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Nucleosome assembly on CTG triplet repeats
Author(s): Godde JS, Wolffe AP
Source: JOURNAL OF BIOLOGICAL CHEMISTRY    Volume: 271    Issue: 25    Pages: 15222-15229    Published: JUN 21 1996  
Times Cited: 76     References: 62     
Abstract: Expansion of CTG repeat sequences is associated with several human genetic diseases. We have examined the consequences of CTG repeat expansion for nucleosome assembly and positioning. Short CTG repeats are found within the most favored DNA sequences yet defined for nucleosome assembly. We find that as few as six CTG repeats will facilitate nucleosome assembly to a similar extent as the 50 or more repeats found in disease genes. Thus an increase in nucleosome stability on expansion of existing triplet repeats is unlikely to explain the acquisition of the disease phenotype. However, the CTG repeat sequence is efficiently wrapped around the histone octamer, preferring to associate with histones at the nucleosomal dyad. Thus short segments CTG; repeat sequence will facilitate the assembly of a stable positioned nucleosome which might contribute to the expansion phenomenon and the functional organization of chromatin.
Document Type: Article
Language: English
Reprint Address: Godde, JS (reprint author), NICHHD, MOLEC EMBRYOL LAB, NIH, BETHESDA, MD 20892 USA
Publisher: AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC, 9650 ROCKVILLE PIKE, BETHESDA, MD 20814
Subject Category: Biochemistry & Molecular Biology
IDS Number: UT106
ISSN: 0021-9258
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