# A Review of Research Progress in Rice Anther Culture

**Authors:** Zhizun Feng, Huangwei Chu, Liming Cao, Ruiyun Wang, Anpeng Zhang

PMC · DOI: 10.3390/cimb48010018 · Current Issues in Molecular Biology · 2025-12-24

## TL;DR

This paper reviews the progress of rice anther culture, a technique that accelerates rice breeding by producing stable lines in one generation.

## Contribution

The paper provides a comprehensive review of rice anther culture's development, mechanisms, and future directions.

## Key findings

- Anther culture is the primary method for obtaining haploids in rice breeding.
- Efficient haploid induction is crucial for successful haploid breeding.
- Factors affecting anther culture efficiency and their genetic mechanisms are discussed.

## Abstract

Conventional rice breeding predominantly relies on hybridization techniques, with hybrid progenies typically requiring 8 to 10 generations of selfing to achieve genetically stable homozygous lines. In contrast, haploid breeding enables the derivation of stable doubled haploid (DH) lines from hybrid progeny in just one generation, substantially shortening the breeding cycle. Haploid breeding comprises two core steps: haploid induction and chromosome doubling, with efficient haploid induction being pivotal to the success of this technology. Currently, anther culture, due to its relatively mature and stable protocol, has become the primary method for obtaining haploids in rice haploid breeding. This review systematically summarizes the research progress in rice anther culture, focusing on the fundamental steps and applications of haploid breeding, the developmental history of anther culture, factors influencing anther culture efficiency and their underlying genetic mechanisms, current challenges and potential countermeasures, and future prospects for rice anther culture technology.

## Full text

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## Figures

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## References

72 references — full list in the complete paper: https://tomesphere.com/paper/PMC12839740/full.md

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Source: https://tomesphere.com/paper/PMC12839740