Affiliation:
1. Genes Circuits Rhythms and Neuropathology, Brain Plasticity Unit, CNRS, ESPCI Paris, PSL Research University
2. Laboratory of Metabolic Diseases
3. Integrated Physiology of the Brain Arousal Systems (WAKING), Lyon Neuroscience Research Centre
4. Dipartimento di Scienze Agroalimentari
5. Metabolomic and Proteomic Biochemistry Laboratory, Necker-Enfants Malades Hospital
Abstract
Adenine phosphoribosyltransferase (APRT) and hypoxanthine-guanine phosphoribosyltransferase (HGPRT) are two structurally related enzymes involved in purine recycling in humans. Inherited mutations that suppress HGPRT activity are associated with Lesch-Nyhan disease (LND), a rare X-linked metabolic and neurological disorder in children, characterized by hyperuricemia, dystonia and compulsive self-injury. To date, no treatment is available for these neurological defects and no animal model recapitulates all symptoms of LND patients. Here we studied LND-related mechanisms in the fruit fly. By combining enzymatic assays and phylogenetic analysis, we confirm that no HGPRT activity is expressed in
Drosophila melanogaster
, making the APRT homologue (Aprt) the only purine-recycling enzyme in this organism. Whereas APRT deficiency does not trigger neurological defects in humans, we observed that
Drosophila Aprt
mutants show both metabolic and neurobehavioral disturbances, including increased uric acid levels, locomotor impairments, sleep alterations, seizure-like behavior, reduced lifespan, and reduction of adenosine signaling and content. Locomotor defects could be rescued by Aprt re-expression in neurons and reproduced by knocking down
Aprt
selectively in the protocerebral anterior medial (PAM) dopaminergic neurons, the mushroom bodies or glia subsets. Ingestion of allopurinol rescued uric acid levels in
Aprt
-deficient mutants but not neurological defects, as is the case in LND patients, while feeding adenosine or
N
6
-methyladenosine (m
6
A) during development fully rescued the epileptic behavior. Intriguingly, pan-neuronal expression of an LND-associated mutant form of human HGPRT (I42T), but not the wild-type enzyme, resulted in early locomotor defects and seizure in flies, similar to
Aprt
deficiency. Overall, our results suggest that
Drosophila
could be used in different ways to better understand LND and seek a cure for this dramatic disease.
Publisher
eLife Sciences Publications, Ltd