Remodeling your home with a reasonable budget PBL Project 2014-2015
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Remodeling your home with a reasonable budget PBL Project 2014-2015 - Video

Chromatin remodeling is the dynamic modification of chromatin architecture to allow access of condensed genomic DNA to the regulatory transcription machinery proteins, and thereby control gene expression. Such remodeling is principally carried out by 1) covalent histone modifications by specific enzymes, i.e., histone acetyltransferases (HATs), deacetylases, methyltransferases, and kinases, and 2) ATP-dependent chromatin remodeling complexes which either move, eject or restructure nucleosomes.[1] Besides actively regulating gene expression, dynamic remodeling of chromatin imparts an epigenetic regulatory role in several key biological processes, e.g., DNA replication and repair; apoptosis; chromosome segregation as well as development and pluripotency. Aberrations in chromatin remodeling proteins are found to be associated with human diseases, including cancer. Targeting chromatin remodeling pathways is currently evolving as a major therapeutic strategy in the treatment of several cancers.

The transcriptional regulation of the genome is controlled primarily at the preinitiation stage by binding of the core transcriptional machinery proteins (namely, RNA polymerase, transcription factors, and activators and repressors) to the core promoter sequence on the coding region of the DNA. However, DNA is tightly packaged in the nucleus with the help of packaging proteins, chiefly histone proteins to form repeating units of nucleosomes which further bundle together to form condensed chromatin structure. Such condensed structure occludes many DNA regulatory regions, not allowing them to interact with transcriptional machinery proteins and regulate gene expression. To overcome this issue and allow dynamic access to condensed DNA, a process known as chromatin remodeling alters nucleosome architecture to expose or hide regions of DNA for transcriptional regulation.

By definition, chromatin remodeling is the enzyme-assisted process to facilitate access of nucleosomal DNA by remodeling the structure, composition and positioning of nucleosomes.

Access to nucleosomal DNA is governed by two major classes of protein complexes:

Specific protein complexes, known as histone-modifying complexes catalyze addition or removal of various chemical elements on histones. These enzymatic modifications include acetylation, methylation, phosphorylation, and ubiquitination and primarily occur at N-terminal histone tails. Such modifications affect the binding affinity between histones and DNA, and thus loosening and tightening the condensed DNA wrapped around histones, e.g., Methylation of specific lysine residues in H3 and H4 causes further condensation of DNA around histones, and thereby preventing binding of transcription factors to the DNA leading to gene repression. On contrary, histone acetylation relaxes chromatin condensation and exposes DNA for TF binding, leading to increase gene expression.[2]

Well characterized modifications to histones include:[3]

Both lysine and arginine residues are known to be methylated. Methylated lysines are the best understood marks of the histone code, as specific methylated lysine match well with gene expression states. Methylation of lysines H3K4 and H3K36 is correlated with transcriptional activation while demethylation of H3K4 is correlated with silencing of the genomic region. Methylation of lysines H3K9 and H3K27 is correlated with transcriptional repression.[4] Particularly, H3K9me3 is highly correlated with constitutive heterochromatin.[5]

Acetylation tends to define the openness of chromatin as acetylated histones cannot pack as well together as deacetylated histones.

However there are many more histone modifications, and sensitive mass spectrometry approaches have recently greatly expanded the catalog.[6]

The histone code is a hypothesis that the transcription of genetic information encoded in DNA is in part regulated by chemical modifications to histone proteins, primarily on their unstructured ends. Together with similar modifications such as DNA methylation it is part of the epigenetic code.

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Chromatin remodeling - Wikipedia, the free encyclopedia

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Home Remodeling Ideas To Boost The Value Of Your Property
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How to Strengthen Garage Ceiling for Storage Home Remodeling
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Here are plans from developer Steve Zemo to remodel part of the Copps Hill Commons complex at 109 Danbury Road. Construction is scheduled to begin early in January.

Getting fit in the new year is a popular resolution and it may be a little easier in 2015, thanks to renovation plans at 109 Danbury Road, a part of the Copps Hill Commons marketplace, that are set to begin on Jan. 2.

Our main goal is to remarket this space to make it more of an extension of the healthy living style on the upper level, said owner Steve Zemo.

Physically, the buildings lower level west faade that faces Kohls will receive elevated signage as well as new dormers and windows.

The building isnt going to be any higher, but the improvements will give an illusion that it is higher, Mr. Zemo said.

Were not adding any additional footage; were just trying to make it look more visually appealing, he said.

Commercially, the outside changes, along with major renovations to the inside space, will create opportunities for new businesses two to three, according to Mr. Zemo to join the 6,500-square-foot complex.

The new businesses will have to meet a certain requirement.

They will have to be complementary to the health and wellness lifestyle that we are trying to promote there, Mr. Zemo said.

Its had a fitness use since 1986, and the current business, The Fitness Studio, is relocating, but we really want to build off of that track record of having some sort of physical activity in that spot, he said.

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Remodeling Copps Hill starts in January

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