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  1. Intercalary heterochromatin and genetic silencing.Igor F. Zhimulev & Elena S. Belyaeva - 2003 - Bioessays 25 (11):1040-1051.
    We focus here on the intercalary heterochromatin (IH) of Drosophila melanogaster and, in particular, its molecular properties. In the polytene chromosomes of Drosophila, IH is represented by a reproducible set of dense bands scattered along the euchromatic arms. IH contains mainly unique DNA sequences, and shares certain features with other heterochromatin types such as pericentric, telomeric, and PEV‐induced heterochromatin, the inactive mammalian X‐chromosome and the heterochromatized male chromosome set in coccids. These features are transcriptional silencing, chromatin compactness, late DNA replication, (...)
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  • The vagaries of variegating transgenes.David I. K. Martin & Emma Whitelaw - 1996 - Bioessays 18 (11):919-923.
    Expression of transgenes in mice, when examined with assays that can distinguish individual cells, is often found to be heterocellular, or variegated. Line‐to‐line variations in expression of a transgene may be due largely to differences in the proportion of cells in which it is expressed. Variegated silencing by centromeric heterochromatin is well described, but other factors may also affect transgene silencing in mice. Tandem arrays of transgenes themselves form heterochromatin, and some cell lineages may tend to silence transgenes because of (...)
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  • Chromosomal elements conferring epigenetic inheritance.Frank Lyko & Renato Paro - 1999 - Bioessays 21 (10):824-832.
  • Dosage‐dependent modification of position‐effect variegation in Drosophla.Steven Henikoff - 1996 - Bioessays 18 (5):401-409.
    Many loci in Drosophila exhibit dosage effects on single phenotypes. In the case of modifiers of position‐effect variegation, increases and decreases in dosage can have opposite effects on variegating phenotypes. This is seemingly paradoxical: if each locus encodes a limiting gene product sensitive to dosage decreases, then increasing the dosage of any one should have no effect, because the others should remain limiting. An earlier model put forward to resolve this paradox suggested that dosage‐dependent modifiers encode protein subunits of a (...)
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  • How Communication Between Nucleosomes Enables Spreading and Epigenetic Memory of Histone Modifications.Fabian Erdel - 2017 - Bioessays 39 (12):1700053.
    Nucleosomes “talk” to each other about their modification state to form extended domains of modified histones independently of the underlying DNA sequence. At the same time, DNA elements promote modification of nucleosomes in their vicinity. How do these site-specific and histone-based activities act together to regulate spreading of histone modifications along the genome? How do they enable epigenetic memory to preserve cell identity? Many models for the dynamics of repressive histone modifications emphasize the role of strong positive feedback loops, which (...)
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  • Transcriptional silencing of homeotic genes in drosophila.Mariann Bienz & Jürg Müller - 1995 - Bioessays 17 (9):775-784.
    Homeotic genes are subject to transcriptional silencing, which prevents their expression in inappropriate body regions. Here, we shall focus on Drosophila, as little is known about this process in other organisms. Evidence is accumulating that silencing of Drosophila homeotic genes is conferred by two types of cis‐regulatory sequences: initiation (SIL‐I) and maintenance (SIL‐M) elements. The former contain target sites for transient repressors with a highly localised distribution in the early embryo and the latter for constitutive repressors that are likely to (...)
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