…
- How Many Will Be Convicted This Time?
- Malaria – the Battle is Not Lost
- Physicians on Standby: The Annual Flu Season Can Be Serious
- At the Forefront in Fighting Cancer
- Molecular Motors: Think Small and yet Smaller Again…
- Liquid Biopsy: Novel Methods May Ease Cancer Detection and Therapy
- They Are Invisible, Sneaky and Disgusting – But Today It’s Their Special Day!
- How Many Cells Are in Your Body? Probably More Than You Think!
- What You Need to Know about Antibiotic Resistance – Findings, Facts and Good Intentions
- Why Do Old Men Have Big Ears?
- The Condemned Live Longer: A Potential Paradigm Shift in Genetics
- From Research to Commerce
- Chronobiology – How the Cold Seasons Influence Our Biorhythms
- Taskforce Microbots: Targeted Treatment from Inside the Body
- Eyes on Cancer Therapy
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- 2022 Award Finalist Dr. Arnau Sebé-Pedrós
2022 Award Finalist Arnau Sebé-Pedrós, Ph.D.
I did my PhD (2009-2014) under the supervision of Iñaki Ruiz-Trillo at the University of Barcelona (Spain), investigating the origin of animal multicellularity from a comparative and functional genomics perspective. Then, I spent four years (2015-2018) at the Weizmann Institute of Science (Israel), working with Amos Tanay on single-cell analysis of animal cell type diversity and genomic regulation. Since 2019, I am a Group Leader at the CRG, within the Systems Biology program, where my group investigates the origin and evolution of cell type programs and associated genome regulatory novelties (transcription factors, enhancer elements, chromatin architecture).
Synopsis of research:
I am an evolutionary biologist interested in how genome sequence and its regulation translate into specific cellular phenotypes and, in particular, how this genotype-cell phenotype link evolves.
Cell types are the basic functional units of multicellular organisms. Distinct cell type transcriptional programs are deployed by regulatory mechanisms that control the differential access to genetic information in each cell. This genome regulation ultimately results in specific cellular phenotypes. However, the origin, diversity, and evolution of cell types and genome regulation remain largely unexplored. What are the regulatory mechanisms linked to the origin of cell differentiation? When did major animal cell types such as neurons emerge and did they evolve more than once? How do animal cell type gene regulatory networks evolve? And how these genetic changes translate into cellular novelties?
To answer these and related questions, in my group we combine chromatin profiling, proteomics, and single-cell technologies with computational genomics in order to dissect and compare cell type programs and genome regulatory architectures in phylogenetically diverse systems. This study has two major potential impacts. First, by systematically characterizing cell type diversity we advance our understanding of organismal evolution, function, and adaptation. Beyond that, the comparative study of these animal cell type programs can offer transformative insights linking classical models of molecular evolution with an intermediate molecular phenotype: cell type gene regulatory networks. Second, by studying genome function in non-traditional model species we can reveal fundamental, shared principles that govern cell biological systems and the associated molecular mechanisms of genome regulation.
Synopsis of research:
I am an evolutionary biologist interested in how genome sequence and its regulation translate into specific cellular phenotypes and, in particular, how this genotype-cell phenotype link evolves.
Cell types are the basic functional units of multicellular organisms. Distinct cell type transcriptional programs are deployed by regulatory mechanisms that control the differential access to genetic information in each cell. This genome regulation ultimately results in specific cellular phenotypes. However, the origin, diversity, and evolution of cell types and genome regulation remain largely unexplored. What are the regulatory mechanisms linked to the origin of cell differentiation? When did major animal cell types such as neurons emerge and did they evolve more than once? How do animal cell type gene regulatory networks evolve? And how these genetic changes translate into cellular novelties?
To answer these and related questions, in my group we combine chromatin profiling, proteomics, and single-cell technologies with computational genomics in order to dissect and compare cell type programs and genome regulatory architectures in phylogenetically diverse systems. This study has two major potential impacts. First, by systematically characterizing cell type diversity we advance our understanding of organismal evolution, function, and adaptation. Beyond that, the comparative study of these animal cell type programs can offer transformative insights linking classical models of molecular evolution with an intermediate molecular phenotype: cell type gene regulatory networks. Second, by studying genome function in non-traditional model species we can reveal fundamental, shared principles that govern cell biological systems and the associated molecular mechanisms of genome regulation.
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