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Multiple histone chaperones have been implicated in the H3-K56 acycleation cycle, most notably Asf1p which binds one histone H3/H4 dimer and is absolutely required for H3-K56 acetylation by Rtt109p [48] [50] which in turn favors histone H3 binding to the Rtt106p and CAF1 histone chaperones [26].
However, in contrast to yeast, plants possess multiple histone chaperones in most of the families and mutant analyses have shown that cellular function of the members of some of the families is redundant [ 19, 35, 41].
Meanwhile, multiple histone chaperones, modification enzymes, and numerous chromatin remodelers are recruited to ensure the precise duplication of both the genome and the epigenome (Alabert and Groth, 2012; Whitehouse and Smith, 2013).
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Multiple studies showed that the depletion of the histone chaperones Asf1 and CAF-1 results in a slow down of DNA synthesis during S phase (Hoek and Stillman, 2003; Ye et al., 2003; Nabatiyan and Krude, 2004; Groth et al., 2007; Takami et al., 2007) preceding the accumulation of DNA damage in mammalian cells (Hoek and Stillman, 2003; Ye et al., 2003).
Multiple sequence alignment of proteins belonging to ASF1/CIA family of histone chaperones from diverse eukaryotes.
Most of the genes encoding histone chaperones showed differential expression in response to multiple abiotic stresses.
Multiple sequence alignment of proteins belonging to NASP family of histone chaperones from diverse eukaryotes.
Multiple sequence alignment of proteins belonging to NAP family of histone chaperones from diverse eukaryotes.
Multiple sequence alignment of proteins belonging to HIRA family of histone chaperones from diverse eukaryotes.
Multiple sequence alignment of proteins belonging to CAF1A sub-family of histone chaperones from diverse eukaryotes.
Multiple sequence alignment of proteins belonging to SSRP sub-family of histone chaperones from diverse eukaryotes.
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