Gene expression studies using a miniaturized thermal cycler system on board the International Space Station.
The distance and duration of human spaceflight missions is set to markedly increase over the coming decade as we prepare to send astronauts to Mars. However, the health impact of long-term exposure to cosmic radiation and microgravity is not fully understood. In order to identify the molecular mecha...
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doaj-d8d7598363d74cd0ada589cf14771fe22020-11-25T00:08:50ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-011310e020585210.1371/journal.pone.0205852Gene expression studies using a miniaturized thermal cycler system on board the International Space Station.Tessa G MontagueAlia AlmansooriEmily J GleasonD Scott CopelandKevin FoleySebastian KravesEzequiel Alvarez SaavedraThe distance and duration of human spaceflight missions is set to markedly increase over the coming decade as we prepare to send astronauts to Mars. However, the health impact of long-term exposure to cosmic radiation and microgravity is not fully understood. In order to identify the molecular mechanisms underpinning the effects of space travel on human health, we must develop the capacity to monitor changes in gene expression and DNA integrity in space. Here, we report successful implementation of three molecular biology procedures on board the International Space Station (ISS) using a miniaturized thermal cycler system and C. elegans as a model organism: first, DNA extraction-the initial step for any type of DNA analysis; second, reverse transcription of RNA to generate complementary DNA (cDNA); and third, the subsequent semi-quantitative PCR amplification of cDNA to analyze gene expression changes in space. These molecular procedures represent a significant expansion of the budding molecular biology capabilities of the ISS and will permit more complex analyses of space-induced genetic changes during spaceflight missions aboard the ISS and beyond.http://europepmc.org/articles/PMC6209215?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Tessa G Montague Alia Almansoori Emily J Gleason D Scott Copeland Kevin Foley Sebastian Kraves Ezequiel Alvarez Saavedra |
spellingShingle |
Tessa G Montague Alia Almansoori Emily J Gleason D Scott Copeland Kevin Foley Sebastian Kraves Ezequiel Alvarez Saavedra Gene expression studies using a miniaturized thermal cycler system on board the International Space Station. PLoS ONE |
author_facet |
Tessa G Montague Alia Almansoori Emily J Gleason D Scott Copeland Kevin Foley Sebastian Kraves Ezequiel Alvarez Saavedra |
author_sort |
Tessa G Montague |
title |
Gene expression studies using a miniaturized thermal cycler system on board the International Space Station. |
title_short |
Gene expression studies using a miniaturized thermal cycler system on board the International Space Station. |
title_full |
Gene expression studies using a miniaturized thermal cycler system on board the International Space Station. |
title_fullStr |
Gene expression studies using a miniaturized thermal cycler system on board the International Space Station. |
title_full_unstemmed |
Gene expression studies using a miniaturized thermal cycler system on board the International Space Station. |
title_sort |
gene expression studies using a miniaturized thermal cycler system on board the international space station. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2018-01-01 |
description |
The distance and duration of human spaceflight missions is set to markedly increase over the coming decade as we prepare to send astronauts to Mars. However, the health impact of long-term exposure to cosmic radiation and microgravity is not fully understood. In order to identify the molecular mechanisms underpinning the effects of space travel on human health, we must develop the capacity to monitor changes in gene expression and DNA integrity in space. Here, we report successful implementation of three molecular biology procedures on board the International Space Station (ISS) using a miniaturized thermal cycler system and C. elegans as a model organism: first, DNA extraction-the initial step for any type of DNA analysis; second, reverse transcription of RNA to generate complementary DNA (cDNA); and third, the subsequent semi-quantitative PCR amplification of cDNA to analyze gene expression changes in space. These molecular procedures represent a significant expansion of the budding molecular biology capabilities of the ISS and will permit more complex analyses of space-induced genetic changes during spaceflight missions aboard the ISS and beyond. |
url |
http://europepmc.org/articles/PMC6209215?pdf=render |
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