Sugarcane bacilliform viral (SCBV) enhancer and its use in plant functional genomics
Identification of new enhancer sequence has significant utility in the plant functional genomics. The sugarcane bacilliform badnavirus (SCBV) transcriptional enhancer has been identified. This enhancer can be used to increase the rate of transcription from gene promoters and in activation tagging experiments. A ten-fold increase in transcription was observed when a 4× array of the SCBV enhancer was placed upstream of a truncated form of the maize alcohol dehydrogenase minimal promoter. Methods of using the SCBV transcriptional enhancer are described, as are chimeric transcription regulatory regions, constructs, cells, tissues, and organisms that comprise one or more copies of the enhancer.
1. A plant tissue comprising a sugarcane bacilliform virus (SCBV) construct said construct comprising
(i) one or more SCBV enhancer elements consisting essentially of position 337 to position 618 of SEQ ID NO: 1; (ii) a plant promoter heterologous to said enhancer elements wherein said plant promoter comprises an RNA polymerase binding site and a mRNA initiation site; and
(iii) an expression sequence,
wherein the one or more SCBV enhancer elements, the heterologous plant promoter, and the expression sequence are operably linked thereby forming a SCBV construct and wherein each of said one or more SCBV enhancer elements lack an SCBV promoter sequence from positions 619 to 839 of SEQ ID NO: 1.
2. The plant tissue of claim 1 , wherein the expression sequence comprises a marker gene.
3. The plant tissue of claim 1 , wherein the expression sequence comprises a gene of agronomic interest.
4. The plant tissue of claim 1 , wherein the heterologous plant promoter is a maize ubiquitin promoter, a maize alcohol dehydrogenase 1 (Adhl) promoter or a rice actin promoter.
5. A method of making transgenic plant tissue comprising a sugarcane bacilliform virus (SCBV) construct comprising
transforming plant tissue with a polynucleotide comprising an SCBV construct comprising (i) one or more SCBV enhancer elements consisting essentially of position 337 to position 618 of SEQ ID NO: 1, (ii) a plant promoter sequence heterologous to said enhancer elements wherein said plant promoter comprises an RNA polymerase binding site and an mRNA initiation site, and (iii) an expression sequence,
wherein the one or more SCBV enhancer elements, the heterologous promoter sequence, and the expression sequence are operably linked thereby forming an SCBV construct and wherein each of said one or more SCBV enhancer elements lack an SCBV promoter sequence from positions 619 to 839 of SEQ ID NO: 1.
6. The method of claims 5 , further comprising evaluating an expression profile of the expression sequence in the plant tissue.
7. The method of claim 5 , further comprising culturing the plant tissue to create a transgenic plant comprising the SCBV construct.
8. The method of claim 7 , further comprising evaluating the expression level of the expression sequence in the plant.
9. The method of claim 5 , wherein the expression sequence comprises a marker gene.
10. The method of claim 5 , wherein the expression sequence comprises a gene of agronomic interest.
11. The method of claim 5 , wherein the heterologous plant promoter is a maize ubiquitin promoter, a maize alcohol dehydrogenase 1 (Adh1) promoter or a rice actin promoter.
12. The plant tissue of claim 1 , wherein the SCBV construct comprises two or more SCBV enhancer elements each consisting essentially of position 337 to position 618 of SEQ ID NO: 1.
13. The plant tissue of claim 1 , wherein the SCBV construct comprises four SCBV enhancer elements, each consisting essentially of position 337 to position 618 of SEQ ID NO:1.
14. The method of claim 5 , wherein the SCBV construct comprises two or more SCBV enhancer elements each consisting essentially of position 337 to position 618 of SEQ ID NO: 1.
15. The plant tissue of claim 5 , wherein the SCBV construct comprises four SCBV enhancer elements, each consisting essentially of position 337 to position 618 of SEQ ID NO: 1.