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Two Arabidopsis promoters drive seed-coat specific gene expression in pennycress and camelina.


ABSTRACT:

Background

Pennycress and camelina are two important novel biofuel oilseed crop species. Their seeds contain high content of oil that can be easily converted into biodiesel or jet fuel, while the left-over materials are usually made into press cake meals for feeding livestock. Therefore, the ability to manipulate the seed coat encapsulating the oil- and protein-rich embryos is critical for improving seed oil production and press cake quality.

Results

Here, we tested the promoter activity of two Arabidopsis seed coat genes, AtTT10 and AtDP1, in pennycress and camelina by using eGFP and GUS reporters. Overall, both promoters show high levels of activities in the seed coat in these two biofuel crops, with very low or no expression in other tissues. Importantly, AtTT10 promoter activity in camelina shows differences from that in Arabidopsis, which highlights that the behavior of an exogenous promoter in closely related species cannot be assumed the same and still requires experimental determination.

Conclusion

Our work demonstrates that AtTT10 and AtDP1 promoters are suitable for driving gene expression in the outer integument of the seed coat in pennycress and camelina.

SUBMITTER: Li X 

PROVIDER: S-EPMC10699083 | biostudies-literature | 2023 Dec

REPOSITORIES: biostudies-literature

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Two Arabidopsis promoters drive seed-coat specific gene expression in pennycress and camelina.

Li Xin X   Yell Victoria V   Li Xu X  

Plant methods 20231206 1


<h4>Background</h4>Pennycress and camelina are two important novel biofuel oilseed crop species. Their seeds contain high content of oil that can be easily converted into biodiesel or jet fuel, while the left-over materials are usually made into press cake meals for feeding livestock. Therefore, the ability to manipulate the seed coat encapsulating the oil- and protein-rich embryos is critical for improving seed oil production and press cake quality.<h4>Results</h4>Here, we tested the promoter a  ...[more]

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