English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Modelling segmental duplications in the human genome

MPS-Authors
/persons/resource/persons228516

Abdullaev,  Eldar
Evolutionary Genomics (Peter Arndt), Dept. of Computational Molecular Biology (Head: Martin Vingron), Max Planck Institute for Molecular Genetics, Max Planck Society;

/persons/resource/persons50074

Arndt,  Peter F.
Evolutionary Genomics (Peter Arndt), Dept. of Computational Molecular Biology (Head: Martin Vingron), Max Planck Institute for Molecular Genetics, Max Planck Society;

External Resource
No external resources are shared
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)

Abdullaev_2021.pdf
(Publisher version), 2MB

Supplementary Material (public)
There is no public supplementary material available
Citation

Abdullaev, E., Umarova, I. R., & Arndt, P. F. (2021). Modelling segmental duplications in the human genome. BMC Genomics, 22: 496. doi:10.1186/s12864-021-07789-7.


Cite as: https://hdl.handle.net/21.11116/0000-0009-0FD5-7
Abstract
Background: Segmental duplications (SDs) are long DNA sequences that are repeated in a genome and have high
sequence identity. In contrast to repetitive elements they are often unique and only sometimes have multiple copies in
a genome. There are several well-studied mechanisms responsible for segmental duplications: non-allelic homologous
recombination, non-homologous end joining and replication slippage. Such duplications play an important role in
evolution, however, we do not have a full understanding of the dynamic properties of the duplication process.
Results: We study segmental duplications through a graph representation where nodes represent genomic regions
and edges represent duplications between them. The resulting network (the SD network) is quite complex and has
distinct features which allow us to make inference on the evolution of segmantal duplications. We come up with the
network growth model that explains features of the SD network thus giving us insights on dynamics of segmental
duplications in the human genome. Based on our analysis of genomes of other species the network growth model
seems to be applicable for multiple mammalian genomes.
Conclusions: Our analysis suggests that duplication rates of genomic loci grow linearly with the number of copies of
a duplicated region. Several scenarios explaining such a preferential duplication rates were suggested.