Development of Genetic Markers for Sex and Individual Identification of the Japanese Giant Flying Squirrel (Petaurista leucogenys) by an Efficient Method Using High-throughput DNA Sequencing

被引:0
作者
Sugita, Aki [1 ]
Shigeta, Mayumi [2 ]
Tamura, Noriko [2 ]
Okazaki, Hiroyuki [3 ]
Kutsukake, Nobuyuki [1 ,4 ]
Terai, Yohey [1 ,4 ]
机构
[1] SOKENDAI Grad Univ Adv Studies, Dept Evolutionary Studies Biosyst, Hayama, Kanagawa 2400193, Japan
[2] Forestry & Forest Prod Res Inst, Tama Forest Sci Garden, 1833-81 Todori, Hachioji, Tokyo 1930843, Japan
[3] Chuo Univ, Jr & Senior High Sch, 3-22-1 Nukuikita Town, Koganei, Tokyo 1848575, Japan
[4] SOKENDAI Grad Univ Adv Studies, Res Ctr Integrat Evolutionary Sci, Hayama, Kanagawa 2400193, Japan
关键词
sex identification; individual identification; microsatellite marker; fecal DNA; non-invasive sampling; Japanese giant flying squirrel; MICROSATELLITE MARKERS; DETERMINING REGION; RED SQUIRREL; SCIURUS-VULGARIS; BLACK; AMPLIFICATION; SIZE; CHROMOSOME; DIET; DIMORPHISM;
D O I
10.2108/zs220045
中图分类号
Q95 [动物学];
学科分类号
071002 ;
摘要
DNA markers that detect differences in the number of microsatellite repeats can be highly effective for genotyping individuals that lack differences in external morphology. However, isolation of sequences with different microsatellite repeat numbers between individuals has been a time-consuming process in the development of DNA markers. Individual identification of Japanese giant flying squirrels (Petaurista leucogenys) has been challenging because this species is arboreal and nocturnal and exhibits little to no morphological variation between individuals. In this study, we developed DNA markers for sex and individual identification of this species by an efficient method using high-throughput DNA sequence data. Paired- end 5 Gb (2 x 250 bp) and 15 Gb (2 x 150 bp) genome sequences were determined from a female and a male Japanese giant flying squirrel, respectively. We searched SRY and XIST genes located on Y and X chromosomes, respectively, from high-throughput sequence data and designed primers to amplify these genes. Using these primer sets, we succeeded to identify the sex of individuals. In addition, we selected 12 loci containing microsatellites with different numbers of repeats between two individuals from the same data set, and designed primers to amplify these sequences. Twenty individuals from nine different locations were discriminated using these primer sets. Furthermore, both sex and microsatellite markers were amplified from DNA extracted non-invasively from single fecal pellet samples. Based on our results for flying squirrels, we expect our efficient method for developing non-invasive high-resolution individual- and sex-specific genotyping to be applicable to a diversity of mammalian species.
引用
收藏
页码:24 / 31
页数:8
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