Autor: |
Tung Shu-Yun, Chou Shu-Jen, Shen Shu-Chen, Liu Nien-Tze, Wu Fu-Hui, Liao De-Chih, Hsu Chen-Tran, Yang Chang-Hsien, Chan Ming-Tsair, Lin Choun-Sea |
Jazyk: |
angličtina |
Rok vydání: |
2011 |
Předmět: |
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Zdroj: |
BMC Plant Biology, Vol 11, Iss 1, p 60 (2011) |
Druh dokumentu: |
article |
ISSN: |
1471-2229 |
DOI: |
10.1186/1471-2229-11-60 |
Popis: |
Abstract Background Orchids comprise one of the largest families of flowering plants and generate commercially important flowers. However, model plants, such as Arabidopsis thaliana do not contain all plant genes, and agronomic and horticulturally important genera and species must be individually studied. Results Several molecular biology tools were used to isolate flower-specific gene promoters from Oncidium 'Gower Ramsey' (Onc. GR). A cDNA library of reproductive tissues was used to construct a microarray in order to compare gene expression in flowers and leaves. Five genes were highly expressed in flower tissues, and the subcellular locations of the corresponding proteins were identified using lip transient transformation with fluorescent protein-fusion constructs. BAC clones of the 5 genes, together with 7 previously published flower- and reproductive growth-specific genes in Onc. GR, were identified for cloning of their promoter regions. Interestingly, 3 of the 5 novel flower-abundant genes were putative trypsin inhibitor (TI) genes (OnTI1, OnTI2 and OnTI3), which were tandemly duplicated in the same BAC clone. Their promoters were identified using transient GUS reporter gene transformation and stable A. thaliana transformation analyses. Conclusions By combining cDNA microarray, BAC library, and bombardment assay techniques, we successfully identified flower-directed orchid genes and promoters. |
Databáze: |
Directory of Open Access Journals |
Externí odkaz: |
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