Jordi Casanova

ORCID: 0000-0001-6121-8589
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About
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Research Areas
  • Developmental Biology and Gene Regulation
  • Neurobiology and Insect Physiology Research
  • Invertebrate Immune Response Mechanisms
  • Hippo pathway signaling and YAP/TAZ
  • Wnt/β-catenin signaling in development and cancer
  • Plant Molecular Biology Research
  • RNA Research and Splicing
  • Genomics and Chromatin Dynamics
  • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
  • Protist diversity and phylogeny
  • Cellular Mechanics and Interactions
  • Chromosomal and Genetic Variations
  • Epigenetics and DNA Methylation
  • Studies on Chitinases and Chitosanases
  • Microtubule and mitosis dynamics
  • Animal Genetics and Reproduction
  • Insect Resistance and Genetics
  • Silk-based biomaterials and applications
  • Cancer Cells and Metastasis
  • Congenital heart defects research
  • Marine Ecology and Invasive Species
  • Genetics, Aging, and Longevity in Model Organisms
  • Cell Adhesion Molecules Research
  • Viral Infectious Diseases and Gene Expression in Insects
  • Proteoglycans and glycosaminoglycans research

Institute for Research in Biomedicine
2015-2025

Institut de Biologia Molecular de Barcelona
2015-2025

Institute for Research in Biomedicine
2014-2023

Universitat de Barcelona
2007-2018

Consejo Superior de Investigaciones Científicas
1995-2010

University Children’s Hospital Basel
2008

Hôpital Necker-Enfants Malades
2008

Human Genetic of Infectious Diseases
2008

Pediatrics and Genetics
2008

Centro de Biología Molecular Severo Ochoa
1985-2007

Differentiation of the embryonic termini in Drosophila depends on signaling by Tor RTK, which induces terminal gene expression inactivating at poles a uniformly distributed repressor activity that involves Gro corepressor. Here, we identify new gene, cic , acts as genes regulated pathway. also mediates repression along dorsoventral axis, process requires Dorsal morphogen and Gro, is inhibited termini. encodes an HMG-box transcription factor interacts with vitro. We present evidence regulates...

10.1101/gad.14.2.224 article EN Genes & Development 2000-01-15

The subdivision of the Drosophila body into distinct terminal and central domains depends on torso (tor) protein, a putative receptor tyrosine kinase that is active at both ends early embryo. We show tor protein uniformly expressed along surface membrane embryos despite its localized activity poles. Further, we present evidence polarized this other gene functions, one which may be extracellular ligand generated during oogenesis. Finally, using temperature-sensitive gain-of-function mutation...

10.1101/gad.3.12b.2025 article EN Genes & Development 1989-12-01

Metastasis underlies the majority of cancer-related deaths yet remains poorly understood due, in part, to lack models vivo. Here we show that expression EMT master inducer Snail primary adult Drosophila intestinal tumors leads dissemination tumor cells and formation macrometastases. drives an cells, which, although retaining some epithelial markers, subsequently break through basal lamina midgut, undergo a collective migration seed polyclonal metastases. While metastases re-epithelialize...

10.1038/s41467-019-10269-y article EN cc-by Nature Communications 2019-05-24

By using a hsp70-Ubx fusion gene, we have ectopically expressed Ubx product in the embryonic head primordia and studied developmental effects on larval head. We find that after high persistent levels of product, is replaced by three (C1, C2 C3) abdominal-like denticle belts. The C3 belts are homeotic transformations parasegments 1 2, respectively, while C1 belt probably derives from transformation subsequent most anterior procephalic primordia. On basis their response to other arguments,...

10.1242/dev.113.4.1459 article EN PubMed 1991-12-01

10.1016/j.cub.2009.12.043 article EN publisher-specific-oa Current Biology 2010-02-01

Body size in holometabolous insects is determined by the at which juvenile larva undergoes metamorphosis to pupal stage. To undergo larva-pupa transition, must reach a critical developmental checkpoint, threshold (TS); however, molecular mechanisms through TS cues this transition remain be fully characterized. Here, we use flour beetle Tribolium castaneum characterize underlying entry into metamorphosis. We found that T. reaches beginning of last larval instar, associated with downregulation...

10.1016/j.celrep.2019.03.094 article EN cc-by-nc-nd Cell Reports 2019-04-01

The extracellular matrix (ECM), a structure contributed to and commonly shared by many cells in an organism, plays active role during morphogenesis. Here, we used the Drosophila tracheal system study complex relationship between ECM epithelial development. We show that there is feedback mechanism apical (aECM) F-actin cells. Furthermore, reveal cell-cell junctions are key players this aECM patterning organisation individual contribute autonomously their aECM. Strikingly, changes influence...

10.7554/elife.09373 article EN cc-by eLife 2016-02-02

Organ morphogenesis requires the coordinated activity of many mechanisms involved in cell rearrangements, size control, proliferation and organ integrity. Here we report that Lachesin (Lac), a surface protein, is required for proper Drosophila tracheal system. Homozygous embryos Lac mutations, which find fail to complement previous identified bulbous (bulb) mutation, display convoluted tubes tube breaks. At cellular level, can detect enlarged cells, suggesting regulates by influencing length...

10.1242/dev.00917 article EN Development 2003-12-17

The ventral veinless gene (vvl) encodes the previously identified Cf1a protein, a transcription factor containing POU-domain. During embryonic development vvl function is required for formation of tracheal tree and in patterning ectoderm. imaginal cell proliferation differentiation wing veins. expression restricted to regions where its required, dependent on coordinate activities signalling molecules such as decapentaplegic, wingless hedgehog. interacts with other genes involved vein...

10.1242/dev.121.10.3405 article EN Development 1995-10-01

The specification of the most anterior and posterior domains Drosophila embryo depends on activity torso protein, a putative tyrosine kinase receptor. Localized at poles generates graded information that specifies distinct portions body. primary response to terminal signal in end is likely be activation gap genes huckebein tailless. Here I address question how maternal different elements pattern what role tailless activities may play this process. These experiments show distinctly localized...

10.1242/dev.110.2.621 article EN Development 1990-10-01

A major issue in morphogenesis is to understand how the activity of genes specifying cell fate affects cytoskeletal components that modify shape and induce movements. Here, we approach this question by investigating a group cells from an epithelial sheet initiate invagination ultimately form Drosophila tracheal tubes. We describe behavior at show it associated with, requires, distinct recruitment Myosin II apical surface invaginating edge. process achieved crossveinless-c , gene coding for...

10.1101/gad.375706 article EN Genes & Development 2006-07-01

The transcriptional repressor Capicua (Cic) controls multiple aspects of Drosophila embryogenesis and has been implicated in vertebrate development human diseases. Receptor tyrosine kinases (RTKs) can antagonize Cic-dependent gene repression, but the mechanisms responsible for this effect are not fully understood. Based on genetic imaging studies early embryo, we found that Torso RTK signaling increase rate Cic degradation by changing its subcellular localization. We propose is degraded...

10.1242/dev.084327 article EN Development 2012-10-09

Whereas the series of genetic events leading to colorectal cancer (CRC) have been well established, precise functions that these alterations play in tumor progression and how they disrupt intestinal homeostasis remain poorly characterized. Activation Wnt/Wg signaling pathway by a mutation gene APC is most common trigger for CRC, inducing benign lesions progress carcinomas due accumulation other alterations. Among those, Ras mutations drive tumour as epithelial cancers. As mammalian...

10.1371/journal.pone.0088413 article EN cc-by PLoS ONE 2014-02-06
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