Abstract:The Nimrod gene cluster, located on the second chromosome of Drosophila melanogaster, is the largest synthenic unit of the Drosophila genome. Nimrod genes show blood cell specific expression and code for phagocytosis receptors that play a major role in fruit fly innate immune functions. We previously identified three homologous genes (vajk-1, vajk-2 and vajk-3) located within the Nimrod cluster, which are unrelated to the Nimrod genes, but are homologous to a fourth gene (vajk-4) located outside the cluster. H… Show more
“…The vajk-1 gene is located within the Nimrod gene cluster on chromosome 2, the largest syntenic unit in the genome ( Somogyi et al 2010 ; Cinege et al 2017 ). Genes of the Nimrod cluster have been suggested to contribute to innate immune response ( Kurucz et al 2007 ).…”
Section: Resultsmentioning
confidence: 99%
“…However, vajk genes are not related to the Nimrod genes, which are involved in the innate immune defense. The vajk gene members are conserved in insects, but their function is unknown ( Somogyi et al 2010 ; Cinege et al 2017 ). Our results suggest that vajk-1 could be involved in the memory formation process.…”
Memory formation is achieved by genetically tightly controlled molecular pathways that result in a change of synaptic strength and synapse organization. While for short-term memory traces, rapidly acting biochemical pathways are in place, the formation of long-lasting memories requires changes in the transcriptional program of a cell. Although many genes involved in learning and memory formation have been identified, little is known about the genetic mechanisms required for changing the transcriptional program during different phases of long-term memory (LTM) formation. With Drosophila melanogaster as a model system, we profiled transcriptomic changes in the mushroom body—a memory center in the fly brain—at distinct time intervals during appetitive olfactory LTM formation using the targeted DamID technique. We describe the gene expression profiles during these phases and tested 33 selected candidate genes for deficits in LTM formation using RNAi knockdown. We identified 10 genes that enhance or decrease memory when knocked-down in the mushroom body. For vajk-1 and hacd1—the two strongest hits—we gained further support for their crucial role in appetitive learning and forgetting. These findings show that profiling gene expression changes in specific cell-types harboring memory traces provides a powerful entry point to identify new genes involved in learning and memory. The presented transcriptomic data may further be used as resource to study genes acting at different memory phases.
“…The vajk-1 gene is located within the Nimrod gene cluster on chromosome 2, the largest syntenic unit in the genome ( Somogyi et al 2010 ; Cinege et al 2017 ). Genes of the Nimrod cluster have been suggested to contribute to innate immune response ( Kurucz et al 2007 ).…”
Section: Resultsmentioning
confidence: 99%
“…However, vajk genes are not related to the Nimrod genes, which are involved in the innate immune defense. The vajk gene members are conserved in insects, but their function is unknown ( Somogyi et al 2010 ; Cinege et al 2017 ). Our results suggest that vajk-1 could be involved in the memory formation process.…”
Memory formation is achieved by genetically tightly controlled molecular pathways that result in a change of synaptic strength and synapse organization. While for short-term memory traces, rapidly acting biochemical pathways are in place, the formation of long-lasting memories requires changes in the transcriptional program of a cell. Although many genes involved in learning and memory formation have been identified, little is known about the genetic mechanisms required for changing the transcriptional program during different phases of long-term memory (LTM) formation. With Drosophila melanogaster as a model system, we profiled transcriptomic changes in the mushroom body—a memory center in the fly brain—at distinct time intervals during appetitive olfactory LTM formation using the targeted DamID technique. We describe the gene expression profiles during these phases and tested 33 selected candidate genes for deficits in LTM formation using RNAi knockdown. We identified 10 genes that enhance or decrease memory when knocked-down in the mushroom body. For vajk-1 and hacd1—the two strongest hits—we gained further support for their crucial role in appetitive learning and forgetting. These findings show that profiling gene expression changes in specific cell-types harboring memory traces provides a powerful entry point to identify new genes involved in learning and memory. The presented transcriptomic data may further be used as resource to study genes acting at different memory phases.
“…NimC1 was initially identified as an antigen for the plasmatocyte specific monoclonal antibody P1. It belongs to the Nimrod gene family that has been implicated in the cellular innate immune response in Drosophila [46], [47]. A previous study pointed to the importance of NimC1 in the phagocytosis of bacteria, since RNAi-mediated silencing of this gene resulted in decreased S.…”
Eater and NimC1 are transmembrane receptors of the Drosophila Nimrod family, specifically expressed in hemocytes, the insect blood cells. Previous ex vivo and in vivo RNAi studies have pointed to their role in the phagocytosis of bacteria. Here, we have created a novel null mutant in NimC1 to re-evaluate the role of NimC1, alone or in combination with Eater, in the cellular immune response. We show that NimC1 functions as an adhesion molecule ex vivo, but in contrast to Eater is not required for hemocyte sessility in vivo. Ex vivo phagocytosis assays and electron microscopy experiments confirmed that Eater is the main phagocytic receptor for
“…The vajk-1 gene is located within the Nimrod gene cluster on chromosome 2, the largest syntenic unit in the genome (Somogyi et al 2010; Cinege et al 2017). Genes of the Nimrod cluster have been suggested to be contributing to innate immune response (Kurucz et al 2007).…”
Memory formation is achieved by genetically tightly controlled molecular pathways genes for deficits in long-term memory formation using RNAi knockdown. We identified 10 genes that enhance or decrease memory when knocked-down in the 2 6 mushroom body. For vajk-1 and hacd1, the two strongest hits, we gained further study genes acting at different memory phases.
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