Star is a brilliantly glowing sphere of hot gas whose energyis produced by an internalnuclear fusion process. Stars are contained in galaxies. A galaxy contains not only stars, but clouds of gas and dust. These clouds are callednebulae, and it is in a nebula where stars are born. In the nebula is hydrogen gas which is pulled together by gravityand starts to spin faster. Over millions of years, more hydrogen gas is pulled into the spinning cloud. The collisions which occur between the hydrogen atoms starts to heat the gas in the cloud. Once the temperature reaches 15,000,000 degrees Celsius, nuclear fusion takes place in the center, or core, of the cloud. The tremendous heat given off by the nuclear fusion process causes the gas to glow creating a protostar. This is the first step in the evolution of a star. The glowing protostar continues to accumulate mass. The amount of mass it can accumulate is determined by the amount ofmatter available in the nebula. Once its mass is stabilized, the star is known as a main sequence star. The new star will continue to glow for millions or even billions of years. As it glows, hydrogen is converted into helium in the core by nuclear fusion. The core starts to become unstable and it starts to contract. The outer shell of the star, which is still mostly hydrogen, starts to expand. As it expands, it cools and starts to glow red. The star has now reached the red giant phase. It is red because it is cooler than the protostar phase and it is a giant because the outer shell has expanded outward. All stars evolve the same way up to the red giant phase. The amount of mass a star has determines which of the following life cycle paths the star will take.
Answer:
genomic imprinting
Explanation:
Genomic imprinting is a mechanism for regulating gene expression that allows expression of only one of the parental alleles, although both alleles are functional. Unlike most genes in which expression is biallelic, genes that are subjected to this mechanism (imprinted genes) have monoalelic expression; By definition, in an imprinted loci, only one allele is active (maternal or paternal), and the inactive is epigenetically marked by histonic modification and / or methylation of cytosines.
Genomic imprinting can cause some disturbances, among them Prader-Willi syndrome, which is a genetic disorder that involves a partial deletion of chromosome 15q on the paternal chromosome.
Pure and accurately labeled.
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