Monica Ritchie
Genetics
Block E
August 20, 2015
Chapter 1- Question Set # 1
1. An estimated ________ DNA base pairs comprise the human genome.
There are about 3.2 billion DNA base pairs.
2. Define the following:
a) genotype
A genotype is the different allele combination that an individual has that causes a particular trait or disorder. It is the alleles that are present in an individual.
b) phenotype
A phenotype is the visible trait, the allele that is expressed.
c) allele
The different variant of a gene is an allele.
d) mutation
A mutation is when a change in the DNA sequence occurs. Some mutations cause diseases, variations, or no affect at all.
e) genome
A genome is the complete set of genetic instructions of an organism.
Genotype: The make-up of alleles for a particular trait in an organism. For example, if black was a recessive trait in chickens, coded for by b, and there was a black chicken, its genotype would be bb.
1. List whether the student was positive or negative for each characteristic and include whether the characteristic is dominant or recessive. (6 points)
C. A chromatid is a chromosome that has been replicated but has not yet separated from its sister chromatid.
Nitrogenous bases can either be A, G, C, or T. These letters are significant because when they are put into certain orders, form different instructions and form different sets of rules. A stands for adenine, G stands for guanine, C stands for cytosine, and T stands for thymine. All of these nucleotides make up the double helix that is the main structure of DNA. A mutation is a natural process that changes and substitutes a DNA’s sequence of codons and bases. The order of the codons is crucial because, as stated above, directly relate to the instructions that are written for specific parts of the human. The most common form of a mutation is a single base being substituted for another. But mutations are not always negative. Mutation generates new variations that can give an individual a survival advantage (Health Sciences). A healthy gene is different from a mutated gene because a healthy gene has information that fits in the specific human body. A mutated gene is a gene that has information that is distorted, and will contribute differently during the process if creating a human. As an example, during protein synthesis, there can be point mutations, which leads to deformed red blood cells in sickle cell disease. In Tay Sachs disease, the mutated gene leads to raised toxic levels in the spinal cord and the brain (Health Sciences). Overall, the idea of the structure of DNA and the idea of mutations help to explain genetic disorders because both are involved in making
1. A genetic mutation gene is a gene that is passed from family member to family member; There are two types of these genes and one is called BRACA
Mutations happen to many organisms. I for one am a mutation. A mutation is when a gene that is added or detached from the DNA sequence. For example my mutation happened in my eyes one of the genes detached or stopped
In 1831, Charles Darwin, proposed a theory of evolution occurring by the process of natural selection. This has come to be known as the Theory of Natural Selection. Darwin worked on his theory for 20 years and after learning that Alfred Russel Wallace, another naturalist, had developed similar ideas, the two made a joint announcement of their discovery in 1858. Darwin published 'On the Origin of Species by Means of Natural Selection' in 1859, 28 years after he proposed his theory of natural selection. [1]
In order to descry the term mutation, it is crucial to grasp the definition of the word error. According the Merriam-Webster, error is “a deficiency or imperfection in structure or function.” Errors are mistakes; mistakes in nature occur in the formations of nucleotides, which is what makes up DNA. As stated by journalist, Rachel Rettner, nucleotides are composed of “four types of nitrogen bases,” which include: “adenine (A), thymine (T), guanine (G) and cytosine (C).” The sequence of the bases manipulates the instructions of DNA, and changes the genetic codes. When genetic codes are introduced to random influences an error occurs in the DNA formation and causes new recessive genes; these genes are called mutations. Mutation are a genetic error,
Phenotypes driven by DNA from passing of traits from parent to offspring. Before children are born, they receive half of their traits from their mother and the other half from their father. That is why the child may have their father’s nose and their mother’s eye shape. Other traits could include eye color, hair color, hair texture, weight, and skin color. Different combinations of traits may cause offspring to appear different from their parents. However, the majority of traits inherited from parents will be the same. There are other things that you do not inherit from parent inherited traits. These are traits that from what the offspring learn or are caused by the environment. Phenotypes is expressed in part through the processes of transcription and translation. In transcription, the cell copies the gene
Genotype is the genetic information included in the DNA of a living thing. (Page 197)
Mutation rate is the amount of the rate at which different types of mutations happen over time. The rate of replacements can be additional sectioned into a mutation spectrum which describes the effect of genetic context on the mutation rate. The mutation rate of an organism is a progressed characteristic and is strongly affected by the genetics of each organism, also including strong influence from the environment.
According to biology-online.org, genotypes are defined as, “The entire set of genes in an organism… A set of alleles that determines the expression of a particular characteristic or trait.” A genotype is an organism’s Genetic make-up. A human’s genetic code is unique to each individual, a blueprint that is provided by the parents. “The genotype of an organism is the class to which that organism belongs as determined by the description of the actual physical material made up of DNA that was passed to the organism by its parents
Each organism, cell or individual receives a pair of chromosomes from each one of the parents during development. Alleles are the genes found inside the chromosomes and consist of numerous variations such as eye color and hair color as well as many other variations. The alleles aid in the genetic makeup of a cell, organism or individual. The genetic makeup is referred to as genotype and may carry dominant or recessive genes as well as certain diseases. An individual’s limitations and hereditary character are determined by the genotype. A genotype is responsible for determining which traits are developed in an individual and play a huge role in developing an individual’s phenotype.
“A genetic disease or disorder is the result of changes, or mutations, in an individual’s DNA. A mutation is a change in the DNA sequence that make up a gene” When a gene is mutated or is not present, its protein product can no longer carry out its normal function, and thus disorder or genetically inherited disease can occur.
To begin with, mutations (any change in the DNA sequence of an organism) introduce new genetic information into a population by altering alleles (a form of a gene usually arising through mutation) that are already present. Occasionally, a mutation introduces a new allele into the gene pool of species. On the other hand, a mutation may introduce an allele that was deficient in a local population. Meanwhile, it is present in other populations of species. All the different