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Volume 271,
Number 10,
Issue of March 8, 1996 pp. 5819-5823
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
A
Naturally Occurring T A Tract Blocks
Nucleosome Formation Over the Human Neurofibromatosis Type 1 (NF1)-Alu
Element
(Received for publication, October 24,
1995; and in revised form, December 28, 1995)
Ella W.
Englander,
Bruce
H.
Howard
The nature of chromatin organization over Alu repetitive
elements is of interest with respect to the maintenance of their
transcriptional silencing as well as their potential to influence local
chromatin structure. We previously demonstrated that the pattern of
nucleosomal organization over Alu elements in native chromatin is
specific and similar to the pattern observed with an in vitro reconstituted Alu template. This pattern, distinguished by a
nucleosome centered over the 5`-end of the Alu element, is associated
with repression of polymerase III-dependent transcription in vitro (Englander, E. W., Wolffe, A. P., and Howard, B. H.(1993) J.
Biol. Chem. 268, 19565-19573; Englander, E. W., and Howard,
B. H.(1995) J. Biol. Chem. 270, 10091-10096). In the
current study, additional templates representing both evolutionarily
old and young Alu subfamilies were found to direct a similar pattern of
nucleosome assembly, consistent with the view that nucleosome
positioning in vitro is shared by a majority of Alus. We
discovered however, that the specific nucleosome positioning pattern
was disrupted over one member of a young Alu subfamily, which recently
transposed immediately downstream to a T A sequence in the neurofibromatosis type 1 locus (Wallace, M. R.,
Andersen, L. B., Saulino, A. M., Gregory, P. E., Glover, T. W., and
Collins, F. S.(1991) Nature 353, 864-866). Upon removal
of this sequence motif, the expected pattern of assembly was restored
to the neurofibromatosis type 1-Alu template. This finding indicates
that, at least in vitro, certain sequences can override the
propensity for positioning nucleosomes that is inherent to Alu
elements. The finding also raises the possibility that a similar
situation may occur in vivo, with potential implications for
understanding mechanisms by which certain Alu elements may evade
chromatin-mediated transcriptional silencing.

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Copyright © 1996 by the American Society for Biochemistry and Molecular Biology.
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