Constructing a New Integrated Genetic Linkage Map and Mapping Quantitative Trait Loci for Vegetative Mycelium Growth Rate in Lentinula edodes

Summary

This research created the most detailed genetic map of shiitake mushroom to date, helping identify specific genetic regions that control how fast the mushroom grows. This has important practical applications for mushroom cultivation and breeding. Impacts on everyday life: • Better understanding of mushroom genetics can lead to faster-growing shiitake strains • Improved mushroom breeding could result in higher yields for farmers and lower costs for consumers • More efficient cultivation methods could make shiitake mushrooms more widely available • Enhanced breeding techniques could lead to more disease-resistant mushroom varieties • The findings could help develop more sustainable mushroom farming practices

Background

Lentinula edodes (shiitake) is one of the most widely cultivated edible mushrooms globally, particularly in East Asia. It has important culinary, medicinal, and biotechnological applications, including antitumor and antiviral properties. The fungus possesses a powerful ligninolytic enzyme system with potential for bioconversion of lignocellulosic wastes. Previous genetic maps had limitations in population size and marker density, necessitating a higher quality map for better QTL mapping.

Objective

The study aimed to construct a high-quality genetic linkage map for Lentinula edodes and detect quantitative trait loci (QTLs) controlling vegetative growth rate. The researchers sought to develop a more saturated linkage map based on a larger mapping population and more markers than previous studies, while also analyzing growth rates on various synthetic media.

Results

The constructed genetic map spanned 1006.1 cM with an average marker spacing of 2.0 cM. Two QTLs were identified in the monokaryotic population and 13 putative QTLs in two testcross dikaryotic populations, mapped across seven different linkage groups. Several growth rate-related QTLs were clustered on LG4 and LG6. The QTL hotspot on LG4 was found near the mating-type A locus. The QTL Qdgr2 on LG4 was detected across different media, contributing 8.07-23.71% of phenotypic variation.

Conclusion

The study produced the most saturated linkage map of L. edodes to date, providing essential information for QTL mapping and marker-assisted selection. The identification of QTL clusters controlling mycelium growth rate, particularly on LG4 and LG6, reveals main genomic areas responsible for growth regulation and control.
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