@article {648,
	title = {Gene expression of heat-shock proteins (Hsp23, Hsp70 and Hsp90) during and after larval diapause in the blow fly Lucilia sericata},
	volume = {51},
	year = {Submitted},
	note = {08-10-200906-02-2012NormalDepartment of Bio- and Geosciences, Graduate School of Science, Osaka City University, Sumiyoshi, Osaka 558-8585, Japan.enghttp://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve\&db=pubmed\&dopt=Abstract\&list_uids=15993128},
	pages = {641 - 647},
	abstract = {Genes encoding heat-shock protein 23 (Hsp23), Hsp70 and Hsp90 were cloned from Lucilia sericata to examine whether their expression is related to the regulation of its larval diapause. The level of all three Hsps mRNAs was consistently low irrespective of diapause status. These results indicate that expression of Hsp23, Hsp70 and Hsp90 is not regulated in response to diapause, in contrast to the flesh fly Sarcophaga crassipalpis that shows upregulation of Hsp23 and Hsp70 and downregulation of Hsp90 during its pupal diapause. On the other hand, Hsp90 transcripts were regulated developmentally in nondiapause larvae of L. sericata, i.e., they were at low levels after cessation of feeding but were considerably upregulated a day before pupariation, suggesting that Hsp90 is involved in a developmental process that occurs between the cessation of feeding and pupariation. When diapause larvae were transferred to all of the conditions that terminate diapause and allow postdiapause development, Hsp90 transcripts were promptly upregulated. These results indicate that Hsp90 may serve as an early marker to predict diapause termination in this species.},
	keywords = {Animals, Diptera/*metabolism, Gene Expression Regulation, Developmental/*physiology, Heat-Shock Proteins/*biosynthesis, Hot Temperature, Insect Proteins/*biosynthesis, Larva/metabolism, Photoperiod, Tissue Distribution, Transcription, Genetic/physiology},
	author = {Tachibana, S. and Numata, H. and Goto, S. G.}
}
@article {543,
	title = {Fat-body remodeling in Drosophila melanogaster},
	volume = {44},
	year = {Submitted},
	note = {08-10-200906-02-2012Normalenghttp://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve\&db=pubmed\&dopt=Abstract\&list_uids=16868920},
	pages = {396 - 400},
	abstract = {The remodeling of the larval fat body is observed in many insects during metamorphosis, but little is known about the physiological importance or the regulation of this process. In Drosophila melanogaster, fat-body remodeling involves the dissociation of the fat body into individual fat cells, which persist throughout pupal development but are later removed by cell death in the young adult. Inhibition of fat-body dissociation is associated with pharate adult lethality and thus is likely to be an essential developmental event. As a start toward understanding the role of fat-body remodeling in the life history of insects, we carried out a detailed study of fat-body disassociation in D. melanogaster using fluorescent microscopy, and tested whether this process is mediated by hemocytes as proposed for fat-body remodeling in Sarcophaga peregrina. We identified and correlated stereotypic events in fat-body dissociation with developmental changes during metamorphosis, and have demonstrated by cell ablation studies that fat-body remodeling in D. melanogaster is a hemocyte independent process.},
	keywords = {Animals, Cell Shape, development/*metabolism, Drosophila melanogaster/genetics/growth \&amp, Fat Body/cytology/*metabolism, Genes, Insect, Green Fluorescent Proteins/metabolism, Hemocytes/cytology/physiology, Larva/metabolism, Metamorphosis, Biological, Microscopy, Fluorescence, Mutation, Pupa/genetics/metabolism},
	author = {Nelliot, A. and Bond, N. and Hoshizaki, D. K.}
}
