BRRV Promoter Tissue-Preferred Expression in Plants

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Solution Overview

Problem

Current plant genetic engineering techniques face challenges in site-specific regulation of gene expression, particularly in directing the synthesis of desirable proteins or compounds to specific tissues to maximize commercial applications, such as producing pathogen-resistant traits without affecting edible tissues.

Innovation Solution

Development of novel nucleotide sequences derived from a blueberry red ringspot virus (BRRV) isolate, including a full-length, truncated, and duplicated promoter, which drives constitutive expression and tissue-preferred expression in plants, allowing for the modulation of gene expression in selected tissues.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If constitutive promoters are used to drive continuous gene expression throughout plant cells, then productivity is improved, but the ability to direct expression to specific tissues is lost

Engineering Contradiction:
Improvegene expression levelVSAvoidtissue-specific regulation
Core Design Contradiction:
ProductivityVSEase of operation

Solution Approach 1:

The patent applies local quality by creating promoters with tissue-preferred expression capabilities. The BRRV promoter variants are engineered to drive high-level expression specifically in green tissues (leaves, stems) while minimizing expression in non-green tissues (roots, flowers). This allows the expression system to have different expression characteristics in different tissue locations, resolving the contradiction between continuous expression and tissue-specific regulation.

Inventive Principle:
Principle #3Local quality

2Manufacturing precision

If tissue-preferred promoters are used to direct expression to specific tissues, then manufacturing precision is improved, but overall productivity decreases

Engineering Contradiction:
Improvetissue-specific expression controlVSAvoidtotal gene expression level
Core Design Contradiction:
Manufacturing precisionVSProductivity

Solution Approach 1:

The patent employs parameter changes by modifying the BRRV promoter sequence to create variants with enhanced green tissue preference. Through truncation and duplication of specific promoter regions, the expression pattern parameter is optimized to concentrate expression in green tissues while maintaining high expression levels. This allows simultaneous achievement of tissue-specific precision and high productivity within the target tissue compartment.

Inventive Principle:
Principle #35Parameter changes

3Reliability

If inducible promoters are used to activate transcription in response to pathogens, then reliability of pathogen defense is improved, but response time and complexity increase

Engineering Contradiction:
Improvepathogen defense effectivenessVSAvoidregulatory mechanism complexity
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent applies self-service by utilizing the plant's own green tissue identity and metabolic activity to drive promoter expression. The BRRV promoter variants automatically activate expression in green tissues through intrinsic regulatory elements that respond to plant physiological states rather than requiring external pathogen induction. This simplifies the regulatory mechanism while maintaining reliable expression in the desired tissue compartment where pathogen defense is most needed.

Inventive Principle:
Principle #25Self-service

Data Source

PatentUS8895716B2Viral promoter, truncations thereof, and methods of use
Publication Date: 2014.11.25 PIONEER HI BREED INTERNATIONAL INC
  • US8895716B2 patent drawing
  • US8895716B2 patent drawing

AI summary

The present disclosure provides compositions and methods for regulating expression of heterologous nucleotide sequences in a plant. Compositions include a novel nucleotide sequence for a promoter. A method for expressing a heterologous nucleotide sequence in a plant using the promoter sequence disclosed herein is provided. The method comprises stably incorporating into the genome of a plant cell a nucleotide sequence operably linked to the promoter of the present invention and regenerating a stably transformed plant that expresses the nucleotide sequence.