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用于蓝莓遗传应用的新型转录组衍生SSR标记的开发与表征

Generation and characterization of novel transcriptome-derived SSR markers for genetic applications in blueberry.

作者信息

Kulkarni Krishnanand P, Appiah Richmond K, Johnson-Cicalese Jennifer, Vorsa Nicholi, Reddy Umesh K, Elavarthi Sathya, Bostan Hamed, Iorizzo Massimo, Melmaiee Kalpalatha

机构信息

Department of Agriculture and Natural Resources, Delaware State University, Dover, DE, 19901, USA.

Department of Plant Biology, Rutgers University, New Brunswick, NJ, 08901, USA.

出版信息

Sci Rep. 2025 Jul 11;15(1):25050. doi: 10.1038/s41598-025-10317-2.

Abstract

Blueberries (Vaccinium spp.) are small fruit crops native to North America but grown commercially in several countries. There has been a steady increase in consumer demand for blueberries, owing to their numerous health benefits attributable to the high content of antioxidant compounds. Despite its importance, limited genomic resources are available, hindering genetic research and improvement in blueberry. In this study, we developed novel transcriptome-derived simple sequence repeat (SSR) markers from two divergent blueberry species. We identified 64,013 SSRs from 208,286 unigenes de novo assembled from 135 million high-quality sequence reads. SSRs with mononucleotide repeat motifs were most abundant, followed by di-, tri-, tetra-, penta-, and hexanucleotide repeat motifs. The repeat motif AG/CT was most abundant (84%) compared to the other three dinucleotide repeat motifs, AC/TG, AT/TA, and CG/GC. Similarly, AAG/CTT and AAAT/ATTT were the most abundant tri- and tetra-nucleotide repeat motifs, respectively. We designed 33,179 primer pairs from 64,013 SSR motifs. Genomic coordinates of these primers were identified using a chromosome-scale reference genome sequence of diploid blueberry clone W85-20. After discarding those markers mapped with MapQ < 1, genomic positions for 19,310 markers were identified. Thirty-six SSRs differing in nucleotide repeat motifs were randomly selected for PCR optimization, characterization, and amplification in 45 diverse Vaccinium species. Thirty-four primers generated 158 alleles with an average of 4.6 alleles per locus. Genetic structure analyses revealed a high genetic differentiation among the selected species, and divided 45 accessions into two to five clusters. Furthermore, the selected SSR markers showed 88.2-97% cross-species transferability, suggesting the possibility of using these markers for various genetics and comparative genomics applications in blueberry and cranberry species. Thus, the transcriptome-derived SSR markers developed in this study could serve as a valuable resource for further genetic and evolutionary studies in Vaccinium species.

摘要

蓝莓(越橘属)是原产于北美的小型水果作物,但在多个国家进行商业化种植。由于其富含抗氧化化合物而具有诸多健康益处,消费者对蓝莓的需求一直在稳步增长。尽管蓝莓很重要,但其基因组资源有限,这阻碍了蓝莓的遗传研究和改良。在本研究中,我们从两个不同的蓝莓物种中开发了新型转录组衍生简单序列重复(SSR)标记。我们从1.35亿条高质量序列读数中从头组装的208,286个单基因中鉴定出64,013个SSR。单核苷酸重复基序的SSR最为丰富,其次是二、三、四、五和六核苷酸重复基序。与其他三个二核苷酸重复基序AC/TG、AT/TA和CG/GC相比,重复基序AG/CT最为丰富(84%)。同样,AAG/CTT和AAAT/ATTT分别是最丰富的三核苷酸和四核苷酸重复基序。我们从64,013个SSR基序中设计了33,179对引物。使用二倍体蓝莓克隆W85-20的染色体规模参考基因组序列确定了这些引物的基因组坐标。在舍弃那些MapQ < 1映射的标记后,确定了19,310个标记的基因组位置。随机选择36个核苷酸重复基序不同的SSR进行PCR优化、表征,并在45个不同的越橘属物种中进行扩增。34对引物产生了158个等位基因,每个位点平均有4.6个等位基因。遗传结构分析揭示了所选物种之间的高度遗传分化,并将45个种质分为两到五个簇。此外,所选的SSR标记显示出88.2 - 97%的跨物种转移性,这表明有可能将这些标记用于蓝莓和蔓越莓物种的各种遗传学和比较基因组学应用。因此,本研究中开发的转录组衍生SSR标记可作为越橘属物种进一步遗传和进化研究的宝贵资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/059b/12254408/ec1a37ad6c47/41598_2025_10317_Fig1_HTML.jpg

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