Transcriptome analysis and development of EST-SSR markers in the mushroom Auricularia heimuer

• Published in: Scientific reports 2024-05, Vol.14 (1), p.12340-10, Article 12340
• Main Authors: Jiao, Lihe, Han, Chuang, Zhu, Jianan, Zhang, Piqi, Ma, Yinpeng, Dai, Xiaodong, Zhang, Yunzhi
• Format: Article
• Language: English
• Subjects: 631/208; 631/326; Agaricales - classification; Agaricales - genetics; Auricularia heimuer; Basidiomycota - genetics; Breeding; EST-SSRs; Expressed Sequence Tags; Gene Expression Profiling - methods; Genetic analysis; Genetic diversity; Genetic Markers; Germplasm; High-Throughput Nucleotide Sequencing; Humanities and Social Sciences; Microsatellite Repeats - genetics; Molecular Sequence Annotation; multidisciplinary; Next-generation sequencing; Phylogeny; Polymorphism, Genetic; Population genetics; Population structure; Science; Science (multidisciplinary); Transcriptome; Transcriptome - genetics; Transcriptomes
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-024-63080-1

Auricularia heimuer , the third most frequently cultivated edible mushroom species worldwide, has high medicinal value. However, a shortage of molecular marker hinders the efficiency and accuracy of genetic breeding efforts for A. heimuer . High-throughput transcriptome sequencing data are essential for gene discovery and molecular markers development. This study aimed to clarify the distribution of SSR loci across the A. heimuer transcriptome and to develop highly informative EST-SSR markers. These tools can be used for phylogenetic analysis, functional gene mining, and molecular marker-assisted breeding of A. heimuer . This study used Illumina high-throughput sequencing technology to obtain A. heimuer transcriptome data. The results revealed 37,538 unigenes in the A. heimuer transcriptome. Of these unigenes, 24,777 (66.01%) were annotated via comparison with the COG, Pfam, and NR databases. Overall, 2510 SSRs were identified from the unigenes, including 6 types of SSRs. The most abundant type of repeats were trinucleotides (1425, 56.77%), followed by mononucleotides (391, 15.58%) and dinucleotides (456, 18.17%). Primer pairs for 102 SSR loci were randomly designed for validity confirmation and polymorphism identification; this process yielded 53 polymorphic EST-SSR markers. Finally, 13 pairs of highly polymorphic EST-SSR primers were used to analyze the genetic diversity and population structure of 52 wild A. heimuer germplasms, revealing that the 52 germplasms could be divided into three categories. These results indicated that SSR loci were abundant in types, numbers, and frequencies, providing a potential basis for germplasm resource identification, genetic diversity analysis, and molecular marker-assisted breeding of A. heimuer .