author_facet Zhao, Yanmei
Sun, Hui
Lu, Jun
Li, Xiaoxue
Chen, Xia
Tao, Dan
Huang, Weifeng
Huang, Baiqu
Zhao, Yanmei
Sun, Hui
Lu, Jun
Li, Xiaoxue
Chen, Xia
Tao, Dan
Huang, Weifeng
Huang, Baiqu
author Zhao, Yanmei
Sun, Hui
Lu, Jun
Li, Xiaoxue
Chen, Xia
Tao, Dan
Huang, Weifeng
Huang, Baiqu
spellingShingle Zhao, Yanmei
Sun, Hui
Lu, Jun
Li, Xiaoxue
Chen, Xia
Tao, Dan
Huang, Weifeng
Huang, Baiqu
Journal of Experimental Biology
Lifespan extension and elevatedhspgene expression inDrosophilacaused by histone deacetylase inhibitors
Insect Science
Molecular Biology
Animal Science and Zoology
Aquatic Science
Physiology
Ecology, Evolution, Behavior and Systematics
author_sort zhao, yanmei
spelling Zhao, Yanmei Sun, Hui Lu, Jun Li, Xiaoxue Chen, Xia Tao, Dan Huang, Weifeng Huang, Baiqu 1477-9145 0022-0949 The Company of Biologists Insect Science Molecular Biology Animal Science and Zoology Aquatic Science Physiology Ecology, Evolution, Behavior and Systematics http://dx.doi.org/10.1242/jeb.01439 <jats:title>SUMMARY</jats:title><jats:p>The heat shock proteins (Hsps) play a positive role in lifespan determination, and histone acetylation has been shown to be involved in transcription of hsp genes in Drosophila. To further determine if hsp22 and hsp70 expression is correlated with lifespan, and if histone acetylation participates in this process, RNA levels for hsp22 and hsp70 were analyzed throughout the lifespan in the long-lived and short-lived iso-female lines. The results showed that hsp22 and hsp70 RNA levels were higher in long-lived line than in short-lived line and that the long-lived flies responded more rapidly to heat but were more tolerant to high temperature. Moreover, we investigated the influences of histone acetylation modification on longevity and on hsp gene expression by using histone deacetylase (HDAC) inhibitors TSA and BuA. The results demonstrated that both inhibitors were able to extend the lifespan and promote hsp22 and hsp70 expression. However, the optimal concentrations of these inhibitors, and probably the mechanisms of their actions, vary with the genetic background. In addition, we showed that HDAC inhibitors caused the hyperacetylation of core histone H3,implicating the involvement of chromatin modulation in hsp gene transcription. These data suggested a close correlation among histone acetylation, hsp gene expression and longevity in D. melanogaster.</jats:p> Lifespan extension and elevated<i>hsp</i>gene expression in<i>Drosophila</i>caused by histone deacetylase inhibitors Journal of Experimental Biology
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recordtype ai
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series Journal of Experimental Biology
source_id 49
title Lifespan extension and elevatedhspgene expression inDrosophilacaused by histone deacetylase inhibitors
title_unstemmed Lifespan extension and elevatedhspgene expression inDrosophilacaused by histone deacetylase inhibitors
title_full Lifespan extension and elevatedhspgene expression inDrosophilacaused by histone deacetylase inhibitors
title_fullStr Lifespan extension and elevatedhspgene expression inDrosophilacaused by histone deacetylase inhibitors
title_full_unstemmed Lifespan extension and elevatedhspgene expression inDrosophilacaused by histone deacetylase inhibitors
title_short Lifespan extension and elevatedhspgene expression inDrosophilacaused by histone deacetylase inhibitors
title_sort lifespan extension and elevated<i>hsp</i>gene expression in<i>drosophila</i>caused by histone deacetylase inhibitors
topic Insect Science
Molecular Biology
Animal Science and Zoology
Aquatic Science
Physiology
Ecology, Evolution, Behavior and Systematics
url http://dx.doi.org/10.1242/jeb.01439
publishDate 2005
physical 697-705
description <jats:title>SUMMARY</jats:title><jats:p>The heat shock proteins (Hsps) play a positive role in lifespan determination, and histone acetylation has been shown to be involved in transcription of hsp genes in Drosophila. To further determine if hsp22 and hsp70 expression is correlated with lifespan, and if histone acetylation participates in this process, RNA levels for hsp22 and hsp70 were analyzed throughout the lifespan in the long-lived and short-lived iso-female lines. The results showed that hsp22 and hsp70 RNA levels were higher in long-lived line than in short-lived line and that the long-lived flies responded more rapidly to heat but were more tolerant to high temperature. Moreover, we investigated the influences of histone acetylation modification on longevity and on hsp gene expression by using histone deacetylase (HDAC) inhibitors TSA and BuA. The results demonstrated that both inhibitors were able to extend the lifespan and promote hsp22 and hsp70 expression. However, the optimal concentrations of these inhibitors, and probably the mechanisms of their actions, vary with the genetic background. In addition, we showed that HDAC inhibitors caused the hyperacetylation of core histone H3,implicating the involvement of chromatin modulation in hsp gene transcription. These data suggested a close correlation among histone acetylation, hsp gene expression and longevity in D. melanogaster.</jats:p>
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author Zhao, Yanmei, Sun, Hui, Lu, Jun, Li, Xiaoxue, Chen, Xia, Tao, Dan, Huang, Weifeng, Huang, Baiqu
author_facet Zhao, Yanmei, Sun, Hui, Lu, Jun, Li, Xiaoxue, Chen, Xia, Tao, Dan, Huang, Weifeng, Huang, Baiqu, Zhao, Yanmei, Sun, Hui, Lu, Jun, Li, Xiaoxue, Chen, Xia, Tao, Dan, Huang, Weifeng, Huang, Baiqu
author_sort zhao, yanmei
container_issue 4
container_start_page 697
container_title Journal of Experimental Biology
container_volume 208
description <jats:title>SUMMARY</jats:title><jats:p>The heat shock proteins (Hsps) play a positive role in lifespan determination, and histone acetylation has been shown to be involved in transcription of hsp genes in Drosophila. To further determine if hsp22 and hsp70 expression is correlated with lifespan, and if histone acetylation participates in this process, RNA levels for hsp22 and hsp70 were analyzed throughout the lifespan in the long-lived and short-lived iso-female lines. The results showed that hsp22 and hsp70 RNA levels were higher in long-lived line than in short-lived line and that the long-lived flies responded more rapidly to heat but were more tolerant to high temperature. Moreover, we investigated the influences of histone acetylation modification on longevity and on hsp gene expression by using histone deacetylase (HDAC) inhibitors TSA and BuA. The results demonstrated that both inhibitors were able to extend the lifespan and promote hsp22 and hsp70 expression. However, the optimal concentrations of these inhibitors, and probably the mechanisms of their actions, vary with the genetic background. In addition, we showed that HDAC inhibitors caused the hyperacetylation of core histone H3,implicating the involvement of chromatin modulation in hsp gene transcription. These data suggested a close correlation among histone acetylation, hsp gene expression and longevity in D. melanogaster.</jats:p>
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spelling Zhao, Yanmei Sun, Hui Lu, Jun Li, Xiaoxue Chen, Xia Tao, Dan Huang, Weifeng Huang, Baiqu 1477-9145 0022-0949 The Company of Biologists Insect Science Molecular Biology Animal Science and Zoology Aquatic Science Physiology Ecology, Evolution, Behavior and Systematics http://dx.doi.org/10.1242/jeb.01439 <jats:title>SUMMARY</jats:title><jats:p>The heat shock proteins (Hsps) play a positive role in lifespan determination, and histone acetylation has been shown to be involved in transcription of hsp genes in Drosophila. To further determine if hsp22 and hsp70 expression is correlated with lifespan, and if histone acetylation participates in this process, RNA levels for hsp22 and hsp70 were analyzed throughout the lifespan in the long-lived and short-lived iso-female lines. The results showed that hsp22 and hsp70 RNA levels were higher in long-lived line than in short-lived line and that the long-lived flies responded more rapidly to heat but were more tolerant to high temperature. Moreover, we investigated the influences of histone acetylation modification on longevity and on hsp gene expression by using histone deacetylase (HDAC) inhibitors TSA and BuA. The results demonstrated that both inhibitors were able to extend the lifespan and promote hsp22 and hsp70 expression. However, the optimal concentrations of these inhibitors, and probably the mechanisms of their actions, vary with the genetic background. In addition, we showed that HDAC inhibitors caused the hyperacetylation of core histone H3,implicating the involvement of chromatin modulation in hsp gene transcription. These data suggested a close correlation among histone acetylation, hsp gene expression and longevity in D. melanogaster.</jats:p> Lifespan extension and elevated<i>hsp</i>gene expression in<i>Drosophila</i>caused by histone deacetylase inhibitors Journal of Experimental Biology
spellingShingle Zhao, Yanmei, Sun, Hui, Lu, Jun, Li, Xiaoxue, Chen, Xia, Tao, Dan, Huang, Weifeng, Huang, Baiqu, Journal of Experimental Biology, Lifespan extension and elevatedhspgene expression inDrosophilacaused by histone deacetylase inhibitors, Insect Science, Molecular Biology, Animal Science and Zoology, Aquatic Science, Physiology, Ecology, Evolution, Behavior and Systematics
title Lifespan extension and elevatedhspgene expression inDrosophilacaused by histone deacetylase inhibitors
title_full Lifespan extension and elevatedhspgene expression inDrosophilacaused by histone deacetylase inhibitors
title_fullStr Lifespan extension and elevatedhspgene expression inDrosophilacaused by histone deacetylase inhibitors
title_full_unstemmed Lifespan extension and elevatedhspgene expression inDrosophilacaused by histone deacetylase inhibitors
title_short Lifespan extension and elevatedhspgene expression inDrosophilacaused by histone deacetylase inhibitors
title_sort lifespan extension and elevated<i>hsp</i>gene expression in<i>drosophila</i>caused by histone deacetylase inhibitors
title_unstemmed Lifespan extension and elevatedhspgene expression inDrosophilacaused by histone deacetylase inhibitors
topic Insect Science, Molecular Biology, Animal Science and Zoology, Aquatic Science, Physiology, Ecology, Evolution, Behavior and Systematics
url http://dx.doi.org/10.1242/jeb.01439