Search bioRxiv⌕ Search

bioRxiv · 10.1101/336669

Genetic Diversity in Common Carp Stocks from a Natural Reservoir Assayed by Randomly Amplified Polymorphic DNA Markers

Abstract

BackgroundThe common carp (Cyprinus carpio) is a freshwater fish that is cultured throughout the world. C. carpio belongs to the family Cyprinidae, the largest family among freshwater teleosts, accounting for 10 % of total fish production. Specifically, the common carp is cultured in more than 100 countries in worldwide and accounts for over 3 million metric tons of total annual freshwater fish production. The population of common carp (C. carpio) is declining in freshwater reservoirs because of various human activities, such as overfishing, pollution, hybridization with domestic carp, and loss of breeding grounds because of habitat degradation.\n\nResultsIn total, 30 specimens were collected from each of four different locations (WH1, WH2, WH3 and WH4) in the reservoir. Five random decamer primers were used to assay polymorphisms within and between the population of C. carpio. A total of 60 bands were produced by these primers, out of which 50 bands were polymorphic and 10 bands were monomorphic. The mean highest polymorphism (100 %) was observed in the specimen collected from WHS4 stock, followed by 89.05, 87.62 and 76.66 % of the fish collection from WH3, WH2, and WH4, respectively. Neis genetic distance values ranged from 0.0006 to 0.1005. Highest and lowest genetic distance were 0.1005 and 0.006 in fish collected from WH1 and WH2, respectively. Average value of heterozygosity ranged from 0.3008 to 0.3748. A C. carpio UPGMA dendrogram was constructed to observe fish phylogeny. Phylogenetic clusters by RAPD indicated that fish stock of WH2, WH3, and WH4 were closely related to each other.\n\nConclusionIt was concluded that RAPD analysis can be successfully used as a marker to generate information regarding the percent homology within stock of common carp, which may be used to trace the progeny to the parents and is helpful for the improvement of breeding programs.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Mahboob Rana, S., AlGhanim, K., M. A. Al-Mulhim, N. M., No,. 2018-06-01. Genetic Diversity in Common Carp Stocks from a Natural Reservoir Assayed by Randomly Amplified Polymorphic DNA Markers. https://doi.org/10.1101/336669

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Mapping, stacking and characterization of a novel resistance haplotype against GpaVvrn-virulent Globodera pallida derived from wild potato relative Solanum brevicaule

Potato production is threatened by pests and pathogens. Among the most harmful are the potato cyst nematodes (PCN), including Globodera pallida. The major control measures are potato cultivars harbouring resistance genes. However, virulent nematode populations are breaking through the most broadly applied resistance genes, and therefore novel resistance genes are required to keep control of G. pallida. In this study we map a resistance locus in wild potato relative Solanum brevicaule to the bottom of chromosome 11 (42.83 - 42.85 Mb) using a k-mer based bulked segregant analysis and name the resistant haplotype GpaXIbrc. The presence of the GpaXIbrc marker in the potato genome significantly increases resistance against a GpaVvrn-virulent G. pallida population (AMPOP01). Furthermore, the GpaXIbrc haplotype was stacked with three other resistance haplotypes: GpaXItar, GpaVvrn, and GpaIXvrn. Stacking of the novel GpaXIbrc haplotype to these other resistance haplotypes resulted in a significant increase in resistance. The largest effect was seen in combinations with 'major' resistance haplotypes GpaVvrn + GpaIXvrn and GpaXItar + GpaXIbrc. To determine whether we are dealing with a novel allele, the resistance mechanism underlying the GpaXIbrc haplotype was described after performing an in vitro bioassay. The resistance mechanism was different from GpaXIspl as described in literature, which is also localized at the bottom of chromosome 11. Therefore, we conclude that we found a novel resistance allele originating from S. brevicaule.

genetics↗

Cellular context shapes the transcriptomic impact of somatic variants

Somatic SNVs are commonly prioritized by recurrence or sequence annotation, leaving the molecular consequences of private variants unresolved. We developed PrismSNV and Ligo-Seq, a single-cell full-length transcriptome sequencing platform, to quantify transcriptomic displacement associated with within-cell SNV-state toggling. Across 26 samples from three cancer types, more than 60% of candidate SNVs showed significant cell-type-specific displacement with over 30% variation in magnitude. Sequence-based deleteriousness was poorly aligned with cellular displacement, and fewer than 3% of top-displacement SNVs across six tumor types were catalogued in ClinVar. Displacement was strongest in transcriptionally plastic, less differentiated states. Analysis of 655,349 CD4+ T-cell transcriptomes further showed that SNV-gene associations changed in magnitude and sometimes direction during activation. Lack of recurrence or clinical annotation does not imply transcriptomic inertness; variant impact is shaped by cellular context rather than sequence alone, establishing the variant-cell pair as a critical unit for interpreting somatic variation.

genetics↗

Genetic and Epigenetic Landscape of Self-Identified Hispanics/Latino in All Of Us

Human genetic studies still underrepresent many populations, limiting discovery and interpretation of medically relevant variation. Extensive admixture in self-identified Hispanic/Latino populations increases the need for representative reference data and ancestry-aware interpretation of medically relevant variation. We used long-read sequencing to analyze genetic variation, ancestry, and DNA methylation in 1,490 self-identified Hispanic/Latino participants from the All of Us Research Program. We identified 10 million novel variants and more than 100 candidate phenotype associations, with fine-mapping prioritizing structural variants over nearby single-nucleotide variants in more than half. We linked 3,329 tandem repeats to DNA methylation, resolved widespread allele-specific methylation, and identified ancestry-linked regulation across paralogous genes. These results reveal previously inaccessible genetic and regulatory variation and show the value of long-read sequencing for diverse populations.

genetics↗