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Molecular physiology of behavior

Molecular physiology of behavior

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Research

The interest of the laboratory combines neurobiology and physiology, along with -omics and behavioral approaches, to try to answer a basic question in neuroscience: how the brain processes and responds to environmental signals to coordinate innate and adaptive responses. Success in the response allows organisms to survive. This objective is addressed through three lines of research that use Drosophila melanogaster (the vinegar fly) as a model system.

Lines of investigation

Line 1.- Functions of the Drosophila PTTH/Torso neurohormonal axis in adult physiology

The neuroendocrine axis responsible for the juvenile-adult transition is likely already present in the ancestor of vertebrates and insects. In Drosophila the ptth gene (and its torso receptor) has functions equivalent to vertebrate GnRH (and its GnRHR receptor) during this transition. However, in both cases ptth and GnRH are expressed in the adult brain with functions not well described. Our objective is to study these functions in Drosophila, determining the cellular networks used by PTTH/Torso to regulate systemic physiological processes and the transcriptional profile in the target tissues of ptth mutant animals.

Fig 1.- Expression of ptth in the brain of the larva, in young flies recently emerged from the pupa and in aged animals.

Line 2.- Genomic bases of long-term memory

Long-term memory formation requires changes in transcriptional activity. Given the conservation of the molecular mechanisms of memory known up to now between the different species, we will use the fruit fly together with the genetic and -omics tools available to answer two questions about memory. On the one hand, to study whether social interaction causes a specific memory that causes changes in behavior. On the other, to determine the transcriptional changes during memory reactivation, functionally testing the most relevant candidate genes. The results obtained will allow us to know if there is a conserved pattern between types of memory or even between species.

Figure 2.- The learning paradigms used in the laboratory. A male, after unsuccessfully courting a female, when facing the stimulus (female) again decreases his courtship time. In a memory mutant the fly courts like the first time. In the social interaction test, we compare flies that have grown social (social interaction) with flies grown in solitude (isolation).

Line 3.- Effect of healthy aging on cognitive abilities

Given the increase in neurodegenerative diseases and cognitive problems that accompany an increasingly aging population, one of the objectives of our society is to maintain a better quality of life in old age. Moderate exercise has been shown to improve several physiological aspects altered by age. This line of research aims to establish Drosophila as a model to study at the molecular level the effect of exercise on brain function during aging. We are also interested in studying the functional consequences of altering PTTH levels during the decline caused by age, paying attention to gender differences. We hope that our results will allow us to explore new ways to counteract the effect of aging in humans.

Figure 3.- The apparatus used to exercise flies for 5 days. Subsequently, the animals are left to age for 25 days and it is tested how different cognitive and physiological aspects improve: learning, social interaction, sleep, resistance to stress and longevity.

Team

Francisco A. Martín Castro 

Principal Investigator

Maria del Carmen Rodriguez Navas

Laboratory technician

Esther Seco Martín

Laboratory technician

Celia González Barredo

Predoctoral researcher, UAM (FPI- UAM)

Beatriz Gil Martí

Predoctoral researcher, UAM (FPI- UAM)

Sara Piña Flores

Predoctoral researcher, UAM (FPU)

Julia Isidro Mezcua 

TFM student, UAM (JAE intro-CSIC)

Irene Camacho Agudo 

TFG student, UCM

Publications 

Publications

  • A simplified Courtship Conditioning protocol to test learning and memory in Drosophila. Gil-Marti B*, Barredo CG, Pina-Flores S, Poza-Rodriguez A, Treves G, Rodriguez-Navas C, Camacho L, Pérez-Serna A, Jimenez I, Brazales L, Fernandez J, Martín FA* (2023). STAR protocols 4:101572; DOI: 10.1016/j.xpro.2022.101572
  • Alignment between glioblastoma internal clock and environmental cues ameliorates survival in Drosophila. Jarabo P, Barredo CG, De Pablo C, Casas-Tinto S*, Martín FA* (2022). Communications Biology 5, 644; DOI: 10.1038/s42003-022-03600-9
  • The elusive transcriptional memory trace. Gil-Marti B, Barredo CG, Pina-Flores S, Trejo JL, Turiegano E, Martín FA* (2022). Oxford Open Neuroscience. Volume 1, kvac008; DOI: 10.1093/oons/kvac008.
  • Editorial: Behavior-Driven Changes in Gene Expression. Ferrus A*, Martín FA*, Tuesta LM*, Martín-Peña A* (2022) Frontiers in Behavioral Neuroscience 16:839395.
  • Barredo CG, Gil-Marti B, Deveci D, Romero NM*, Martín FA* (2021). Timing the juvenile-adult neurohormonal transition: functions and evolution. Frontiers in Endocrinology 11:602285
  • Insulin signaling mediates neurodegeneration in glioma. Jarabo P, De Pablo C, Herranz H, Martín FA*, Casas-Tinto S* (2021). Life Science Alliance 4 (3) e202000693; DOI: 10.26508/lsa.
  • Glioblastoma models in Drosophila melanogaster. Losada-Pérez M*, Jarabo P*, Martín FA*, Casas-Tintó S* (2020). In: eLS. John Wiley & Sons, Ltd:Chichester. DOI: 10.1002/9780470015902.a0022540.pub2
  • AstA signaling functions as an evolutionary conserved mechanism timing juvenile to adult transition. Deveci D, Martín FA, Leopold P, Romero NM (2019). Current Biology 29, 813-822. DOI 10.1016/j.cub.2019.01.053
  • Prothoracicotropic hormone modulates environmental adaptive plasticity through the control of developmental timing. Shimell MJ, Pan X, Martín FA, Ghosh AC, Leopold L, O’Connor MB, Romero NM (2018). Development 145: dev159699. DOI: 10.1242/dev.159699
  • Neurogenetics of Drosophila circadian clock: expect the unexpected. Jarabo P, Martín FA* (2017). Journal of Neurogenetics 4:1-16. DOI: 10.1080/01677063.2017.1370466
  • Ligand independent requirements of steroid receptors EcR and USP for cell survival. Mansilla A*, Martín FA*, Martín D, Ferrús A (2016). Cell Death and Differentiation 23:405-16. DOI: 10.1038/cdd.2015.108.

    Contact

    Where to find us

    Behavioral Molecular Physiology Group. Laboratory C-22

    Instituto Cajal CSIC. Avda. Doctor Arce, 37. 28002. Madrid

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    Phone number:

    +34 585 47 39

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    Email address:

    famartin@cajal.csic.es

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