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Functional CENP-B boxes are selectively conserved at centromeric regions

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Abstract Human centromeres are built over large stretches of repetitive, divergent α-satellite DNA. Within these sequences lies a conserved, defined 17-bp sequence named the CENP-B box that is bound by the DNA-binding protein CENP-B. Recent studies have proposed that CENP-B box motifs along chromosome arms exist and may represent conserved, ectopic binding sites with functional relevance. Here, we evaluate the genomic distribution, conservation, and binding capacity of different CENP-B box motifs outside canonical centromeres. Analysis of thousands of complete human centromere assemblies reveals exceptional conservation of a unique and canonical CENP-B box motif within centromeres. This is in contrast with the high sequence variability and stochastic occurrence of more degenerate CENP-B box motifs along chromosome arms. Consistently, CENP-B binds only at canonical CENP-B box motifs embedded within α-satellite sites, with no evidence of functional binding at any ectopic sites. Together, these results indicate an adaptive selection of canonical CENP-B boxes within centromeric regions, in contrast to random sequence occurrences for ectopic CENP-B box-like motifs.
Title: Functional CENP-B boxes are selectively conserved at centromeric regions
Description:
Abstract Human centromeres are built over large stretches of repetitive, divergent α-satellite DNA.
Within these sequences lies a conserved, defined 17-bp sequence named the CENP-B box that is bound by the DNA-binding protein CENP-B.
Recent studies have proposed that CENP-B box motifs along chromosome arms exist and may represent conserved, ectopic binding sites with functional relevance.
Here, we evaluate the genomic distribution, conservation, and binding capacity of different CENP-B box motifs outside canonical centromeres.
Analysis of thousands of complete human centromere assemblies reveals exceptional conservation of a unique and canonical CENP-B box motif within centromeres.
This is in contrast with the high sequence variability and stochastic occurrence of more degenerate CENP-B box motifs along chromosome arms.
Consistently, CENP-B binds only at canonical CENP-B box motifs embedded within α-satellite sites, with no evidence of functional binding at any ectopic sites.
Together, these results indicate an adaptive selection of canonical CENP-B boxes within centromeric regions, in contrast to random sequence occurrences for ectopic CENP-B box-like motifs.

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