Figure 1.
(A) In Drosophila male GSCs, old (H3–H4)2 are preferentially recycled to the leading strand with yet-to-be identified mechanisms [12]. By default, newly synthesized (H3–H4)2 are incorporated by the lagging strand, thereby generating a biased histone incorporation in a strand biased manner. (B) In mESCs, the role of Mcm2 is shown to recycle old (H3–H4)2 towards the lagging strand [66]. (C) In yeast, old histones recycle towards leading strand via interactions with Dpb3/Dpb4-Polε [68], while the MCM2-ctf4-Polα axis is shown to recycle old (H3–H4)2 towards the lagging strand [67].
Models for replication-coupled nucleosome assembly (RCNA) highlighting old histone H3–H4 recycling.

(A) In Drosophila male GSCs, old (H3–H4)2 are preferentially recycled to the leading strand with yet-to-be identified mechanisms [12]. By default, newly synthesized (H3–H4)2 are incorporated by the lagging strand, thereby generating a biased histone incorporation in a strand biased manner. (B) In mESCs, the role of Mcm2 is shown to recycle old (H3–H4)2 towards the lagging strand [66]. (C) In yeast, old histones recycle towards leading strand via interactions with Dpb3/Dpb4-Polε [68], while the MCM2-ctf4-Polα axis is shown to recycle old (H3–H4)2 towards the lagging strand [67].

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