Eukaryotic cells genome

Nakai, K., and Kanehisa, M. (1992). A knowledge base for predicting protein localization sites in eukaryotic cells. Genomics 14, 897-911. 

In the nuclei of all eukaryotic cells, DNA is tightly wrapped around an octamer of histone proteins and is compacted into a dense structure known as chromatin. In order to access the genetic information which is required in numerous essential cellular processes including DNA replication, gene expression and DNA repair, chromatin needs to be partially unwound. One important mechanism to regulate chromatin structure and thus to control the access of the genomic DNA is through histone modifications [1-6]. The histone octamer is composed of two copies of H2A, H2B, H3 and H4 core histone proteins. Their tails, that protrude out of the surface of the... 

Abstract. In eukaryotic cells, replicated DNA molecules remain physically connected from their synthesis in S phase until they are separated during anaphase. This phenomenon, called sister chromatid cohesion, is essential for the temporal separation of DNA replication and mitosis and for the equal separation of the duplicated genome. Recent work has identified a number of chromosomal proteins required for cohesion. In this review we discuss how these proteins may connect sister chromatids and how they are removed from chromosomes to allow sister chromatid separation at the onset of anaphase. 

Hartman, H. and Fedorov, A. (2002). The origin of the eukaryotic cell a genomic investigation. 

The F-box protein family is the largest substrate-recognition subunit family. It enables the eukaryotic cells to use the SCF E3 machinery to ubiquitinate a large number of diverse protein substrates. So far, over 70 F-box proteins have been identified in the human genome [57, 58]. F-box proteins all share an 40-amino acid F-box motif, which is usually followed by a C-terminal protein-protein interaction domain such as the WD40 repeats j5-propeller (Fbw subfamily) and /eucine-rich repeats (LRRs Fbl subfamily Figure 7.5) [59, 60]. F-box proteins interact with... 

Much of industrial chemistry takes place in organic solvents, or involves apolar compounds. Biocatalysis, in contrast, typically involves aqueous environments. Nevertheless, enzymes and microorganisms do in fact encounter apolar environments in Nature. Every cell is surrounded by at least one cell membrane, and more complex eukaryotic cells contain large amounts of intracellular membrane systems. These membranes consist of lipid bilayers into which many proteins are inserted present estimates, based on genomic information, are that about one-third of all proteins are membrane proteins, many of which are so-called intrinsic proteins that are intimately threaded through the apolar bilayer. These proteins are essentially dissolved in, and function partly within, an apolar phase. 

The genome of the eukaryotic cell is packaged in a topologically complex, fibrous superstructure known as chromatin. The nucleosome core particle is the fundamental building block of chromatin and contains 146 bp of DNA wrapped in roughly two super helical turns around an octamer of four core histones (H3, H2B, H2A and H4) resulting in a beads on a string structure. This 10 nm structure further folds and... 

Eukaryotes are differentiated from the Archaea and Eubacteria by the possession of a nucleus in the cell enclosed by a membrane as well as by membrane-enclosed subcellular organelles. The nucleus houses the basic genetic information of these organisms, their genomes, as I will describe in chapter 14. The eukaryotes are a diverse set of species, including but not limited to all plants and animals. Remarkably, the Archaea are more closely related to Eukarya than they are to the Eubacteria. This reflects a striking origin of the eukaryotic cell. 

Ered Sanger, a double Nobel Prize winner, sequenced the human mitochondrial genome back in 1981. This genome codes for 13 proteins and the mitochondrion possesses the genetic machinery needed to synthesize them. Thus, the mitochondria are a secondary site for protein synthesis in eukaryotic cells. It turns out that the 13 proteins coded for by the mitochondrial genome and synthesized in the mitochondria are critically important parts of the complexes of the electron transport chain, the site of ATP synthesis. The nuclear DNA codes for the remainder of the mitochondrial proteins and these are synthesized on ribosomes, and subsequently transported to the mitochondria. 

There are two general kinds of cells those having a membrane-bounded nucleus called eukaryotic cells, and those without a nuclear envelope called prokaryotic cells. Humans have eukaryotic cells. All eukaryotic cells contain a nucleus that contains the genome, the complete set of genes. Unless noted otherwise, our discussion will be restricted to eukaryotic cells. 

Like the mitosome, most organelles in a eukaryotic cell do not possess a genome and translation machinery. Consequently, proteins must be imported to these compartments from the cytosol. Yet the membranes separating these organelles from the cytosol are not freely permeable for large hydrophilic molecules of proteins. As a result, the protein translocation is mediated by membrane transporters in a complex energy-consuming process. The mode of protein translocation across these barriers is typical for each compartment. 

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