» Articles » PMID: 25071822

Identification of Structural Variation in Mouse Genomes

Overview
Journal Front Genet
Date 2014 Jul 30
PMID 25071822
Citations 14
Authors
Affiliations
Soon will be listed here.
Abstract

Structural variation is variation in structure of DNA regions affecting DNA sequence length and/or orientation. It generally includes deletions, insertions, copy-number gains, inversions, and transposable elements. Traditionally, the identification of structural variation in genomes has been challenging. However, with the recent advances in high-throughput DNA sequencing and paired-end mapping (PEM) methods, the ability to identify structural variation and their respective association to human diseases has improved considerably. In this review, we describe our current knowledge of structural variation in the mouse, one of the prime model systems for studying human diseases and mammalian biology. We further present the evolutionary implications of structural variation on transposable elements. We conclude with future directions on the study of structural variation in mouse genomes that will increase our understanding of molecular architecture and functional consequences of structural variation.

Citing Articles

The Genomic Landscape, Causes, and Consequences of Extensive Phylogenomic Discordance in Murine Rodents.

Thomas G, Hughes J, Kumon T, Berv J, Nordgren C, Lampson M Genome Biol Evol. 2025; 17(2).

PMID: 39903560 PMC: 11837218. DOI: 10.1093/gbe/evaf017.


Structural variations in livestock genomes and their associations with phenotypic traits: a review.

Chen Y, Khan M, Wang X, Liang H, Ren W, Kou X Front Vet Sci. 2024; 11:1416220.

PMID: 39600883 PMC: 11588642. DOI: 10.3389/fvets.2024.1416220.


The role of copy-number variation in the reinforcement of sexual isolation between the two European subspecies of the house mouse.

North H, Caminade P, Severac D, Belkhir K, Smadja C Philos Trans R Soc Lond B Biol Sci. 2020; 375(1806):20190540.

PMID: 32654648 PMC: 7423270. DOI: 10.1098/rstb.2019.0540.


De novo genome assembly of the cichlid fish Astatotilapia latifasciata reveals a higher level of genomic polymorphism and genes related to B chromosomes.

Jehangir M, Ahmad S, Cardoso A, Ramos E, Valente G, Martins C Chromosoma. 2019; 128(2):81-96.

PMID: 31115663 DOI: 10.1007/s00412-019-00707-7.


Characterization of hepatitis B virus with complex structural variations.

Fujiwara K, Matsuura K, Matsunami K, Iio E, Nojiri S BMC Microbiol. 2018; 18(1):202.

PMID: 30509169 PMC: 6276219. DOI: 10.1186/s12866-018-1350-1.


References
1.
Nelson T, Munger S, Boughter Jr J . Haplotypes at the Tas2r locus on distal chromosome 6 vary with quinine taste sensitivity in inbred mice. BMC Genet. 2005; 6:32. PMC: 1181811. DOI: 10.1186/1471-2156-6-32. View

2.
Lee S, Hormozdiari F, Alkan C, Brudno M . MoDIL: detecting small indels from clone-end sequencing with mixtures of distributions. Nat Methods. 2009; 6(7):473-4. DOI: 10.1038/nmeth.f.256. View

3.
Rausch T, Zichner T, Schlattl A, Stutz A, Benes V, Korbel J . DELLY: structural variant discovery by integrated paired-end and split-read analysis. Bioinformatics. 2012; 28(18):i333-i339. PMC: 3436805. DOI: 10.1093/bioinformatics/bts378. View

4.
Li J, Akagi K, Hu Y, Trivett A, Hlynialuk C, Swing D . Mouse endogenous retroviruses can trigger premature transcriptional termination at a distance. Genome Res. 2012; 22(5):870-84. PMC: 3337433. DOI: 10.1101/gr.130740.111. View

5.
Manske H, Kwiatkowski D . LookSeq: a browser-based viewer for deep sequencing data. Genome Res. 2009; 19(11):2125-32. PMC: 2775587. DOI: 10.1101/gr.093443.109. View