[BIOLOGY 2C03] - Final Exam Guide - Ultimate 35 pages long Study Guide!

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orangeferret230

28 Nov 2016

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Genes on the same chromosome that are transmitted together show complete linkage. Morgan studied mutations on x chromosome of d. melanogaster. He observed an incomplete form of linkage, indicated by progeny that exhibited a combination of traits not exhibited in parents. Linkage between genes is usually incomplete because homologous chromosomes can exchange segments when paired (recombination). While alleles present in each chromosome tend to remain together in inheritance, some chromosomes with new combinations of alleles can be transmitted. The probability of crossing over between any two genes is a measure of the genetic distance between the genes. This allows us to construct a genetic map, a diagram of a chromosome showing relative positions of genes. Enables a new gene to be assigned to a schromosome (even to a precise position relative to other genes) It is the first step in identification and isolation of a new gene (useful for identifying genes of hereditary diseases)

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16. Syntenic genes can assort independently when

A) they are very close together on a chromosome.

B) they are located on different chromosomes.

C) crossing over occurs rarely between the genes.

D) they are far apart on a chromosome and crossing over occurs frequently between the genes.

E) they are far apart on a chromosome and crossing over occurs very rarely between the genes.

17. The alleles of linked genes tend to

A) segregate together more often than expected by random assortment

B) assort independently.

C) be mutated more often than unlinked genes.

D) experience a higher rate of crossing over.

E) assort independently and show a higher rate of crossing over.

18. If you know that the frequency of recombination between genes X and Y is 34% and between X and Z is 25%, can you predict the order of the three genes?

A) Yes; the order is X-Z-Y.

B) Yes; the order is X-Y-Z.

C) Yes; the order is Z-X-Y.

D) No; based on this data alone, the order could be Z-Y-X or X-Y-Z.

E) No; based on this data alone, the order could be X-Z-Y or Z-X-Y.

Question 19 - 20. You have performed the following dihybrid cross in Drosophila using the black body color (b) and vestigial wing (vg) mutations. The b+ (grey body) and vg+ (normal wing) are dominant wild type alleles. These genes are autosomal.

Female â b+ vg+/b vg Ã male â b vg/b vg

Progeny:

Phenotype # of Progeny

Grey body normal wing 965

Black body vestigial wing 944

Grey body vestigial wing 208

Black body normal wing 195

19. Assuming linkage between black and vestigial, the estimated recombination frequency would be:

0.17

0.09

0.82

1.00

0.50

20. What key test could you use to determine whether the observed offspring frequencies deviate from those expected by chance alone?

A) Pascal's triangle

B) The product rule

C) The Chi-square (Ï²) test

D) The law of random assortment

E) The sum rule

21. In a genome wide association study (GWAS) designed to map the gene(s) that control height you divide subjects into a group of 1000 who are all more than seven feet tall and a control group of 1000 people of average height. You find the following associations between two genetic markers and the height trait:

		Tall group	Control group
Marker 1	Allele A	20%	50%
	Allele T	80%	50%

Marker 2	Allele G	15%	15%
	Allele C	85%	85%

What is your best guess for which marker is more closely linked to a gene that influences height?

A) Marker 1

B) Marker 2

22. Two pure breeding parents produce red and white flowers. They are crossed and the F1 produces pink flowers. When the F1 are selfed to produce the F2, nine distinct classes of pigmentation are present among F2 individuals. What is your best guess of the minimum number of genes that underlie flower pigmentation in this species?

A. 2

B. 3

C. 4

D. 5

E. 6

23. In a quantitative genetic experiment you identify two genes that confer bands of color on the back of a fly. At each gene, a dominant allele causes one band of color. If flies that are heterozygous at both loci are crossed, what ratio of offspring do you expect in each phenotype (i.e., number of color bands) class? (answer options are given from lowest to highest band number)

A) 1:1:1:1:1

B) 1:2:2:2:1

C) 1:4:6:4:1

D) 4:4:4:4:4

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What is a genome? What is a genome made of? Describe the bacterial genome. How do bacteria reproduce? What is binary fission? Distinguish between a chromosome and chromatin. Where are chromosomes located in eukaryotic cells? What is the chromosome made of? What is a centromere? What is the centromere's role? What are sister chromatids and how do they arise? Distinguish between somatic cells and germ (gametes) cells. Describe the cell cycle. What are the different phases? What occurs during S phase? What is interphase? How is the cell cycle controlled?

Describe mitosis. What are the phases of mitosis? What occurs in each of the phases of mitosis? What is cytokinesis? How does this differ between plant and animal cells? What is a kinetochore? Where does it form? What is its role? What is the role of microtubules in mitosis? What is a centriole and what is it composed of? What is a centrosome and what is its role in mitosis? What is the metaphase plate and why is this important? What is the mitotic spindle, its role and its makeup? What defines a diploid cell? How many copies of each chromosome is in a diploid cell? What about a haploid cell? Why do the daughter cells of mitosis always have the same complement of chromosomes?

Describe meiosis. What are the phases of meiosis? What occurs in each of the phases of meiosis? Distinguish between meiosis I and meiosis II and describe how each of these processes compare to mitosis. Why do animal cells undergo meiosis? What is a gamete? What is a zygote? What are recombination, crossing-over, and chiasma? When and why does this occur? What is meant by 'homologous pair of chromosomes'? Why don't the daughter cells of meiosis have the same genetic makeup? What controls the segregation of chromosomes into the gametes?

What are genetic characters? What are genetic traits? What is an allele? What is a locus? How many alleles at each locus would a human cell have and why? Distinguish between genotype and phenotype. What is meant by a dominant gene? What is meant by a recessive gene? How do these differ? What is the genotype of a homozygous dominant organism? What is its phenotype? What is the genotype of a homozygous recessive organism? What is its phenotype? What is the genotype of a heterozygous organism? What is its phenotype? What is a genetic cross? Distinguish between the P, F1, and F2 generations. What is a true-breeding line? What is the genotype and phenotype of a cross between homozygous dominant and homozygous recessive parents? If the F1 progeny are crossed, what would be the genotype and phenotype of the F2 generation? What would be the phenotypic ratio? What would be the genotypic ratio? Be ready to generate Punnet square tests or probability analyses of crosses involving more than one genetic locus. Describe a dihybrid cross where two alleles are homozygous dominant in one parent and homozygous recessive in the other. What would be the phenotypic ratio of the F2 generation from this dihybrid cross? What is meant by independent assortment? Be prepared to calculate probabilities resulting from different crosses.

Distinguish between complete and incomplete dominance. How would incomplete dominance alter the results of a hybrid cross? What would the resulting F2 generation phenotype and genotype ratios be? What is codominance? How does this affect the results of crosses? Be prepared to determine likely blood types of parents based on the blood types of their offspring. What is a polygenic trait? What is a carrier state for a genetic disease? What is meant by linked genes? How does this affect expected outcomes of genetic crosses? How is gene linkage used for chromosomal mapping? Distinguish between autosomes and sex chromosomes. What sex chromosomes are found in women? What sex chromosomes are found in men? What are sex-linked traits? Be prepared to give the results of crosses that involve sex-linked recessive traits. What is the process of nondisjunction? What are the likely results? Why is this important? What is a Barr body? Recognize the genetic abnormality of Downs Syndrome, Turner's Syndrome, and Klinefelter's Syndrome.

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If an organismâs diploid chromosome number is 18, how many different possible combinations of homologous chromosomes lining up during meiosis exist for the eggs or sperm produced by that organism?

	A.	512
	B.	9
	C.	18
	D.	128
	E.	36

At the end of metaphase I, _______________ separate.

	A.	sister chromatids
	B.	germ cells
	C.	homologous chromosomes
	D.	haploid chromatids
	E.	centrioles

Mendel observed that dominant traits

	A.	are seen in all of the F1 hybrid pea plants in his experiments.
	B.	are expressed in all plants.
	C.	were absent in the F1 generation of pea plants that he used in his experiments.
	D.	were the only traits seen in the F2 generation of pea plants in his experiments.
	E.	are only expressed in hybrids.

Cytokinesis in plant cells differs from cytokinesis in animal cells because

	A.	there is no difference.
	B.	in plant cells, the cell plate must also divide into two parts.
	C.	the contractile protein, actin, is important only in plant cells.
	D.	plant cells have a rigid cell wall.
	E.	a contractile ring forms only in plant cells.

Sickle cell anemia is an example of what type of inheritance?

	A.	complete dominance
	B.	incomplete dominance
	C.	codominance
	D.	multiple alleles
	E.	recessive dominance

Which of the following statements is true:

	A.	The dominant allele is masked in homozygous dominant individuals.
	B.	With recessive genetic disorders, if both parents are carriers, the offspring will all be affected.
	C.	In carriers, the recessive allele causes an intermediate phenotype.
	D.	In recessive genetic disorders, the mother and/or father of an affected individual must also be affected.
	E.	With dominant genetic disorders, the mother and/or father of an affected individual must also be affected.

Skin cancers typically develop in the

	A.	upper layers of the epidermis.
	B.	lower layers of the dermis.
	C.	subcutaneous layer.
	D.	lower layers of the epidermis.
	E.	upper layers of the dermis.

Duchenne muscular dystrophy (MD) is inherited from an X-linked recessive allele. What is the probability that a son with Duchenne MD inherited this disease from his biological father?

	A.	1/2
	B.	0
	C.	1/16
	D.	1/4
	E.	1/8

The genetic makeup of a particular trait in an individual is its

	A.	genotype.
	B.	heterozygosity.
	C.	phenotype.
	D.	filial.
	E.	dominance.

What structure holds the sister chromatids to the spindle fibers?

	A.	chromatin
	B.	kinetochore
	C.	MPF
	D.	centromere
	E.	cyclin

If you view a cell in which the genetic material is beginning to be visible as separate bodies, and the nucleus has disappeared from view, you may surmise that the cells is in

	A.	telophase.
	B.	anaphase.
	C.	interphase.
	D.	metaphase.
	E.	prophase.

Gregor Mendel was successful in his analysis of the genetics of pea plants because

	A.	he examined and analyzed both the F1 and F2 generations.
	B.	he studied the parental plants to determine their differences.
	C.	he decided to only look at his results in an objective manner.
	D.	he studied a trait that had a strange inheritance pattern.
	E.	pea plants have genetics different from other organisms.

Tall corn plants (T) are dominant to dwarf plants (tt). Solid green leaves (G) are dominant to leaves with a white tip (gg). A cross between two corn plants yielded the following phenotypes: 51 tall plants with a white tip on their leaves; 43 dwarf plants with solid leaves; 48 dwarf plants with white tips on their leaves; 45 tall plants with solid leaves. What are the genotypes of the parents that produced these plants?

	A.	None of the above
	B.	TtGg x Ttgg
	C.	ttGG x TTgg
	D.	TtGg x TtGg
	E.	TtGg x ttgg

In humans, a gene that has been identified as causing a type of skin cancer is the

	A.	superwoman echidna.
	B.	mutant superman.
	C.	sonic hedgehog.
	D.	mutant mole rat.
	E.	superhero aardvark.

The segregation principle states that in sexually reproducing diploid organisms the two copies of each gene

	A.	segregate from each other during meiosis.
	B.	must always be the same allele.
	C.	separate from each other during mitosis.
	D.	will both wind up in either the sperm or egg.
	E.	move together as a unit during meiosis.

In what phases is the genetic material in the cell correctly referred to as chromatids?

	A.	metaphase and telophase
	B.	anaphase and metaphase
	C.	interphase and telophase
	D.	interphase and prophase
	E.	metaphase and prophase

Consider two traits for an organism, determined by two genes, each of which is governed by at least two alleles. In the case of a dihybrid individual, the gametes formed will be of either the parental type or the recombinant type. Recombinant type gametes are formed because of

	A.	the principle of dihybrids.
	B.	multiple alleles.
	C.	heterozygosity.
	D.	incomplete dominance.
	E.	independent assortment.

An allele is

	A.	an alternate form of a gene.
	B.	always recessive.
	C.	the main factor determining a trait.
	D.	always one of a pair.
	E.	the dominant form of a gene.

After the DNA is replicated, and it condenses in prophase, two identical rods of DNA are seen. These are

	A.	spindle fibers.
	B.	kinetochores.
	C.	chromatids.
	D.	chromatin.
	E.	centromeres.

Special cells found in the gonads that give rise to gametes upon division are called

	A.	egg cells.
	B.	somatic cells.
	C.	germ cells.
	D.	stem cells.
	E.	basal cells.

[BIOLOGY 2C03] - Final Exam Guide - Ultimate 35 pages long Study Guide!

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