islands are normally heavily methylated. However, this can be reversed by treating cells with 5Azacytidine (5’azaC). First studied in 1979 by fellow USC researchers, 5’azaC is an FDAapproved chemotherapeutic agent that is also a DNA methylation inhibitor [4]. By forcing…
islands are normally heavily methylated. However, this can be reversed by treating cells with 5Azacytidine (5’azaC). First studied in 1979 by fellow USC researchers, 5’azaC is an FDAapproved chemotherapeutic agent that is also a DNA methylation inhibitor [4]. By forcing…
Matt is a history teacher. His twin brother Greg is a drug addict. Growing up in the Boston area, both boys did well in high school: they were strong students in the classroom and decent athletes on the field, and they got along with their peers. Like many young people, the brothers drank the occasional beer, smoked cigarettes and experimented with marijuana. Then, in college, they tried cocaine. For Greg, the experience derailed his life. The questions that have risen from this are: what made Greg so susceptible to the grasps of cocaine- to the point that the drug essentially destroyed his life? And how did his identical twin, who shares the exact same genes, escape a similar fate? And how can exposure to a drug set up some individuals for a lifelong addiction, while others can move past their youthful indiscretions and go on to lead productive lives? These questions, although not new, have lead neuroscientist to begin taking a fresh approach to finding the answers. New findings suggest that experience can contribute to mental illness by adding or removing “epigenetic” marks on chromosomes. These tags are particular chemicals that can influence gene activity without changing the information encoded in the gene.…
4. Epistasis: When a gene at one locus alters the phenotypic expression of a gene at a second locus…
The field of epigenetics is “the study of heritable changes in gene activity which are not caused by changes in the DNA sequence” (“Wikipedia”; n.d.). One can adopt a healthy lifestyle to change the impact of the genes inherited by an offspring. Ornish states that changing eating habits, loving more, and getting more exercise can cause a large increase in brain cells. (“ted.com/speakers”; n.d.) These changes could also impact the number of disease provoking genes that one will pass on to an offspring.…
Genetic inheritance was thought to have involve the transmission of DNA from one generation to the next affected by occasional mutations in the DNA itself. They found out that the human genome was less complex and had less genes then even less complex organisms such as plants. The human genome, only containing about 30,000 genes, now lead scientists to believe that other factors allow genes to be switched on and off in response to the environment. Professor Pembrey was drawn to two genetic diseases due to families exhibiting unconventional genetic inheritance patterns. The two diseases were Angelman syndrome, which displays clinical symptoms of jerky movements, little or no speech and a very happy personality, and Prader-Willi syndrome, in which patients are found to be very floppy in infancy and develop an insatiable appetite associated with obesity in later life. He found out that these two diseases were caused by the same genetic alteration. There was a small deletion on chromosome 15. The parent from whom the mutation was inherited determined which disease the patient would get. If it was inherited from the mother the child would have Angelman syndrome and if it was inherited from the father the child would have Prader-Willi syndrome. This suggested that the chromosome knew its origin and must had been tagged or imprinted in some way. This was known as genomic imprinting. During sperm and egg production(meiosis), a chemical change results in the same DNA sequence on each chromosome having different functional properties. These events can lead to a particular gene being turned on or off. This is what epigenetics is based of. Professor Reik noticed that when a mouse embryo was placed in a culture dish some of genes would be switched off and wondered whether this could also be true for human embryos during in vitro fertilization or IVF. Using the disease, Beckwith-Wiedeman syndrome, Reik discovered that Beckwith-Wiedeman syndrome occurs…
* 1) A majority of genetically engineered crops in production worldwide today have been engineered with a gene that:…
DNA in the nucleus is loose and not well defined into chromosomes because it is usually tightly coiled, but in the interphase nucleus the chromatin exists in two forms: loosely coiled form called euchromatin and tightly coiled formed called heterochromatin. These two types become more coiled to form the chromosome at the time of cell division. DNA is a bit loosely coiled in the euchromatin its bases are then available for transcription. When it is in the form of heterochromatin, the bases are not accessible for reading by RNA polymerase hence transcription is not possible as majority of genes must be transcribed in the nucleus so the chromosomes must be decondesed to appear in the form of chromatin and that too in form of euchromatin if DNA remained organized in the sense that they would not be accessible for transcription.…
The influence of nonrandom mating on the distribution of genotypes among a group of animals.…
DNA consists of two polynucleotide chains and these nucleotides consist of a deoxyribose sugar, a nitrogenous base and a phosphate group. The bases are Adenine, Cytosine, Guanine and Thymine. The sequence of these bases on DNA determines the structure of these proteins. A gene is a sequence of bases which codes for a single polypeptide. Chromosomes carry these genes and these genes come in specific forms called an allele which is how living organisms vary from each other. For example, humans are made up of an XY or XX chromosome. Females are XX and males are XY, however in some animals their sex is determined by the ZW sex-determination…
References: 1. Zhang, Yu-Wen, Kyle A. Furge, Ben Staal, Karl J. Dykema, and George F. Vande Woude. "PLOS ONE: Cancer-Type Regulation of MIG-6 Expression by Inhibitors of Methylation and Histone Deacetylation." PLOS ONE: accelerating the publication of peer-reviewed science. N.p., n.d. Web. 6 Oct. 2013. .…
S. L. Berger, T. Kouzarides, R. Shiekhattar, A. Shilartifard. (2009) An operational defintion of epigenetics. Genes Dev. 23: 781-78.3. Available at: http://genesdev.cshlp.org/content/23/7/781.full.pdf+html…
Those that experience post-traumatic stress disorder (PTSD) know that it’s a horrible experience, one that they wouldn’t want to pass on. For those who experienced PTSD provoking trauma it’s a sad reality that their PTSD will be passed on to their children who didn’t experience the traumatic event, creating a cycle. PTSD, among other things, has the ability to be passed down because of epigenetics, the study of changes in organisms caused by modification of gene expression rather than alteration of the genetic code itself. Epigenetics is a widely debated topic because it states that children’s genes are negatively changed because of their parents’ trauma. Some critics argue that people with anxiety and health complaints are more aware of their…
Non-coding DNA influences the activity of other genes, which could cause mutations. Due to the fact that the Human Genome Project gets bigger by the year and new information is updated almost daily, it will be easier to find any potential diseases caused by variables of the non-coding regions of the genome (Source G). The greatest genetic disturbance is caused when the “ultrasensitive” regions are altered. When major parts of the genome is not translated by the non-coding DNA, mutations occur (Source F). An international group of cancer researchers completed a study that found out that mutated non-coding DNA molecules can in fact cause cancer (Source E). A team of scientists applied a computer they developed, FunSeq, to more than 80 genomes and found approximately 100 potential non-coding cancer variants (Source G). Evidence has been found that Non-coding DNA moulds and shaped mice’s skull. The same Non-coding DNA is found in humans, and could mean that it also moulds human skulls (Source D). According to a scientist, Wray, research has shown that diseases such as bipolar and depression may be associated with mutations of the non-coding region that determines whether the brain is producing enough of a particular neurotransmitter or not (Source…
The literature has shown that spirituality (e.g. holiness, hope, love, faith, mindful meditation), emotional (joy, love, pleasure), intellectual, physical (diet, physical activity), environment factors lead to positive epigenetic changes (e.g. DNA methylation, histone modification, non codingRNA) in the body1. Various randomized trials on the body (physical activity, diet, sleep, reduce consumption of alcohol and cigarette) mind (love, joy, meditation), and spirit (prayer, meditation, hope, faith) shows positive epigenetic changes such as telomere perpetuation, and apoptotic regulation, which helps to improve inflammatory response and immune system and also helpful in the treatment of various diseases such as irritable bowel syndrome, hypertension,…