Identification of laticifer-specific genes and their promoter regions from a natural rubber producing plant Hevea brasiliensis
Latex, the milky cytoplasm of highly differentiated cells called laticifers, from Hevea brasiliensis is a key source of commercial natural rubber production. One way to enhance natural rubber production would be to express genes involved in natural rubber biosynthesis by a laticifer-specific overexp...
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th-mahidol.331622018-11-09T09:00:47Z Identification of laticifer-specific genes and their promoter regions from a natural rubber producing plant Hevea brasiliensis Yuichi Aoki Seiji Takahashi Daisuke Takayama Yoshiyuki Ogata Nozomu Sakurai Hideyuki Suzuki Kasem Asawatreratanakul Dhirayos Wititsuwannakul Rapepun Wititsuwannakul Daisuke Shibata Tanetoshi Koyama Toru Nakayama Tohoku University Kazusa DNA Research Institute Thaksin University Mahidol University Prince of Songkla University Osaka Prefecture University Agricultural and Biological Sciences Biochemistry, Genetics and Molecular Biology Latex, the milky cytoplasm of highly differentiated cells called laticifers, from Hevea brasiliensis is a key source of commercial natural rubber production. One way to enhance natural rubber production would be to express genes involved in natural rubber biosynthesis by a laticifer-specific overexpression system. As a first step to identify promoters which could regulate the laticifer-specific expression, we identified random clones from a cDNA library of H. brasiliensis latex, resulting in 4325 expressed sequence tags (ESTs) assembled into 1308 unigenes (692 contigs and 617 singletons). Quantitative analyses of the transcription levels of high redundancy clones in the ESTs revealed genes highly and predominantly expressed in laticifers, such as Rubber Elongation Factor (REF), Small Rubber Particle Protein and putative protease inhibitor proteins. HRT1 and HRT2, cis-prenyltransferases involved in rubber biosynthesis, was also expressed predominantly in laticifers, although these transcript levels were 80-fold lower than that of REF. The 5'-upstream regions of these laticifer-specific genes were cloned and analyzed in silico, revealing seven common motifs consisting of eight bases. Furthermore, transcription factors specifically expressed in laticifers were also identified. The common motifs in the laticifer-specific genes and the laticifer-specific transcription factors are potentially involved in the regulation of gene expression in laticifers. © 2014 Elsevier Ireland Ltd. 2018-11-09T01:48:23Z 2018-11-09T01:48:23Z 2014-01-01 Article Plant Science. Vol.225, (2014), 1-8 10.1016/j.plantsci.2014.05.003 01689452 2-s2.0-84901585475 https://repository.li.mahidol.ac.th/handle/123456789/33162 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84901585475&origin=inward |
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Agricultural and Biological Sciences Biochemistry, Genetics and Molecular Biology Yuichi Aoki Seiji Takahashi Daisuke Takayama Yoshiyuki Ogata Nozomu Sakurai Hideyuki Suzuki Kasem Asawatreratanakul Dhirayos Wititsuwannakul Rapepun Wititsuwannakul Daisuke Shibata Tanetoshi Koyama Toru Nakayama Identification of laticifer-specific genes and their promoter regions from a natural rubber producing plant Hevea brasiliensis |
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Latex, the milky cytoplasm of highly differentiated cells called laticifers, from Hevea brasiliensis is a key source of commercial natural rubber production. One way to enhance natural rubber production would be to express genes involved in natural rubber biosynthesis by a laticifer-specific overexpression system. As a first step to identify promoters which could regulate the laticifer-specific expression, we identified random clones from a cDNA library of H. brasiliensis latex, resulting in 4325 expressed sequence tags (ESTs) assembled into 1308 unigenes (692 contigs and 617 singletons). Quantitative analyses of the transcription levels of high redundancy clones in the ESTs revealed genes highly and predominantly expressed in laticifers, such as Rubber Elongation Factor (REF), Small Rubber Particle Protein and putative protease inhibitor proteins. HRT1 and HRT2, cis-prenyltransferases involved in rubber biosynthesis, was also expressed predominantly in laticifers, although these transcript levels were 80-fold lower than that of REF. The 5'-upstream regions of these laticifer-specific genes were cloned and analyzed in silico, revealing seven common motifs consisting of eight bases. Furthermore, transcription factors specifically expressed in laticifers were also identified. The common motifs in the laticifer-specific genes and the laticifer-specific transcription factors are potentially involved in the regulation of gene expression in laticifers. © 2014 Elsevier Ireland Ltd. |
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Tohoku University |
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Tohoku University Yuichi Aoki Seiji Takahashi Daisuke Takayama Yoshiyuki Ogata Nozomu Sakurai Hideyuki Suzuki Kasem Asawatreratanakul Dhirayos Wititsuwannakul Rapepun Wititsuwannakul Daisuke Shibata Tanetoshi Koyama Toru Nakayama |
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Article |
author |
Yuichi Aoki Seiji Takahashi Daisuke Takayama Yoshiyuki Ogata Nozomu Sakurai Hideyuki Suzuki Kasem Asawatreratanakul Dhirayos Wititsuwannakul Rapepun Wititsuwannakul Daisuke Shibata Tanetoshi Koyama Toru Nakayama |
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Yuichi Aoki |
title |
Identification of laticifer-specific genes and their promoter regions from a natural rubber producing plant Hevea brasiliensis |
title_short |
Identification of laticifer-specific genes and their promoter regions from a natural rubber producing plant Hevea brasiliensis |
title_full |
Identification of laticifer-specific genes and their promoter regions from a natural rubber producing plant Hevea brasiliensis |
title_fullStr |
Identification of laticifer-specific genes and their promoter regions from a natural rubber producing plant Hevea brasiliensis |
title_full_unstemmed |
Identification of laticifer-specific genes and their promoter regions from a natural rubber producing plant Hevea brasiliensis |
title_sort |
identification of laticifer-specific genes and their promoter regions from a natural rubber producing plant hevea brasiliensis |
publishDate |
2018 |
url |
https://repository.li.mahidol.ac.th/handle/123456789/33162 |
_version_ |
1763490153914957824 |