TY - GEN
T1 - Expression analysis of Jatropha curcas L. almt genes under low pH and aluminum stress
AU - Yuniati, Ratna
AU - Widyastuti, Utut
AU - Suharsono,
N1 - Publisher Copyright:
© 2016 Author(s).
PY - 2016/4/19
Y1 - 2016/4/19
N2 - In the previous study, the six populations of Jatropha curcas L. were grown on an acid Al-toxic subsoil (pH 4.3) media in the greenhouse and drained with nutrient solutions containing 3.2 mM AlCl3 to characterize their differences in response to Al toxicity. The Al treatment significantly affected all growth parameters. Statistical analysis on Al tolerance growth parameters showed a grouping pattern among the six Jatropha populations. They can be grouped into two clusters based on similar sensitivity to Al toxicity; those two groups represent the slightly tolerant and sensitive population to 3.2 mM AlCl3 following treatment for a month. Although grouped as Al-sensitive population, IP-2P has superior traits in productivity and those become the reason to use it as plant material to develop transgenic Jatropha plant. For the preliminary analysis, in this study IP-2P population was selected to subjected to gene expression analysis by qRT PCR. Quantitative real-time RT PCR analysis verified almt gene is preferentially expressed in the root tip, although transcript accumulate both in roots and leaves. Expression was highest at 24 h exposure rather than 7 days. Not all the transcripts are up-regulated by exposure to Al. Low pH (pH 4.0) treatment alone can also induce transcript accumulation both in the root apices and leaves but at significantly lower rates than observed for Al. In conclusion, it was found that Al stress in Jatropha root and leaf is not a specific response. Nonetheless, the Jatropha plants were relatively sensitive to Al stress. Therefore, this J. curcas L. IP-2P can be used for improving Al tolerance in plant by constructing transgenic plant carrying almt gene.
AB - In the previous study, the six populations of Jatropha curcas L. were grown on an acid Al-toxic subsoil (pH 4.3) media in the greenhouse and drained with nutrient solutions containing 3.2 mM AlCl3 to characterize their differences in response to Al toxicity. The Al treatment significantly affected all growth parameters. Statistical analysis on Al tolerance growth parameters showed a grouping pattern among the six Jatropha populations. They can be grouped into two clusters based on similar sensitivity to Al toxicity; those two groups represent the slightly tolerant and sensitive population to 3.2 mM AlCl3 following treatment for a month. Although grouped as Al-sensitive population, IP-2P has superior traits in productivity and those become the reason to use it as plant material to develop transgenic Jatropha plant. For the preliminary analysis, in this study IP-2P population was selected to subjected to gene expression analysis by qRT PCR. Quantitative real-time RT PCR analysis verified almt gene is preferentially expressed in the root tip, although transcript accumulate both in roots and leaves. Expression was highest at 24 h exposure rather than 7 days. Not all the transcripts are up-regulated by exposure to Al. Low pH (pH 4.0) treatment alone can also induce transcript accumulation both in the root apices and leaves but at significantly lower rates than observed for Al. In conclusion, it was found that Al stress in Jatropha root and leaf is not a specific response. Nonetheless, the Jatropha plants were relatively sensitive to Al stress. Therefore, this J. curcas L. IP-2P can be used for improving Al tolerance in plant by constructing transgenic plant carrying almt gene.
UR - http://www.scopus.com/inward/record.url?scp=84984592114&partnerID=8YFLogxK
U2 - 10.1063/1.4946965
DO - 10.1063/1.4946965
M3 - Conference contribution
AN - SCOPUS:84984592114
T3 - AIP Conference Proceedings
BT - International Symposium on Current Progress in Mathematics and Sciences 2015, ISCPMS 2015
A2 - Mart, Terry
A2 - Triyono, Djoko
PB - American Institute of Physics Inc.
T2 - 1st International Symposium on Current Progress in Mathematics and Sciences, ISCPMS 2015
Y2 - 3 November 2015 through 4 November 2015
ER -