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Cell cycle and mitosis essay
Cell cycle and mitosis essay
Cell cycle and mitosis essay
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In plant and animal cells there are particular signals that trigger the release of proteins or other regulatory molecules in order to adjust and maintain homeostasis. Not very many molecules can enter, leave, or cross organelle membranes by themselves. Most molecules require the use of transport proteins. Transporter proteins can only bind to very few substrates at a time and undergoes a conformational change so that only these may be transported across the membrane. In order for cell to have normal growth and development cell signaling is a necessity. When a signal molecule binds to a cell surface receptor protein, it activates and releases a G protein on the inside of the cell. The G protein then stimulates adenylyl cyclase to produce large amounts of cyclic AMP with the cell. …show more content…
Mitogen-activated protein (MAP) kinase is a type of catalysis enzyme. Mitogen is a signal that causes cells to undergo mitosis. Since it is a catalysis it will amplify the transduction signal reaction rate across the membrane. MAP kinase cascade involves a series of accessory proteins which then transduces signal from the activated receptor on the cell surface to the regulatory genes in the nucleus. The activated receptor then undergoes phosphorylation. Activated MEK1/2 eventually will activate ERK1/2 which in turn will activate transcription factors of the AP-1 family. The transcription factors now move to the cell nucleus and bind to the AP-1 motif of DNA. The end results activation of transcription a resultant mRNA is transported from nucleus to the
Ligation of EGFP into pET41a(+) vector transformed into E. coli cells followed by PCR amplification of extracted DNA plasmid for success evaluation along with gel electrophoresis at each step.
Overall, as the concentration of the substrate increases, the enzyme activity increases up to a 70% of solution, where the enzyme activity starts to level off. The curve is polynomial because of the fact that the enzyme activity exponentially increases as the concentration of substrate increase; additional evidence for this is the fact that the gradient graph is constantly changing. The polynomial curve is shown because until 70% (the saturation point); this is because there are more casein substrate molecules that can successfully collide with the renin enzyme molecule, therefore increasing the rate of reaction.
to construct and or maintain the cell membrane. In a microscopic view of the cell membrane we can
Receptor tyrosine kinase is a cell membrane receptor system that can trigger multiple cellular responses simultaneously. It requires two receptor tyrosine kinase proteins, which are initially individual polypeptides that each have a signal-binding site, an α helix spanning the cell membrane, and a tail of multiple tyrosines. When signal molecules bind to both proteins they attach through a process called dimerization, forming a dimer. This process activates, or phosphorylates, the ends of the tyrosines, also known as tyrosine-kinase regions. Once the dimer is activated, multiple inactive relay proteins are able to bind to the tyrosine-kinase regions. Each of these proteins trigger a cellul...
This occurs when special carrier proteins carry solutes dissolved in the water across the membrane by using active transport. When the concentration gradient can not allow travel from one side of the membrane to the other fast enough for the cell’s nutritional needs, then facilitated diffusion is used. The transport protein is specialized for the solute it is carrying, just as enzymes are specialized for their substrate. The transport protein can be
Mitochondria are organelles in cells that provide energy, and they have their own DNA. Sometimes, mitochondrial DNA has mutations in it, causing rare, deadly, and incurable diseases. Women who have defective mitochondria can pass these diseases onto their children, but mitochondrial replacement therapy allows these women to have healthy babies that are free from mitochondrial disease.
The direction of osmosis depends on the relative concentration of the solutes on the two sides. In osmosis, water can travel in three different ways. If the molecules outside the cell are lower than the concentration in the cytosol, the solution is said to be hypotonic to the cytosol, in this process, water diffuses into the cell until equilibrium is established. If the molecules outside the cell are higher than the concentration in the cytosol, the solution is said to be hypertonic to the cytosol, in this process, water diffuses out of the cell until equilibrium exists. If the molecules outside and inside the cell are equal, the solution is said to be isotonic to the cytosol, in this process, water diffuses into and out of the cell at equal rates, causing no net movement of water. In osmosis the cell is selectively permeable, meaning that it only allows certain substances to be transferred into and out of the cell. In osmosis, the proteins only on the surface are called peripheral proteins, which form carbohydrate chains whose purpose is used like antennae for communication. Embedded in the peripheral proteins are integral
Proteogenomics is a kind of science field that includes proteomics and genomics. Proteomic consists of protein sequence information and genomic consists of genome sequence information. It is used to annotate whole genome and protein coding genes. Proteomic data provides genome analysis by showing genome annotation and using of peptides that is gained from expressed proteins and it can be used to correct coding regions.Identities of protein coding regions in terms of function and sequence is more important than nucleotide sequences because protein coding genes have more function in a cell than other nucleotide sequences. Genome annotation process includes all experimental and computational stages.These stages can be identification of a gene ,function and structure of a gene and coding region locations.To carry out these processes, ab initio gene prediction methods can be used to predict exon and splice sites. Annotation of protein coding genes is very time consuming process ,therefore gene prediction methods are used for genome annotations. Some web site programs provides these genome annotations such as NCBI and Ensembl. These tools shows sequenced genomes and gives more accurate gene annotations. However, these tools may not explain the presence of a protein. Main idea of proteogenomic methods is to identify peptides in samples by using these tools and also with the help of mass spectrometry.Mass spectrometry searches translation of genome sequences rather than protein database searching. This method also annotate protein protein interactions.MS/MS data searching against translation of genome can determine and identify peptide sequences.Thus genome data can be understood by using genomic and transcriptomic information with this proteogenomic methods and tools. Many of proteomic information can be achieved by gene prediction algorithms, cDNA sequences and comparative genomics. Large proteomic datasets can be gained by peptide mass spectrophotometry for proteogenomics because it uses proteomic data to annotate genome. If there is genome sequence data for an organism or closely related genomes are present,proteogenomic tools can be used. Gained proteogenomic data provides comparing of these data between many related species and shows homology relationships among many species proteins to make annotations with high accuracy.From these studies, proteogenomic data demonstrates frame shifts regions, gene start sites and exon and intron boundaries , alternative splicing sites and its detection , proteolytic sites that is found in proteins, prediction of genes and post translational modification sites for protein.
...e involved in the plants carbohydrate metabolism. This response causes the plant’s cell walls to be rearranged and strengthened. THis would increase the plants resistance to infection and the uptake of harmful chemicals.
The article begins by stating that the tumor suppressor p53 has great importance in the prevention of cancer growth and expansion. Although cancer is the most spoken about topic and p53’s significance against it, p53 also has a hand in ischemia, neurodegeneration, and ageing. While this tumor suppressor seems to be very busy it also regulates the repair of DNA and death of the cell, just to name a few. The activity of p53 can be seen when binding to the DNA at target sequences for transcription. It was pointed out that the doings of p53 are not designated to the nucleus such as other transcription factors as determined over time. Further mentioned in the introduction is a statement that lists this as the most studied mechanism while also related to the material covered in class is apoptosis. P53 inducts apoptosis in the by intrinsic mitochondria-mediated pathway, also transcriptionally through pro-apoptotic parts of the pathway, and in a transcription–independent way which has been recently been looked further into. As if the roles above were not plentiful enough cytoplasmic p53 is also thought to influence autophagy, movement of vesicles, signal transduction, cell metabolism and possibly stem cell expansion, but all are truly determined. Towards the end of the introductory section the authors state that there are still many mechanisms of cytoplasmic p53’s activation leading to apoptosis that are uncertain as well as some p53 missense mutants that lead to oncogenesis. The authors express that the article mainly will speak about the proper or improper activities performed by p53 on the mechanism in the cytoplasm while also looking for areas where beneficial treatments may be used.
Thought to be an oncogene, a gene that has potential in transforming normal cells into tumor cells, p53 was regarded as the most prominent tumor suppressor gene [1]. P53 is a gene which signals apoptosis (programmed cell death) if a cell cannot be repaired due to an extensive amount of damage. As stated in the textbook, p53 regulation occurs by an E3 ubiquitin-protein ligase known as MDM2 [1]. "Controlling the controller" is a statement that describes the molecular interaction where the presence of MDM2 targets the p53 for proteosome via degradation. With three main checkpoints in cell cycle, the literature states p53 functioning from G1 into S phase in a chaotic cell [2]. The normal state of cells is to keep p53 levels low in order to prevent uncontrolled apoptosis and random cell cycle arrest from occurring. In a further note, although p53 promotes apoptosis and cell cycle arrest, cancer may result from p53 unable to recognize the problematic site. In turn, a mutation in p53 may result engaging in new activities. These activities include cellular transformation, tumor metastasis,...
...the activation of MAP kinases (Block et al., 2003). MAPK pathway influence regulation and transformation processes of cell growth (Finkel and Holbrook, 2000). Studies of oxidative stress mechanisms have shown that MAP kinases may be associated with the pathogenesis of diseases related to oxidative stress (Thannickal and Fanburg, 2000).
The implication for this occurrence is that glutamate must block a certain cation-permeable channel keeping the cell continuously depolarized (7). The mGluR6 couples to heterotrimeric G protein complex, known as GO. For phototransduction to occur the GOα ¬ complex must be able close the non-selective melastatin-related transient receptor-1 (TRPM1) cation-channel at the moment when activation of the ON bipolar cell occurs (8). The mechanism of exactly how this complex was able to close the cation-channel was unknown until recently. The dominant α subunit of the G¬O is Gαo and Gαo2 has been noted to help during the ON polar light response (9). Furthermore, Gβϒ in the latest studies in many signaling processes has shown to act differently with different effectors giving array to a multitude of assembly and movement of receptor based signaling complexes (9). Because of Gβϒ there has been signaling mechanisms based on G-proteins range that has increased its
Distinct characteristics are not only an end result of the DNA sequence but also of the cell’s internal system of expression orchestrated by different proteins and RNAs present at a given time. DNA encodes for many possible characteristics, but different types of RNA aided by specialized proteins sometimes with external signals express the needed genes. Control of gene expression is of vital importance for an eukaryote’s survival such as the ability of switching genes on/off in accordance with the changes in the environment (Campbell and Reece, 2008). Of a cell’s entire genome, only 15% will be expressed, and in multicellular organisms the genes active will vary according to their specialization. (Fletcher, Ivor & Winter, 2007).
Cellular transport refers to the movement of compounds across a cell’s plasma membrane. The cell must be able to transport these compounds across the membrane in order to regulate the characteristics of this transport (Reece, 124). The plasma membrane is selectively permeable because of the molecular composition of the plasma membrane, the cell is selective about what comes in and out. (Physio ex 9.1). Cell transport is separated into two distinct aspects: passive transport and active transport. Passive transport refers to the movement of molecules between the interior and exterior of the cell through differences in concentration or pressure gradients. Active transport requires energy known as ATP (Adenosine Tri-phosphate) for the transport to occur.