Chapter 12: Problem 7
What chemical and structural properties of histones enable them to successfully package eukaryotic DNA? What is chromatin remodeling, and how is it controlled within eukaryotic cells?
Chapter 12: Problem 7
What chemical and structural properties of histones enable them to successfully package eukaryotic DNA? What is chromatin remodeling, and how is it controlled within eukaryotic cells?
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Get started for freeWhat genetic process is occurring in a puff of a polytene chromosome? How do we know this experimentally?
Cancer can be defined as an abnormal proliferation of cells that defy the normal regulatory controls observed by normal cells. Recently, histone deacetylation therapies have been attempted in the treatment of certain cancers (reviewed by Delcuve et al., 2009 ). Specifically, the FDA has approved histone deacetylation (HDAC) inhibitors for the treatment of cutaneous T-cell lymphoma. Explain why histone acetylation might be associated with cancer and what the rationale is for the use of HDAC inhibitors in the treatment of certain forms of cancer.
A number of recent studies have determined that disease pathogenesis, whether it be related to viruses, cancer, aging, or a host of other causes, is often associated with specific changes in DNA methylation. If such patterns are to be considered as biomarkers for disease diagnosis what requisite criteria would you consider essential to their use?
Variable number tandem repeats (VNTRs) are repeating DNA sequences of about 15 to 100 bp in length, found both within and between genes. Why are they commonly used in forensics?
Examples of histone modifications are acetylation (by histone acetyltransferase, or HAT), which is often linked to gene activation, and deacetylation (by histone deacetylases, or HDACs), which often leads to gene silencing typical of heterochromatin. Such heterochromatinization is initiated from a nucleation site and spreads bidirectionally until encountering boundaries that delimit the silenced areas. Recall from earlier in the text (see Chapter 4 ) the brief discussion of position effect, where repositioning of the \(w^{+}\) allele in Drosophila by translocation or inversion near heterochromatin produces intermittent \(w^{+}\) activity. In the heterozygous state \(\left(w^{+} / w\right),\) a variegated eye is produced, with white and red patches. How might one explain position-effect variegation in terms of histone acetylation and/or deacetylation?
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