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Gene discovery from Jatropha curcas by sequencing of ESTs from normalized and full-length enriched cDNA library from developing seeds

BACKGROUND: Jatropha curcas L. is promoted as an important non-edible biodiesel crop worldwide. Jatropha oil, which is a triacylglycerol, can be directly blended with petro-diesel or transesterified with methanol and used as biodiesel. Genetic improvement in jatropha is needed to increase the seed y...

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Autores principales: Natarajan, Purushothaman, Kanagasabapathy, Deepa, Gunadayalan, Gnanasekaran, Panchalingam, Jasintha, shree, Noopur, Sugantham, Priyanka Annabel, Singh, Kavita Kumari, Madasamy, Parani
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3091748/
https://www.ncbi.nlm.nih.gov/pubmed/20979643
http://dx.doi.org/10.1186/1471-2164-11-606
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author Natarajan, Purushothaman
Kanagasabapathy, Deepa
Gunadayalan, Gnanasekaran
Panchalingam, Jasintha
shree, Noopur
Sugantham, Priyanka Annabel
Singh, Kavita Kumari
Madasamy, Parani
author_facet Natarajan, Purushothaman
Kanagasabapathy, Deepa
Gunadayalan, Gnanasekaran
Panchalingam, Jasintha
shree, Noopur
Sugantham, Priyanka Annabel
Singh, Kavita Kumari
Madasamy, Parani
author_sort Natarajan, Purushothaman
collection PubMed
description BACKGROUND: Jatropha curcas L. is promoted as an important non-edible biodiesel crop worldwide. Jatropha oil, which is a triacylglycerol, can be directly blended with petro-diesel or transesterified with methanol and used as biodiesel. Genetic improvement in jatropha is needed to increase the seed yield, oil content, drought and pest resistance, and to modify oil composition so that it becomes a technically and economically preferred source for biodiesel production. However, genetic improvement efforts in jatropha could not take advantage of genetic engineering methods due to lack of cloned genes from this species. To overcome this hurdle, the current gene discovery project was initiated with an objective of isolating as many functional genes as possible from J. curcas by large scale sequencing of expressed sequence tags (ESTs). RESULTS: A normalized and full-length enriched cDNA library was constructed from developing seeds of J. curcas. The cDNA library contained about 1 × 10(6 )clones and average insert size of the clones was 2.1 kb. Totally 12,084 ESTs were sequenced to average high quality read length of 576 bp. Contig analysis revealed 2258 contigs and 4751 singletons. Contig size ranged from 2-23 and there were 7333 ESTs in the contigs. This resulted in 7009 unigenes which were annotated by BLASTX. It showed 3982 unigenes with significant similarity to known genes and 2836 unigenes with significant similarity to genes of unknown, hypothetical and putative proteins. The remaining 191 unigenes which did not show similarity with any genes in the public database may encode for unique genes. Functional classification revealed unigenes related to broad range of cellular, molecular and biological functions. Among the 7009 unigenes, 6233 unigenes were identified to be potential full-length genes. CONCLUSIONS: The high quality normalized cDNA library was constructed from developing seeds of J. curcas for the first time and 7009 unigenes coding for diverse biological functions including oil biosynthesis were identified. These genes will serve as invaluable genetic resource for crop improvement in jatropha to make it an ideal and profitable crop for biodiesel production.
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spelling pubmed-30917482011-05-11 Gene discovery from Jatropha curcas by sequencing of ESTs from normalized and full-length enriched cDNA library from developing seeds Natarajan, Purushothaman Kanagasabapathy, Deepa Gunadayalan, Gnanasekaran Panchalingam, Jasintha shree, Noopur Sugantham, Priyanka Annabel Singh, Kavita Kumari Madasamy, Parani BMC Genomics Research Article BACKGROUND: Jatropha curcas L. is promoted as an important non-edible biodiesel crop worldwide. Jatropha oil, which is a triacylglycerol, can be directly blended with petro-diesel or transesterified with methanol and used as biodiesel. Genetic improvement in jatropha is needed to increase the seed yield, oil content, drought and pest resistance, and to modify oil composition so that it becomes a technically and economically preferred source for biodiesel production. However, genetic improvement efforts in jatropha could not take advantage of genetic engineering methods due to lack of cloned genes from this species. To overcome this hurdle, the current gene discovery project was initiated with an objective of isolating as many functional genes as possible from J. curcas by large scale sequencing of expressed sequence tags (ESTs). RESULTS: A normalized and full-length enriched cDNA library was constructed from developing seeds of J. curcas. The cDNA library contained about 1 × 10(6 )clones and average insert size of the clones was 2.1 kb. Totally 12,084 ESTs were sequenced to average high quality read length of 576 bp. Contig analysis revealed 2258 contigs and 4751 singletons. Contig size ranged from 2-23 and there were 7333 ESTs in the contigs. This resulted in 7009 unigenes which were annotated by BLASTX. It showed 3982 unigenes with significant similarity to known genes and 2836 unigenes with significant similarity to genes of unknown, hypothetical and putative proteins. The remaining 191 unigenes which did not show similarity with any genes in the public database may encode for unique genes. Functional classification revealed unigenes related to broad range of cellular, molecular and biological functions. Among the 7009 unigenes, 6233 unigenes were identified to be potential full-length genes. CONCLUSIONS: The high quality normalized cDNA library was constructed from developing seeds of J. curcas for the first time and 7009 unigenes coding for diverse biological functions including oil biosynthesis were identified. These genes will serve as invaluable genetic resource for crop improvement in jatropha to make it an ideal and profitable crop for biodiesel production. BioMed Central 2010-10-27 /pmc/articles/PMC3091748/ /pubmed/20979643 http://dx.doi.org/10.1186/1471-2164-11-606 Text en Copyright ©2010 Natarajan et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Natarajan, Purushothaman
Kanagasabapathy, Deepa
Gunadayalan, Gnanasekaran
Panchalingam, Jasintha
shree, Noopur
Sugantham, Priyanka Annabel
Singh, Kavita Kumari
Madasamy, Parani
Gene discovery from Jatropha curcas by sequencing of ESTs from normalized and full-length enriched cDNA library from developing seeds
title Gene discovery from Jatropha curcas by sequencing of ESTs from normalized and full-length enriched cDNA library from developing seeds
title_full Gene discovery from Jatropha curcas by sequencing of ESTs from normalized and full-length enriched cDNA library from developing seeds
title_fullStr Gene discovery from Jatropha curcas by sequencing of ESTs from normalized and full-length enriched cDNA library from developing seeds
title_full_unstemmed Gene discovery from Jatropha curcas by sequencing of ESTs from normalized and full-length enriched cDNA library from developing seeds
title_short Gene discovery from Jatropha curcas by sequencing of ESTs from normalized and full-length enriched cDNA library from developing seeds
title_sort gene discovery from jatropha curcas by sequencing of ests from normalized and full-length enriched cdna library from developing seeds
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3091748/
https://www.ncbi.nlm.nih.gov/pubmed/20979643
http://dx.doi.org/10.1186/1471-2164-11-606
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