Kim Sohee, Lee Hwayong
Department of Forest Science, Chungbuk National University, Cheongju, Republic of Korea.
Mycobiology. 2025 Jan 22;53(1):57-71. doi: 10.1080/12298093.2024.2444013. eCollection 2025.
In this study, we aimed to develop simple sequence repeat (SSR) markers for evaluating resources in and examine their transferability to related species. SSR markers were developed using the released whole-genome sequence (GenBank assembly accession: GCA_900157425.1). The SSR regions were analyzed using the MISA (MIcroSAtellite identification tool) program. A total of 2319 SSR loci consisting of 922 (39.76%) mononucleotide, 763 (32.90%) trinucleotide, and 517 (22.29%) dinucleotide motifs were identified. Marker design involved an arbitrary choice of 150 SSR loci, considering motif abundance. A total of 22 strains of were analyzed using the developed markers, and 105 markers were successfully amplified. The mean values of major allele frequency, number of alleles, expected heterozygosity, observed heterozygosity, and polymorphism information content (PIC) values were approximately 5.89, 5.4, 0.541, 0.255, and 0.504, respectively. was analyzed, and 52 markers (49.5%) were successfully amplified to evaluate the transferability of the developed SSR markers. When these markers were used, the mean values of major allele frequency, number of alleles, expected heterozygosity, observed heterozygosity, and PIC were calculated to be approximately 0.615, 4.3, 0.517, 0.133, and 0.502, respectively. In conclusion, SSR markers were developed using the genome of , and some of these markers exhibited transferability to . These results can be used for resource evaluation of and .
在本研究中,我们旨在开发简单序列重复(SSR)标记以评估[物种名称1]的资源,并检验其在[物种名称2]相关物种中的可转移性。利用已发布的[物种名称1]全基因组序列(GenBank组装登录号:GCA_900157425.1)开发SSR标记。使用MISA(微卫星识别工具)程序分析SSR区域。共鉴定出2319个SSR位点,其中包括922个(39.76%)单核苷酸基序、763个(32.90%)三核苷酸基序和517个(22.29%)二核苷酸基序。考虑到基序丰度,标记设计涉及任意选择150个SSR位点。使用开发的标记对总共22株[物种名称1]进行分析,成功扩增出105个标记。主要等位基因频率、等位基因数量、期望杂合度、观察杂合度和多态性信息含量(PIC)值的平均值分别约为5.89、5.4、0.541、0.255和0.504。对[物种名称2]进行分析,成功扩增出52个标记(49.5%)以评估所开发SSR标记的可转移性。当使用这些标记时,主要等位基因频率、等位基因数量、期望杂合度、观察杂合度和PIC的平均值经计算分别约为0.615、4.3、0.517、0.133和0.502。总之,利用[物种名称1]的基因组开发了SSR标记,其中一些标记在[物种名称2]中表现出可转移性。这些结果可用于[物种名称1]和[物种名称2]的资源评估。