Comparative analyses of copy number variations between Bos taurus and Bos indicus
Yan Hu1, Han Xia1, Mingxun Li2,3
1Key Laboratory of Agricultural Animal Genetics, Breeding and Reproduction of Ministry of Education & College of Animal Science and Technology, Huazhong Agricultural University, Wuhan, 430070, China.
BMC Genomics
|October 2, 2020
Summary
Copy number variations (CNVs) reveal significant genetic differences between Bos taurus and Bos indicus cattle. These CNVs offer insights into subspecies adaptation and distinct traits, aiding cattle breeding and research.
Area of Science:
- Genomics
- Comparative genomics
- Animal genetics
Background:
- Bos taurus and Bos indicus are the two primary cattle subspecies.
- Differential copy number variations (CNVs) between these subspecies are not well-studied.
Purpose of the Study:
- To identify and compare copy number variation regions (CNVRs) between Bos taurus and Bos indicus.
- To understand the genomic diversity and genetic basis for phenotypic differences.
Main Methods:
- Utilized the ARS-UCD1.2 cattle reference genome.
- Integrated three CNV detection strategies across 73 animals from 10 breeds.
- Analyzed copy number variation regions (CNVRs) and their overlap with genes.
Main Results:
- Identified 13,234 non-redundant CNVRs, with 52.82% shared between subspecies.
- Discovered significant CNV differences enabling subspecies separation.
- Found 2212 and 538 genes uniquely overlapping with indicine-specific and taurine-specific CNVRs, respectively.
- Detected 16 candidate lineage-differential CNV segments under selection, including genes related to heat resistance and metabolism.
Conclusions:
- Presents a genome-wide CNV comparison between Bos taurus and Bos indicus.
- Provides crucial genomic diversity data for understanding adaptation and phenotypic variations.
- Highlights the role of CNVs in differentiating cattle subspecies and their traits.
Related Concept Videos
Comparing Copy Number Variations and SNPs
18.4K
Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
18.4K
Single Nucleotide Polymorphisms-SNPs
17.6K
A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
17.6K
Evolutionary Relationships through Genome Comparisons
6.7K
Genome comparison is one of the excellent ways to interpret the evolutionary relationships between organisms. The basic principle of genome comparison is that if two species share a common feature, it is likely encoded by the DNA sequence conserved between both species. The advent of genome sequencing technologies in the late 20th century enabled scientists to understand the concept of conservation of domains between species and helped them to deduce evolutionary relationships across diverse...
6.7K
Pedigree Analysis
88.2K
Overview
88.2K
Incomplete Dominance
29.2K
Gregor Mendel's work (1822 - 1884) was primarily focused on pea plants. Through his initial experiments, he determined that every gene in a diploid cell has two variants called alleles inherited from each parent. He suggested that amongst these two alleles, one allele is dominant in character and the other recessive. The combination of alleles determines the phenotype of a gene in an organism.
29.2K
Multiple Comparison Tests
4.3K
Multiple comparison test, abbreviated as MCT, is a post hoc analysis generally performed after comparing multiple samples with one or more tests. An MCT will help identify a significantly different sample among multiple samples or a factor among multiple factors.
It would be easy to compare two samples using a significance alpha level of 0.05. In other words, there is only one sample pair to be compared. However, it would be difficult to identify a significantly different sample if the number...
It would be easy to compare two samples using a significance alpha level of 0.05. In other words, there is only one sample pair to be compared. However, it would be difficult to identify a significantly different sample if the number...
4.3K


