Biology 2581B Chapter Notes - Chapter 8: G1 Phase, G2 Phase, Asexual Reproduction

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3 May 2020

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The transmission of traits from one generation to the next. The scientific study of heredity and hereditary variation. Hereditary units with dna which program different traits. All cells in the body except gametes (46 chromosomes, 23 pairs) Asexual reproduction: a single individual is the sole parent and passes copies of all its genes to its offspring without the fusion of gametes. A gene"s specific location along the length of a chromosome: mitotic cell division, daughter cells which are exact genetic copies of the mother cell, cloning/budding, genetic difference occur due to mutations. Sexual reproduction: two parents give rise to offspring that have unique combinations of genes inherited from the parents: offspring varies genetically from parents and siblings, meiotic cell division and fertilization. An ordered display of one"s chromosomes in homologous pairs. Chromosomes with the same length, centromere position and staining pattern. They carry genes controlling the same inherited characters.

Related Questions

Question 1 (2 points)

In which phase of cell division is marked by the dissolution of the nuclear membrane, the condensation of chromosomes, and the formation of the mitotic spindle?

Question 1 options:

	prophase
	metaphase
	telophase
	anaphase

Question 2 (2 points)

The physical separation of cells during cell division is called:

Question 2 options:

	Cytokinesis
	Telophase
	Interphase
	Chromosome
	Cell plate

Question 3 (2 points)

Meiosis is necessary for sexual reproduction; the gametes formed during this process before fertilization are _______________.

Question 3 options:

	Haploid
	Diploid
	Zygote
	Homologous
	Tetrads

Question 4 (2 points)

Mitosis is the process by which a ___________ cell separates the chromosomes in its nucleus into two identical sets of nuclei.

Question 4 options:

	eukaryotic
	prokaryotic
	bacterial
	all of these are correct

Question 5 (2 points)

Which of the following statements about crossing over is INCORRECT?

Question 5 options:

	It occurs between homologous chromosomes
	It allows for two parents to produce many different types of offspring
	It contributes to genetic diversity in a population
	It occurs during prophase I of mitosis

Which statements pertaining to genetic variability are correct? Check all that apply (note that wrong answers will be deducted from right answers)!

Crossing over is defined by the exchange of chromosome pieces during metaphase one of meiosis.

If a germ cell (i.e. parent cell before meiosis) had only two pairs of homologous chromosomes (i.e. 4 chromosomes total) there are 2 possible combinations of maternal and paternal chromosomes in gametes.

Siblings produced by sexual reproduction are different because sperms are different from one another and eggs are different from one another, and the combination of an egg and sperm is basically unique.

Random fertilization means that all possible combinations of eggs and sperm are equally likely, i.e. it is pure chance which sperm fuses with which egg.

Individual chromosomes contain thousands of genes. This means that during each crossing over event, more than one gene is exchanged between paternal and maternal chromosomes.

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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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Biology 2581B Chapter Notes - Chapter 8: G1 Phase, G2 Phase, Asexual Reproduction

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