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Redundant functions of the SLC5A transporters Rumpel Kumpel and Bumpel in ensheathing glial cells
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Abstract
Neuronal processing is energy demanding, and relies on sugar metabolism as an energy source. To provide a constant metabolite supply neurons and glial cells express many glucose and lactate transporters of the solute carrier (SLC) 5A family. Here we dissect the partially redundant functions of three highly related glia specific Drosophila genes encoding SLC5A proteins, Rumpel, Bumpel and Kumpel. While knockdown of
rumpel
causes several behavioral phenotypes, they are less prominent in
rumpel
mutants.
bumpel
and
kumpel
mutants are viable and fertile, lacking discernible phenotypes. However, in
bumpel kumpel
double mutants and to an even greater extent in
rumpel bumpel kumpel
triple mutants oogenesis is disrupted at the onset of the vitollegenic phase. This indicates at least partially redundant functions between these genes. Rescue experiments exploring this effect indicate that oogenesis can be affected by CNS glial cells. Moreover, expression of heterologous mammalian SLC5A transporter proteins, with known transport properties, suggest that Bumpel and/or Kumpel transport glucose or lactate. Overall, our results imply a redundancy in SLC5A nutrient sensing functions in Drosophila glial cells, affecting ovarian development and behavior.
Title: Redundant functions of the SLC5A transporters Rumpel Kumpel and Bumpel in ensheathing glial cells
Description:
Abstract
Neuronal processing is energy demanding, and relies on sugar metabolism as an energy source.
To provide a constant metabolite supply neurons and glial cells express many glucose and lactate transporters of the solute carrier (SLC) 5A family.
Here we dissect the partially redundant functions of three highly related glia specific Drosophila genes encoding SLC5A proteins, Rumpel, Bumpel and Kumpel.
While knockdown of
rumpel
causes several behavioral phenotypes, they are less prominent in
rumpel
mutants.
bumpel
and
kumpel
mutants are viable and fertile, lacking discernible phenotypes.
However, in
bumpel kumpel
double mutants and to an even greater extent in
rumpel bumpel kumpel
triple mutants oogenesis is disrupted at the onset of the vitollegenic phase.
This indicates at least partially redundant functions between these genes.
Rescue experiments exploring this effect indicate that oogenesis can be affected by CNS glial cells.
Moreover, expression of heterologous mammalian SLC5A transporter proteins, with known transport properties, suggest that Bumpel and/or Kumpel transport glucose or lactate.
Overall, our results imply a redundancy in SLC5A nutrient sensing functions in Drosophila glial cells, affecting ovarian development and behavior.
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