Identifying sexual differentiation genes that affect Drosophila life span
<p>Abstract</p> <p>Background</p> <p>Sexual differentiation often has significant effects on life span and aging phenotypes. For example, males and females of several species have different life spans, and genetic and environmental manipulations that affect life span of...
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| Format: | Article |
| Language: | English |
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BMC
2009-12-01
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| Series: | BMC Geriatrics |
| Online Access: | http://www.biomedcentral.com/1471-2318/9/56 |
| _version_ | 1818806755620028416 |
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| author | Tower John Landis Gary N Ford Daniel Shen Jie |
| author_facet | Tower John Landis Gary N Ford Daniel Shen Jie |
| author_sort | Tower John |
| collection | DOAJ |
| description | <p>Abstract</p> <p>Background</p> <p>Sexual differentiation often has significant effects on life span and aging phenotypes. For example, males and females of several species have different life spans, and genetic and environmental manipulations that affect life span often have different magnitude of effect in males versus females. Moreover, the presence of a differentiated germ-line has been shown to affect life span in several species, including <it>Drosophila </it>and <it>C. elegans</it>.</p> <p>Methods</p> <p>Experiments were conducted to determine how alterations in sexual differentiation gene activity might affect the life span of <it>Drosophila melanogaster. Drosophila </it>females heterozygous for the <it>tudor[1]</it> mutation produce normal offspring, while their homozygous sisters produce offspring that lack a germ line. To identify additional sexual differentiation genes that might affect life span, the conditional transgenic system Geneswitch was employed, whereby feeding adult flies or developing larvae the drug RU486 causes the over-expression of selected UAS-transgenes.</p> <p>Results</p> <p>In this study germ-line ablation caused by the maternal <it>tudor[1]</it> mutation was examined in a long-lived genetic background, and was found to increase life span in males but not in females, consistent with previous reports. Fitting the data to a Gompertz-Makeham model indicated that the maternal <it>tudor[1]</it> mutation increases the life span of male progeny by decreasing age-independent mortality. The Geneswitch system was used to screen through several UAS-type and EP-type P element mutations in genes that regulate sexual differentiation, to determine if additional sex-specific effects on life span would be obtained. Conditional over-expression of <it>transformer </it>female isoform (<it>traF) </it>during development produced male adults with inhibited sexual differentiation, however this caused no significant change in life span. Over-expression of <it>doublesex </it>female isoform (<it>dsxF) </it>during development was lethal to males, and produced a limited number of female escapers, whereas over-expression of <it>dsxF </it>specifically in adults greatly reduced both male and female life span. Similarly, over-expression of <it>fruitless </it>male isoform <it>A </it>(<it>fru-MA</it>) during development was lethal to both males and females, whereas over-expression of <it>fru-MA </it>in adults greatly reduced both male and female life span.</p> <p>Conclusion</p> <p>Manipulation of sexual differentiation gene expression specifically in the adult, after morphological sexual differentiation is complete, was still able to affect life span. In addition, by manipulating gene expression during development, it was possible to significantly alter morphological sexual differentiation without a significant effect on adult life span. The data demonstrate that manipulation of sexual differentiation pathway genes either during development or in adults can affect adult life span.</p> |
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| id | doaj.art-bf0e474bf51d498a9aeff8fc1fec54e5 |
| institution | Directory Open Access Journal |
| issn | 1471-2318 |
| language | English |
| last_indexed | 2024-12-18T19:14:49Z |
| publishDate | 2009-12-01 |
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| series | BMC Geriatrics |
| spelling | doaj.art-bf0e474bf51d498a9aeff8fc1fec54e52022-12-21T20:56:10ZengBMCBMC Geriatrics1471-23182009-12-01915610.1186/1471-2318-9-56Identifying sexual differentiation genes that affect Drosophila life spanTower JohnLandis Gary NFord DanielShen Jie<p>Abstract</p> <p>Background</p> <p>Sexual differentiation often has significant effects on life span and aging phenotypes. For example, males and females of several species have different life spans, and genetic and environmental manipulations that affect life span often have different magnitude of effect in males versus females. Moreover, the presence of a differentiated germ-line has been shown to affect life span in several species, including <it>Drosophila </it>and <it>C. elegans</it>.</p> <p>Methods</p> <p>Experiments were conducted to determine how alterations in sexual differentiation gene activity might affect the life span of <it>Drosophila melanogaster. Drosophila </it>females heterozygous for the <it>tudor[1]</it> mutation produce normal offspring, while their homozygous sisters produce offspring that lack a germ line. To identify additional sexual differentiation genes that might affect life span, the conditional transgenic system Geneswitch was employed, whereby feeding adult flies or developing larvae the drug RU486 causes the over-expression of selected UAS-transgenes.</p> <p>Results</p> <p>In this study germ-line ablation caused by the maternal <it>tudor[1]</it> mutation was examined in a long-lived genetic background, and was found to increase life span in males but not in females, consistent with previous reports. Fitting the data to a Gompertz-Makeham model indicated that the maternal <it>tudor[1]</it> mutation increases the life span of male progeny by decreasing age-independent mortality. The Geneswitch system was used to screen through several UAS-type and EP-type P element mutations in genes that regulate sexual differentiation, to determine if additional sex-specific effects on life span would be obtained. Conditional over-expression of <it>transformer </it>female isoform (<it>traF) </it>during development produced male adults with inhibited sexual differentiation, however this caused no significant change in life span. Over-expression of <it>doublesex </it>female isoform (<it>dsxF) </it>during development was lethal to males, and produced a limited number of female escapers, whereas over-expression of <it>dsxF </it>specifically in adults greatly reduced both male and female life span. Similarly, over-expression of <it>fruitless </it>male isoform <it>A </it>(<it>fru-MA</it>) during development was lethal to both males and females, whereas over-expression of <it>fru-MA </it>in adults greatly reduced both male and female life span.</p> <p>Conclusion</p> <p>Manipulation of sexual differentiation gene expression specifically in the adult, after morphological sexual differentiation is complete, was still able to affect life span. In addition, by manipulating gene expression during development, it was possible to significantly alter morphological sexual differentiation without a significant effect on adult life span. The data demonstrate that manipulation of sexual differentiation pathway genes either during development or in adults can affect adult life span.</p>http://www.biomedcentral.com/1471-2318/9/56 |
| spellingShingle | Tower John Landis Gary N Ford Daniel Shen Jie Identifying sexual differentiation genes that affect Drosophila life span BMC Geriatrics |
| title | Identifying sexual differentiation genes that affect Drosophila life span |
| title_full | Identifying sexual differentiation genes that affect Drosophila life span |
| title_fullStr | Identifying sexual differentiation genes that affect Drosophila life span |
| title_full_unstemmed | Identifying sexual differentiation genes that affect Drosophila life span |
| title_short | Identifying sexual differentiation genes that affect Drosophila life span |
| title_sort | identifying sexual differentiation genes that affect drosophila life span |
| url | http://www.biomedcentral.com/1471-2318/9/56 |
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