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Telomere-to-telomere human DNA replication timing profiles

Dashiell J. Massey, Amnon Koren

Preprint posted on March 29, 2022 https://www.biorxiv.org/content/10.1101/2022.03.28.486072v1

Article now published in Scientific Reports at http://dx.doi.org/10.1038/s41598-022-13638-8

Filling gaps in centromeric replication timing

Selected by Jennifer Ann Black

Categories: genomics

Background:

In most eukaryotes, DNA replication completes during S phase, but not all regions are copied at the same time. Much work across several eukaryotes has shown that cells have a defined program (or pattern) of DNA replication, which is very stable, conserved (in some cases) and hard to interfere with. Why genome duplication is organised into such a defined program is unknown, but it may help cells regulate gene expression and/or diversify (1). Until recently, ~8% of the human genome was missing from the reference, including the centromeres, which are the sites of spindle fibre attachment for chromosome segregation. They were hard to assemble due to being very repetitive. This meant our understanding of replication dynamics at centromeres was limited due to their less robust assembly, yet alterations to the centromere environment and re-replication of centromeres associates with aneuploidy (abnormal chromosome numbers). Improving our understanding of centromere replication may provide insights into aneuploidy driven genetic diseases (2,3,4). Recently, the Telomere-to-Telomere (T2) Consortium published a new and largely gapless genome assembled from long-read sequences and refined by short-read and long-read sequence data (5). This new assembly now opening the ability to study RT across almost every site in the genome.

Key Findings:

Previously, the authors analysed the RT program across 5 different cell lines (including from healthy and cancerous cells). They performed these experiments by comparing the sequencing depth of the DNA from replicating (S-phase) cells with non-replicating (G1) cells, which were isolated using flow cytometry. By mapping the sequence reads onto a reference genome and looking for regions of increased coverage in S-phase cells relative to G1- cells, the RT can be studied. Replicating regions (initiation sites) have a ‘peak’ like appearance when plotted and regions of reduced coverage (i.e non-replicating) appear as valleys (6). They previously revealed centromeric sites replicate mid-late S-phase and show discrete patterns of replication timing (RT) within cells and between the different cell types. Here, the authors re-map their previous datasets to the new genome to better understand how the centromeres replicate.


Figure shows a schematic representation of a human centromere adapted from Aldrup-Macdonald and Sullivan, 2014. The Past, Present and Future of Human Centromere Genomics. Lower plots show replication timing compared between centromeric (green) and non-centromeric (grey) regions for each type of repeat. Figure adapted from Massey and Koren, 2022, https://www.biorxiv.org/content/10.1101/2022.03.28.486072v1.

1) Repetitive sequence elements associated with centromeric sites have distinct RT programs

Centromeres in humans are made of arrays of repeat-rich families (satellite sequence elements), the most abundant of which are the alpha-satellite arrays. These arrays are then organised into Higher Order Repeats (HORs) which are considered as a basic repeat unit. HORs are neighboured by other repeat families. Here, the authors show that different satellite families within centromeres appear to have different replication timings, for example alpha-satellite HORs were generally replicated earlier compared to other repeats. Why this happens is unclear, but the authors suggest this staggered timing could help to make sure the centromere is prepared for division i.e the kinetochore structure (for spindles to attach) is assembled.

 

2) Centromeres replicate mid-late S-phase, and their RT varies from cell-to-cell

Like their prior study, the authors show that centromeric regions replication mid-late S-phase and that RT within centromeres was shown to vary from cell line to cell line. In some cell lines the centromeres, on average, replicated earlier during mid-late S-phase, and in others, late. In this new analysis, the authors could examine these RT dynamics in more detail at individual centromeres. They found cell lines with earlier (or later) replicating centromeres always had earlier (or later) replicating centromeres. This suggests that overall centromere structure is replicated at the same time during DNA replication in the same cell line, irrespective of how big or small each chromosome is, or the repeat sequences associated with the centromeres in each cell line. Why centromeric timing is largely similar is also unclear but could suggests a biological pathway works to keep centromeric duplication largely the same across each chromosome; perhaps by physical interactions within the chromosomes themselves or by the positioning in the nucleus (7,8).

 

What I liked about this preprint:

I liked the fact that in this preprint, the authors went back to datasets they already produced and re-analysed their data with the mind to refine and improve the analysis as new information became available in the field. They largely confirm their previous analyses whilst additionally uncovering additional information on centromeric RT. It will be curious to understand further what process/processes govern the timing of centromeric duplication and why it differs between cell lines.

 

Questions for the authors:

Q1: Your data suggests that repeat region timing could be staggered within a centromere. What do you think might be the underlying mechanism? Is there evidence of alternative epigenetic marks associated with different repeats regions or?

Q2: Centromeric replication also appears to require DNA repair activities. Do you think that staggering replication of highly repetitive sequences (which are often prone to instability) may relate to DNA repair activities required, and if so, how? Are the later replicated repeat region more prone to instability for example?

Q3: What could be the advantage of largely maintaining a similar centromere replication timing across all chromosomes within a cell line? Do you think this could explain some aspects of a diseased cell state i.e alteration of one centromeric RT timing affects the timing of the others leading instability?

References:

  1. Marchal, J. Sima and D.M. Gilbert. Control of DNA replication timing in the 3D genome. Nat. Rev. Mol. Cell. Bio. 2019.
  2. Barra and D. Fachinetti. The dark side of centromeres: types, causes and consequences of structural abnormalities implicating centromeric DNA. Nat. Comms. 2018.
  3. Giunta et al. CENP-A chromatin prevents replication stress at centromeres to avoid structural aneuploidy. PNAS. 2021.
  4. L. Hanlon and J.J. Li. Re-replication of a centromere induces chromosomal instability and aneuploidy. PLoS Genetics. 2015.
  5. Nurk et al. The complete sequence of a human genome. Science. 2022.
  6. J. Massey, D. Kim, K.E. Brooks, M.B. Smolka and A. Koren. Next-Generation sequencing enables spatiotemporal resolution of human centromere replication timing. Genes. 2019.
  7. Duan et al. A three-dimensional model of the yeast genome. Nature. 2010.
  8. E Wiblin, W. Cui, A.J. Clark and W.A. Bickmore. Distinctive nuclear organisation of centromeres and regions involved in pluripotency in human embryonic stem cells. J. Cell. Sci. 2005.

Tags: centromere, repeats, replication, t2t

Posted on: 4th May 2022

doi: https://doi.org/10.1242/prelights.31917

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