Answer:
Of the trillions of cells that compose our body, from neurons that relay signals throughout the brain to immune cells that help defend our bodies from constant external assault, almost every one contains the same 3 billion DNA base pairs that make up the human genome – the entirety of our genetic material. It is remarkable that each of the over 200 cell types in the body interprets this identical information very differently in order to perform the functions necessary to keep us alive. This demonstrates that we need to look beyond the sequence of DNA itself in order to understand how an organism and its cells function.
Explanation:
Our genes can be affected by the environment and change the way our traits are displayed, called the phenotype. However, changes in phenotype have an underlying genotypic source. Epigenetics or epigenetic changes are changes in the way traits are expressed as an effect of the environment (i.e. food we ate, chemicals in the body, environmental stresses), without changes in the DNA. Simply put, in epigenetics, some parts of the DNA are turned on or off in response to environmental conditions.
The addition of an extra nucleotide to a DNA sequence produces a mutation that is called insertion. An insertion mutation can be in various sizes, from one nucleotide base pair to a section of one chromosome inserted into another. When one or more nucleotides are inserted into the genome, the processes of translation and transcription could be disrupted, resulting in altered protein synthesis.
There are 56 neutrons. To find them, you just have to subtract the atomic number with the atomic mass. If you dont know, the atomic number is the number of protons (and electrons) in an atom. The atomic mass is the number of both the protons and neutrons. Of you subtract the atomic number, you get protons.
Answer:
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Explanation:
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