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Characterization of LpGPAT Gene in Lilium pensylvanicum and Response to Cold Stress
LpGPAT was obtained from L. pensylvanicum using RT-PCR and rapid amplification of cDNA ends. The cloned full-length cDNA was 1544 bp; it encoded 410 amino acids and had a molecular size of 46 KDa. The nucleic acid sequence analysis showed that it shared high homology with other known GPATs. SMAT res...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4331407/ https://www.ncbi.nlm.nih.gov/pubmed/25710023 http://dx.doi.org/10.1155/2015/792819 |
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author | Sun, Shao-kun Yang, Ni-na Chen, Li-jing Irfan, Muhammad Zhao, Xing-hua Li, Tian-lai |
author_facet | Sun, Shao-kun Yang, Ni-na Chen, Li-jing Irfan, Muhammad Zhao, Xing-hua Li, Tian-lai |
author_sort | Sun, Shao-kun |
collection | PubMed |
description | LpGPAT was obtained from L. pensylvanicum using RT-PCR and rapid amplification of cDNA ends. The cloned full-length cDNA was 1544 bp; it encoded 410 amino acids and had a molecular size of 46 KDa. The nucleic acid sequence analysis showed that it shared high homology with other known GPATs. SMAT result suggests that there is a PlsC that exists in 176-322 amino acid sequence of LpGAPT; it means LpGPAT protein is a member of the family of acyltransferase and has acyltransferase enzymatic activity. Result of real-time quantitative PCR and semiquantitative PCR support LpGPAT gene is definitely induced by low temperature stress. |
format | Online Article Text |
id | pubmed-4331407 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-43314072015-02-23 Characterization of LpGPAT Gene in Lilium pensylvanicum and Response to Cold Stress Sun, Shao-kun Yang, Ni-na Chen, Li-jing Irfan, Muhammad Zhao, Xing-hua Li, Tian-lai Biomed Res Int Research Article LpGPAT was obtained from L. pensylvanicum using RT-PCR and rapid amplification of cDNA ends. The cloned full-length cDNA was 1544 bp; it encoded 410 amino acids and had a molecular size of 46 KDa. The nucleic acid sequence analysis showed that it shared high homology with other known GPATs. SMAT result suggests that there is a PlsC that exists in 176-322 amino acid sequence of LpGAPT; it means LpGPAT protein is a member of the family of acyltransferase and has acyltransferase enzymatic activity. Result of real-time quantitative PCR and semiquantitative PCR support LpGPAT gene is definitely induced by low temperature stress. Hindawi Publishing Corporation 2015 2015-02-01 /pmc/articles/PMC4331407/ /pubmed/25710023 http://dx.doi.org/10.1155/2015/792819 Text en Copyright © 2015 Shao-kun Sun et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Sun, Shao-kun Yang, Ni-na Chen, Li-jing Irfan, Muhammad Zhao, Xing-hua Li, Tian-lai Characterization of LpGPAT Gene in Lilium pensylvanicum and Response to Cold Stress |
title | Characterization of LpGPAT Gene in Lilium pensylvanicum and Response to Cold Stress |
title_full | Characterization of LpGPAT Gene in Lilium pensylvanicum and Response to Cold Stress |
title_fullStr | Characterization of LpGPAT Gene in Lilium pensylvanicum and Response to Cold Stress |
title_full_unstemmed | Characterization of LpGPAT Gene in Lilium pensylvanicum and Response to Cold Stress |
title_short | Characterization of LpGPAT Gene in Lilium pensylvanicum and Response to Cold Stress |
title_sort | characterization of lpgpat gene in lilium pensylvanicum and response to cold stress |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4331407/ https://www.ncbi.nlm.nih.gov/pubmed/25710023 http://dx.doi.org/10.1155/2015/792819 |
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