bioRxiv Science⌕ Search

Biology subjects

Bretscher, H.

Publications and source records attributed to Bretscher, H..

2 recordsLinked to original sources

TGFbeta/Activin Signaling links glycogen homeostasis to mtDNA expression in Drosophila

Maintaining metabolic homeostasis requires coordinated nutrient utilization between intracellular organelles and across multiple organ systems. Many organs rely heavily on mitochondria to generate (ATP) from glucose, or stored glycogen. Proteins required for ATP generation are encoded in both nuclear and mitochondrial DNA (mtDNA). We show that motoneuron to muscle signaling by the TGF{beta}/Activin family member Act{beta} positively regulates glycogen levels during Drosophila development. Remarkably, we find that levels of stored glycogen are unaffected by altering cytoplasmic glucose catabolism. Instead, Act{beta} loss reduces levels of mtDNA and nuclearly encoded genes required for mtDNA replication, transcription and translation. Direct RNAi mediated knockdown of these same nuclearly encoded mtDNA expression factors also results in decreased glycogen stores. Lastly, we find that expressing an activated form of the type I receptor Baboon in muscle restores both glycogen and mtDNA levels in act{beta} mutants, thereby confirming a direct link between Act{beta} signaling, glycogen homeostasis and mtDNA expression. Key PointsO_LIThe Drosophila TGF{beta} family member Act{beta} signals from motor neuron to muscle positively regulating glycogen levels C_LIO_LIAct{beta} positively regulates nuclearly encoded factors required for mtDNA expression C_LIO_LIGenes involved in mtDNA expression directly regulate glycogen stores C_LIO_LIExpressing an activated receptor in muscle restores glycogen and mtDNA in act{beta} mutants C_LI O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=175 SRC="FIGDIR/small/600699v2_ufig1.gif" ALT="Figure 1"> View larger version (32K): org.highwire.dtl.DTLVardef@1bafafaorg.highwire.dtl.DTLVardef@b34255org.highwire.dtl.DTLVardef@c80b05org.highwire.dtl.DTLVardef@14b9b9e_HPS_FORMAT_FIGEXP M_FIG C_FIG

cell biology↗

Knockdown of Atg1 or Atg18 in adult adipocytes impairs lipophagy and reduces lifespan of fruit flies (Drosophila melanogaster)

Autophagy, a lysosome-based eukaryotic cellular degradation system, has previously been implicated in lifespan regulation in different animal models. In this report, we show that expression of the RNAi transgenes targeting the transcripts of the key autophagy genes such as Atg1 or Atg18 in adult fly muscle or glia does not affect the overall levels of autophagosomes in those tissues and does not change the lifespan of the tested flies, but lifespan reduction phenotype has become apparent when Atg1 RNAi or Atg18 RNAi is expressed in a non-tissue-specific manner through a Tub-Gal4 in adult flies or after lipophagy is eradicated through the knockdown of Atg1 or Atg18 in adult fly adipocytes. Lifespan reduction was also observed when Atg1 or Atg18 was knocked down in adult fly enteroblasts and middle gut stem cells. Over-expression of wildtype Atg1 in adult fly muscle or adipocytes reduces lifespan. High levels of ubiquitinated protein aggregates could be the culprit of the reduced lifespan of Atg1 over-expression flies. Our research data presented here have highlighted the important functions of the key autophagy genes in adult fly adipocytes, enteroblasts, and midgut stem cells for lifespan regulation and their undetermined functions in adult fly muscle and glia. SummaryIn this research, we have demonstrated that the key autophagy genes play important roles in fly lifespan regulation through adult adipose tissues, enteroblasts, and middle gut stem cells.

genetics↗