Ravishankar K V, Vasudeva R, Hemanth Byatroy, Sandya B S, Sthapit B R, Parthasarathy V A, Rao V Ramanatha
ICAR-Indian Institute of Horticultural Research, Bengaluru 560 089, India.
J Genet. 2017 Jun;96(2):213-218. doi: 10.1007/s12041-017-0756-0.
Garcinia gummi-gutta (L.) Roxb. (Clusiaceae) is an endemic, semidomesticated, fruit-yielding tree species distributed in the Western Ghats of India and Sri Lanka. Various bioactive phytochemicals, such as garcinol, benzophenones and xanthones are isolated from G. gummi-gutta and have shown antibacterial, antiviral and antioxidant activities. We sequenced the total genomic DNA using Illumina Hiseq 2000 platform and examined 241,141,804 bp high quality data, assembled into 773,889 contigs. In these contigs, 27,313 simple-sequence repeats (SSRs) were identified, among which mononucleotide repeats were predominant (44.98%) followed by dinucleotide and trinucleotide repeats. Primers were designed for 9964 microsatellites among which 32 randomly selected SSR primer pairs were standardized for amplification. Polymerase chain reaction (PCR) amplification of genomic DNA in 30 G. gummi-gutta genotypes revealed polymorphic information content (PIC) across all 32 loci ranging from 0.867 to 0.951, with a mean value of 0.917. The observed and expected heterozygosity ranged from 0.00 to 0.63 and 0.896 to 0.974, respectively. Alleles per locus ranged from 12 to 27. This is the first report on the development of genomic SSR markers in G. gummi-gutta using next-generation sequencing technology. The genomic SSR markers developed in this study will be useful in identification, mapping, diversity and breeding studies.
藤黄(Garcinia gummi - gutta (L.) Roxb.,藤黄科)是一种特产于印度西高止山脉和斯里兰卡的半驯化结果树。从藤黄中分离出了多种生物活性植物化学物质,如藤黄醇、二苯甲酮和呫吨酮,它们具有抗菌、抗病毒和抗氧化活性。我们使用Illumina Hiseq 2000平台对总基因组DNA进行了测序,并检查了241,141,804 bp的高质量数据,这些数据组装成了773,889个重叠群。在这些重叠群中,鉴定出了27,313个简单序列重复序列(SSR),其中单核苷酸重复序列占主导(44.98%),其次是二核苷酸和三核苷酸重复序列。为9964个微卫星设计了引物,其中随机选择了32对SSR引物对进行扩增标准化。对30个藤黄基因型的基因组DNA进行聚合酶链反应(PCR)扩增,结果显示所有32个位点的多态信息含量(PIC)在0.867至0.951之间,平均值为0.917。观察到的杂合度和预期杂合度分别在0.00至0.63和0.896至0.974之间。每个位点的等位基因数在12至27之间。这是关于利用下一代测序技术开发藤黄基因组SSR标记的首次报道。本研究中开发的基因组SSR标记将有助于鉴定、图谱绘制、多样性和育种研究。