Abstract

Author SummaryVariations in the copy number of DNA segments account for a substantial amount of genome diversity of most organisms. DNA amplification, a contributor to copy number variation, can occur in response to various stresses or after altered growth conditions, leading to extensive and often reversible genetic variation. DNA amplification in the parasite Leishmania occurs outside the normal chromosomes and arises by DNA rearrangements involving homologous repeated sequences. We show here that such repeated sequences are widespread in the Leishmania genome and that most of the Leishmania genome is subject to stochastic gene rearrangements mediated by these low-copy repeat sequences. Thus, although cells in the population have a common core genome, many individual cells will differ from the rest of the population by carrying one or more distinct extrachromosomal amplicon. Upon selection with either drugs or culture conditions, a subpopulation can emerge where the amplicon copy number per cell increases, and this clone of cells can then expand to dominate the population. We propose that Leishmania uses adaptive gene amplification at a genome-wide scale as one strategy to adapt to a changing environment.

Highlights

  • Copy number variations (CNVs) account for a substantial amount of genomic variability in mammalian genomes

  • Genome-Wide Distribution of Repeated Sequences in Leishmania The noncoding direct repeated sequences (DRs) used for DHFR-TS amplification are highly conserved (86% identical) between Leishmania major and Leishmania infantum [28]

  • This interspecies conservation led us to hypothesize that either specific loci are subjected to considerable CNVs or alternatively that the Leishmania genome has more repeated sequences than initially anticipated

Read more

Summary

Introduction

Copy number variations (CNVs) account for a substantial amount of genomic variability in mammalian genomes (reviewed in [1]). DNA amplification, a contributor of CNVs, has been reported in response to various stresses or after altered growth conditions, and can lead to extensive and often reversible genetic variations (reviewed in [2,3]). Several models have been proposed to explain DNA amplification mechanisms [2,3,4]. Extrachromosomal circular DNAs can be the products of gene amplification in mammalian cells and in the protozoan parasite Leishmania (reviewed in [5,6]). In Leishmania, DNA circles are generated by homologous recombination (HR) between direct repeated sequences (DRs) (Figure 1A) [7,8]. DNA amplification can lead to palindrome formation. Increasing evidence suggests that palindromes are initiated at the level of inverted repeats (IRs)

Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call