Difference between revisions of "Os02g0510200"
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===Expression=== | ===Expression=== | ||
In order to determine whether the stable integration of the transgenes occurred in the rice genome, Southern blot analysis was performed using a probe containing a 502-bp fragment consisting of the coding region of the OsmALS gene (Fig. 1). Since OsmALS and wild-type OsALS sequences are distinguished only by two substitutions, the original band of wild-type OsALS is seen at around 3 kb in all plants including non-transformants (Fig. 7). | In order to determine whether the stable integration of the transgenes occurred in the rice genome, Southern blot analysis was performed using a probe containing a 502-bp fragment consisting of the coding region of the OsmALS gene (Fig. 1). Since OsmALS and wild-type OsALS sequences are distinguished only by two substitutions, the original band of wild-type OsALS is seen at around 3 kb in all plants including non-transformants (Fig. 7). | ||
| + | [[File:5-f7.png |center |thumb |10000px |''''''Fig. 7 Southern blot analysis of BS-resistant plants (T0 generation).The blot was probed with a 502-bp fragment consisting of the coding region of the OsmALS gene (Fig. 1). Arrows indicate the wild-type ALS gene. Lanes 1–25, transgenic plants regenerated from BS-resistant calli of each cultivar; Lanes N, non-transformants of each cultivar'''''']] | ||
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===Evolution=== | ===Evolution=== | ||
Please input evolution information here. | Please input evolution information here. | ||
Revision as of 03:31, 29 July 2016
Bispyribac sodium (BS), a pyrimidinyl carboxy herbicide, is a well-known inhibitor of acetolactate synthase (ALS) activity. ALS is an enzyme in the biosynthetic pathway for branched-chain amino acids.
Contents
Annotated Information
Function
Bispyribac sodium (BS), a pyrimidinyl carboxy herbicide, is a well-known inhibitor of acetolactate synthase (ALS) activity. ALS is an enzyme in the biosynthetic pathway for branched-chain amino acids. BS can be used with OsmALS [W548L/S627I] to select transformed cells, and that this method is suitable for obtaining transgenic indica and indica-derived rice cultivars.
Expression
In order to determine whether the stable integration of the transgenes occurred in the rice genome, Southern blot analysis was performed using a probe containing a 502-bp fragment consisting of the coding region of the OsmALS gene (Fig. 1). Since OsmALS and wild-type OsALS sequences are distinguished only by two substitutions, the original band of wild-type OsALS is seen at around 3 kb in all plants including non-transformants (Fig. 7).
Evolution
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Labs working on this gene
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References
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