BIOLOGY 1P03 Chapter Notes - Chapter 11 : Quantitative Trait Locus, Hemoglobin, Muscular Dystrophy

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6 Dec 2016

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A recessive hereditary condition caused by defective alleles of the genes that encode the enzymes require for melanin. Carrier: an individual who is heterozygous for a recessive condition; a carrier displays the dominant phenotype but can pass on the recessive allele to offspring. Codominance: the relation between two alleles of a gene, such that both alleles are phenotypically expressed in heterozygous individuals. Cross-fertilization: the union of sperm and egg from two individuals of the same species. Dominant: an allele that can determine the phenotype of heterozygotes completely. Gene linkage: the tendency for genes located on the same chromosome to be inherited together. Genetic recombination: the generation of new combinations of alleles on homologous chromosomes due to the exchange of dna during crossing over. Genotype: the genetic composition of an organism; the actual alleles of each gene carried by the organism. Hemophilia: a recessive, sex-linked disease in which the blood fails to clot normally.

Related Questions

QUESTION 1

Jim is blood type A, his brother John is type O and his sister Jane is type AB. What are the genotypes of their parents?

Which of the following is true for alleles that show incomplete dominance?

Heterozygotes have a genotype like the dominant allele.

Homozygotes have a genotype like the recessive allele.

Heterozygotes have a phenotype intermediate between the dominant and recessive alleles.

Homozygotes have the same phenotype as the heterozygotes.

QUESTION 3

Which principle of inheritance concluded that when games are formed in meiosis, the two alleles of each gene separate from one another, and each gamete receives only one allele?

independent assortment

Which term best describes a condition in which alleles at one locus can alter the expression of alleles at another locus?

polygenic inheritance

A single unit of genetic information located on a chromosome defines:

The physical expression (appearance or function) of an organism's genes defines:

genotype

a single characteristic

Palomino horses (golden color with a blond mane) are an incompletely dominant trait produced by the combination of the chestnut color allele and the cream color allele. If you wanted to produce as many palominos as possible, which mating strategy below would be the best choice?

Which term best describes the effect of a single gene on multiple aspects of the phenotype?

polygenic inheritance

QUESTION 9

Which term best describes the separate expression of both alleles for a single trait in the same cell?

polygenic inheritance

QUESTION 10

One form of a gene found on a single chromosome defines:

A chocolate lab (whose mother was a yellow lab) is mated with a black lab whose genotype is BbEe. What fraction of the offspring would be expected to be yellow labs?

What type of allele is always expressed regardless of whether the individual is homozygous or heterozygous for it?

Both the dominant and recessive alleles

Given the parents AABBGgHhrr Ã AabbGgHhRr, assume simple dominance and independent assortment. What proportion of the progeny will be expected to have the genotype AaBbggHHrr?

___________________ is defined as having two of the same type of allele for a particular trait.

The physical position of an allele on a single chromosome defines:

Which term best describes two or more genes affecting the phenotype in an additive fashion?

codominance

polygenic inheritance

1. A person is described as a carrier for a particular genetic disease. What does this tell you about their genotype?

2. For any given gene, the principle of independent segregation predicts that each gamete produced as a result of meiosis will contain ____________________

3. A pair of alleles is said to be heterozygous when:

4. In a diploid species, cells can have up to ___ alleles of a particular gene.

5. In a cross between a homozygous dominant parent and a homozygous recessive parent, the number of phenotypic classes observed in the offspring is ______

6. For a person of genotype Xx, the genotype of their gametes may be ______________

7. In a "test cross", an individual of unknown genotype is crossed with a ___ individual to determine the unknown genotype.

8. An albino woman has a child with a phenotypically normal man with no family history of albinism (which is a rare recessive disorder). What percentage of their children are likely to be albino?

9. An individual with the dominant phenotype, but an unknown genotype, is test-crossed, and all of the offspring exhibit the dominant phenotype. The genotype of the unknown individual is ______________

10. If two heterozygous individuals for a recessive disease (carriers) have a child, what is the chance that their child will develop the disease?

11. In a monohybrid cross between two true-breeding parents that both exhibit the dominant phenotype, ___ percent of the offspring will exhibit the recessive phenotype.

12. In a particular type of tomato plant, red fruit is dominant over yellow fruit, and dwarf height is a recessive trait. If two heterozygous plants were crossed, what proportion of the offspring would show the dominant phenotype?

13. In a cross between a BbRr individual and a BBRR one, what do the following represent: BR, Br, bR, br?

14. In humans, the gene that determines whether an embryo develops as a male or a female is carried on _____________

amaranthhare726

These all relate to exceptions to the inheritance patterns encountered by Mendel.â

Why do multiple and lethal alleles often result in modifications of the classic Mendelian monohybrid and dihybrid ratios?

Select the four correct statements.

-When an essential gene is mutated, it can result in a lethal phenotype. There are no classic Mendelian monohybrid and dihybrid ratios.

-In the case of codominance, heterozygotes produce gene products from both alleles of a gene. Classic Mendelian monohybrid and dihybrid ratios are modified by codominance.

-In the case of incomplete dominance, the phenotype of the heterozygote is distinct from and often intermediate to the phenotypes of homozygous individuals. Classic Mendelian monohybrid and dihybrid ratios are modified by incomplete dominance.

-Genes exist in a large number of allelic versions and a diploid organism has two homologous gene loci that may be occupied by different alleles of the same gene. This can result in many different phenotypes for traits, which may not follow typical Mendelian ratios.

-When an essential gene is mutated, it can result in a lethal phenotype. This results in a modification of classic Mendelian ratios.

-The phenotype of the heterozygous genotype is distinct from and often intermediate to the phenotypes of the homozygous genotypes. The joint expression of both alleles in a heterozygote is called codominance. There are no classic Mendelian monohybrid and dihybrid ratios.

-Genes exist in a large number of allelic versions, but in a diploid organism, only one allele of the gene can occupy one homologous gene loci. Classic Mendelian inheritance cannot explain this phenomenon.

-Each gene produces a unique gene product. The effect of one allele in a heterozygote completely masks the effect of the other. Classic Mendelian genetics cannot explain this phenomenon.

BIOLOGY 1P03 Chapter Notes - Chapter 11 : Quantitative Trait Locus, Hemoglobin, Muscular Dystrophy

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