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Histone H3 and H4 Modifications Point to Transcriptional Suppression as a Component of Winter Freeze Tolerance in the Gall Fly Eurosta solidaginis
by
Storey, Kenneth B.
, Bloskie, Tighe
in
Animals
/ Cell division
/ Cold
/ Cold Temperature
/ Cryoprotective Agents - metabolism
/ Cryoprotective Agents - pharmacology
/ DNA methylation
/ Enzymes
/ Epigenetics
/ Freezing
/ Genes
/ Genetic engineering
/ Histones - genetics
/ Histones - metabolism
/ Insects
/ Larva - metabolism
/ Metabolism
/ Proteins
/ Reptiles & amphibians
/ Tephritidae - metabolism
/ Yeast
2023
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Histone H3 and H4 Modifications Point to Transcriptional Suppression as a Component of Winter Freeze Tolerance in the Gall Fly Eurosta solidaginis
by
Storey, Kenneth B.
, Bloskie, Tighe
in
Animals
/ Cell division
/ Cold
/ Cold Temperature
/ Cryoprotective Agents - metabolism
/ Cryoprotective Agents - pharmacology
/ DNA methylation
/ Enzymes
/ Epigenetics
/ Freezing
/ Genes
/ Genetic engineering
/ Histones - genetics
/ Histones - metabolism
/ Insects
/ Larva - metabolism
/ Metabolism
/ Proteins
/ Reptiles & amphibians
/ Tephritidae - metabolism
/ Yeast
2023
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Histone H3 and H4 Modifications Point to Transcriptional Suppression as a Component of Winter Freeze Tolerance in the Gall Fly Eurosta solidaginis
by
Storey, Kenneth B.
, Bloskie, Tighe
in
Animals
/ Cell division
/ Cold
/ Cold Temperature
/ Cryoprotective Agents - metabolism
/ Cryoprotective Agents - pharmacology
/ DNA methylation
/ Enzymes
/ Epigenetics
/ Freezing
/ Genes
/ Genetic engineering
/ Histones - genetics
/ Histones - metabolism
/ Insects
/ Larva - metabolism
/ Metabolism
/ Proteins
/ Reptiles & amphibians
/ Tephritidae - metabolism
/ Yeast
2023
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Histone H3 and H4 Modifications Point to Transcriptional Suppression as a Component of Winter Freeze Tolerance in the Gall Fly Eurosta solidaginis
Journal Article
Histone H3 and H4 Modifications Point to Transcriptional Suppression as a Component of Winter Freeze Tolerance in the Gall Fly Eurosta solidaginis
2023
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Overview
The goldenrod gall fly (Eurosta solidaginis) is a well-studied model of insect freeze tolerance. In situations of prolonged winter subzero temperatures, larvae of E. solidaginis accept ice penetration throughout extracellular spaces while protecting the intracellular environment by producing extreme amounts of glycerol and sorbitol as cryoprotectants. Hypometabolism (diapause) is implemented, and energy use is reprioritized to essential pathways. Gene transcription is one energy-expensive process likely suppressed over the winter, in part, due to epigenetic controls. The present study profiled the prevalence of 24 histone H3/H4 modifications of E. solidaginis larvae after 3-week acclimations to decreasing environmental temperatures (5 °C, −5 °C and −15 °C). Using immunoblotting, the data show freeze-mediated reductions (p < 0.05) in seven permissive histone modifications (H3K27me1, H4K20me1, H3K9ac, H3K14ac, H3K27ac, H4K8ac, H3R26me2a). Along with the maintenance of various repressive marks, the data are indicative of a suppressed transcriptional state at subzero temperatures. Elevated nuclear levels of histone H4, but not histone H3, were also observed in response to both cold and freeze acclimation. Together, the present study provides evidence for epigenetic-mediated transcriptional suppression in support of the winter diapause state and freeze tolerance of E. solidaginis.
Publisher
MDPI AG,MDPI
Subject
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