Maize Haploid Induction Gene and Marker-Assisted Breeding

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Solution Overview

Problem

Current methods for establishing homozygous lines in maize breeding are time-consuming, and existing inducer lines for haploid induction in maize have limitations such as poor pollen efficiency, requiring lengthy and costly processes for breeding and seed multiplication, with a need for improved molecular markers for haploid induction.

Innovation Solution

Identification of a gene homologous to the acyl transferase/acyl hydrolase/lysophospholipase family responsible for haploid induction in maize, along with associated molecular markers, which enables the development of polynucleotides and recombinant DNA constructs to enhance haploid induction efficiency and streamline breeding processes.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If traditional methods are used to establish homozygous lines, then genetic stability is achieved, but the time required is excessively long (8-10 generations)

Engineering Contradiction:
Improvegenetic stabilityVSAvoidtime for obtaining homozygous lines
Core Design Contradiction:
ReliabilityVSLoss of time

Solution Approach 1:

The patent applies preliminary action by inducing haploids at an early stage (F1 generation) through crossing with inducer lines, rather than waiting for traditional multi-generation selfing. This allows homozygous lines to be obtained in just 2-3 generations by doubling chromosomes in the haploid stage, dramatically reducing the time from 8-10 generations to 2-3 generations while maintaining genetic stability

Inventive Principle:
Principle #10Preliminary action

2Productivity

If existing inducer lines are used for haploid induction, then haploid production is achieved, but pollen efficiency is poor and processes are lengthy and costly

Engineering Contradiction:
Improvehaploid induction abilityVSAvoidbreeding and seed multiplication process
Core Design Contradiction:
ProductivityVSEase of manufacture

Solution Approach 1:

The patent applies parameter changes by modifying the inducer line genetics through marker-assisted selection. Specific molecular markers (umc1917, bnlg1811, and others) are used to identify and select lines with enhanced haploid induction ability, changing the genetic parameters of the inducer lines to improve pollen efficiency and reduce the complexity of breeding processes

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent replaces mechanical/phenotypic selection methods with molecular marker-based selection. Instead of relying on time-consuming phenotypic evaluation of haploid induction ability, the invention uses DNA markers to directly identify lines with the desired trait, substituting a faster, more precise molecular detection system for traditional mechanical selection processes

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

3Measurement precision

If molecular markers are used for allele identification, then selection precision is improved, but the complexity of the process increases

Engineering Contradiction:
Improveallele identification accuracyVSAvoidmolecular marker screening process
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent applies universality by developing a standardized molecular marker system that can be applied across multiple inducer line development projects. The markers (umc1917, bnlg1811, and others) serve multiple functions: identifying haploid induction ability, tracking allele inheritance, and selecting superior lines, thereby reducing overall process complexity despite the added precision

Inventive Principle:
Principle #6Universality (Multi-functionality)

Data Source

PatentEP3292204B1Polynucleotide responsible of haploid induction in maize plants and related processes
Publication Date: 2023.06.28 LIMAGRAIN EURO SA
  • EP3292204B1 patent drawingFigure 1
  • EP3292204B1 patent drawingFigure 2
  • EP3292204B1 patent drawingFigure 2

AI summary

The present invention concerns an isolated polynucleotide responsible of haploid induction in maize plants and related processes. Additionally, the invention relates to plants that have been genetically transformed with the polynucleotide of the invention. The invention also relates to a process for screening a mutant plant population for enhanced haploid induction by using said isolated polynucleotide. The invention further relates to molecular markers associated with haploid induction in maize plants and their use in quality control for inducer lines.