4.0 Article

Continuous tracking of startled Drosophila as an alternative to the negative geotaxis climbing assay

Journal

JOURNAL OF NEUROGENETICS
Volume 33, Issue 3, Pages 190-198

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/01677063.2019.1634065

Keywords

Drosophila; climbing assay; negative geotaxis; DART; DNA damage response; p53

Funding

  1. UK Biotechnology and Biological Sciences Research Council [BB/N008472/1]
  2. BBSRC [BB/N008472/1] Funding Source: UKRI

Ask authors/readers for more resources

The fruit fly, Drosophila, is commonly used to study late-onset neurodegenerative diseases due to the combination of powerful genetic tools, cheap and simple husbandry and short lifespan. One widely-used measure of disease progression is the age-dependent decline in motor performance that manifests in most Drosophila neurodegeneration models. This is usually quantified using a simple climbing assay. However, the standard climbing assay lacks sensitivity and suffers from high variability meaning large numbers of flies are needed or bespoke apparatus and software solutions. Here, we present a modification of the open-source, MATLAB-based, DART software to measure the decline in startle response with age. We demonstrate that the DART setup is more sensitive to the motor performance decline induced by adult-onset neuronal expression of amyloid beta (A beta) peptides than a traditional climbing assay despite using smaller cohorts of flies. DART also has the potential to generate multiple metrics of motor behaviour during the startle response. The software requires no coding skills to operate and the required apparatus can be purchased commercially. Therefore, DART is a more useful method than the climbing assay for longitudinal assays of motor performance and will enable higher-throughput screen for genetic and pharmacological modifiers of neurodegeneration. In our proof-of-concept screen for modifiers of A beta-dependent phenotypes, we identified that in vivo knock-down of p53 in adult neurons is neuroprotective. This supports recent work targeting p53 in vitro and demonstrates the potential for DART to be used to screen for targets that ameliorate neurodegeneration.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.0
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

Review Biochemistry & Molecular Biology

The neuronal ceroid lipofuscinoses: Opportunities from model systems

Kiterie M. E. Faller, Rodrigo Gutierrez-Quintana, Alamin Mohammed, Ahad A. Rahim, Richard I. Tuxworth, Kim Wager, Michael Bond

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2015)

Review Biochemistry & Molecular Biology

Dysregulation of autophagy as a common mechanism in lysosomal storage diseases

Elena Seranova, Kyle J. Connolly, Malgorzata Zatyka, Tatiana R. Rosenstock, Timothy Barrett, Richard I. Tuxworth, Sovan Sarkar

SIGNALLING MECHANISMS IN AUTOPHAGY (2017)

Article Neurosciences

in vivo localization of the neuronal ceroid lipofuscinosis proteins, CLN3 and CLN7, at endogenous expression levels

Alamin Mohammed, Megan B. O'Hare, Alice Warley, Guy Tear, Richard I. Tuxworth

NEUROBIOLOGY OF DISEASE (2017)

Article Biochemistry & Molecular Biology

The Batten disease gene CLN3 is required for the response to oxidative stress

Richard I. Tuxworth, Haiyang Chen, Valerie Vivancos, Nancy Carvajal, Xun Huang, Guy Tear

HUMAN MOLECULAR GENETICS (2011)

Article Biology

Modification of the Drosophila model of in vivo Tau toxicity reveals protective phosphorylation by GSK3β

Giulia Povellato, Richard I. Tuxworth, Diane P. Hanger, Guy Tear

BIOLOGY OPEN (2014)

Article Biochemistry & Molecular Biology

The contribution of multicellular model organisms to neuronal ceroid lipofuscinosis research

Robert J. Huber, Stephanie M. Hughes, Wenfei Liu, Alan Morgan, Richard Tuxworth, Claire Russell

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2020)

Article Multidisciplinary Sciences

The neuronal ceroid lipofuscinosis protein Cln7 functions in the postsynaptic cell to regulate synapse development

Kyle J. Connolly, Megan B. O'Hare, Alamin Mohammed, Katelyn M. Aitchison, Niki C. Anthoney, Matthew J. Taylor, Bryan A. Stewart, Richard I. Tuxworth, Guy Tear

SCIENTIFIC REPORTS (2019)

Article Multidisciplinary Sciences

Inhibition of Chk2 promotes neuroprotection, axon regeneration, and functional recovery after CNS injury

Matthew J. Taylor, Adam M. Thompson, Sharif Alhajlah, Richard Tuxworth, Zubair Ahmed

Summary: DNA double-strand breaks play a crucial role in neurological conditions, and targeting the ATM-Chk2 pathway can slow down neural decline and promote neuroprotection by inhibiting nonhomologous end-joining.

SCIENCE ADVANCES (2022)

Article Clinical Neurology

Attenuating the DNA damage response to double-strand breaks restores function in models of CNS neurodegeneration

Richard Tuxworth, Matthew J. Taylor, Ane Martin Anduaga, Alaa Hussien-Ali, Sotiroula Chatzimatthaiou, Joanne Longland, Adam M. Thompson, Sharif Almutiri, Pavlos Alifragis, Charalambos P. Kyriacou, Boris Kysela, Zubair Ahmed

BRAIN COMMUNICATIONS (2019)

No Data Available