Professor Dilek Sanver-Wang 

:
Dilek Sanver-Wang, MS
Instructor, Life Sciences
E-mail:sanverd@lamission.edu
 
 

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LAMC
BIOLOGY

 

Bio3: Midterm 3 Study Guide - Fall 2006

Topics:

The midterm will cover the lecture topics for chapters 8-10.
- mitosis and meiosis
- genetics (Punnett squares, test cross, sex-linked genes, etc.)
- inheritance patterns
- structure of DNA and RNA
- processes of transcription and translation

1. Which one of the following is a difference between sexual and asexual reproduction?
a. Cell division only occurs after sexual reproduction.
b. Only offspring from asexual reproduction inherit traits from two parents.
c. Sexual reproduction typically includes the development of unfertilized eggs.
d. Sexual reproduction is more likely to increase genetic variation than is asexual reproduction.
e. Only asexual reproduction results from the union of a sperm and an egg.

2. Which one of the following is FALSE?
a. Prokaryotic chromosomes are more complex than those of eukaryotes.
b. Most prokaryotes reproduce by binary fission.
c. Prokaryotic cells are generally smaller and simpler than eukaryotic cells.
d. In prokaryotes, most genes are carried on a circular DNA molecule.
e. Daughter prokaryotic chromosomes are separated by some sort of active movement away from each other and the growth of new plasma membrane between them.

3. The process by which the cytoplasm of a eukaryotic cell divides to produce two cells is called:
a. interphase.
b. cytokinesis.
c. metaphase.
d. anaphase.
e. prophase.

4. Which of the following occurs during interphase?
a. condensing of the chromosomes
b. duplication of the chromosomes
c. separation of chromosomes
d. cytokinesis
e. lining up of chromosome along the center of the cell

5. When animal cells are grown in a petri dish, they typically stop dividing once they have formed a single, unbroken layer on the bottom of the dish. This arrest of division is an example of:
a. cancer.
b. cell constraint.
c. density-dependent inhibition.
d. cell division repression.
e. growth factor desensitization.

6. Which one of the following is NOT a function of mitosis? Mitosis helps organisms
a. grow.
b. regenerate lost parts.
c. reproduce asexually.
d. repair tissues.
e. All of the choices are correct.

7. Which of the following statements is FALSE?
a. Meiosis only occurs in the ovaries and testes.
b. All sexual life cycles involve an alternation of diploid and haploid stages.
c. Mitosis produces daughter cells with half the number of chromosomes as the parent cell.
d. A normal human zygote has 46 chromosomes (23 pairs).
e. A haploid cell has half the chromosomes of a diploid cell.

8. During which stage of meiosis do synapsis and the formation of tetrads occur?
a. interphase I
b. prophase I
c. interphase II
d. prophase II

9. Independent orientation of chromosomes at metaphase I results in an increase in the number of:
a. gametes.
b. homologous chromosomes.
c. possible combinations of characteristics.
d. sex chromosomes.
e. points of crossing over.

10. If a chromosome fragment breaks off and then reattaches to the original chromosome but in the reverse direction, the resulting chromosomal abnormality is called a(n):
a. deletion.
b. inversion.
c. translocation.
d. nondisjunction.
e. reciprocal translocation.

11. Mendel conducted his most memorable experiments on:
a. peas.
b. roses.
c. guinea pigs.
d. fruit flies.
e. clones.

12. Which one of the following is FALSE?
a. The genetic makeup of an organism constitutes its genotype.
b. An organism with two different alleles for a single trait is said to be heterozygous.
c. Alleles are alternate forms of a gene.
d. An allele that is fully expressed is referred to as recessive.
e. The expressed physical traits of an organism are called its phenotype.

13. A carrier of a genetic disorder who does not show symptoms is most likely to be __________ to transmit it to offspring.
a. heterozygous for the trait and able
b. heterozygous for the trait and unable
c. homozygous for the trait and able 
d. homozygous for the trait and unable

14. Imagine that beak color in a finch species is controlled by a single gene. You mate a finch homozygous for orange (pigmented) beak with a finch homozygous for ivory (unpigmented) beak and get numerous offspring, all of which have a pale, light orange beak. This pattern of color expression is most likely to be an example of:
a. incomplete dominance.
b. codominance.
c. pleiotropy.
d. polygenic inheritance.
e. crossing over.

15. A person with AB blood illustrates the principle of:
a. incomplete dominance.
b.
blending inheritance.
c. pleiotropy.
d. polygenic inheritance.
e. codominance.

16. How many sex chromosomes are in a human gamete?
a. one
b. two
c. three
d. four
e. five

17. Any gene located on a sex chromosome:
a. is called a recessive gene.
b. is called a dominant allele.
c. is called a sex-linked gene.
d. will exhibit pleiotropy.
e. will exhibit codominance.

18. Explain the difference between complete dominance, codominance and incomplete dominance.  Give an example of each type of inheritance pattern.

19. You conduct a cross between two flowers for flower color. If the genotypes of the parent flowers are: Pp x Pp, what are resulting genotypes and their proportions in the offspring? 
(Note: Purple (P) is dominant and white (p) is recessive)
 

20. You conduct a cross between two flowers for flower color and plant height. If the genotypes of the parent flowers are: ppTt x PpTt, what are resulting phenotypes and their proportions in the offspring? 
(Note: Purple (P) is dominant and white (p) is recessive; tall (T) is dominant and short (t) is recessive)
 

21. Color blindness is a recessive sex-linked trait.  A color-blind woman marries a man with normal vision.  Can this couple have a color-blind daughter?  Why or why not? (Note: N= normal vision; n= color-blindness)

22. The monomers of DNA and RNA are:
a. amino acids.
b. monosaccharides.
c. nucleotides.
d. fatty acids.
e. triglycerides.

23. Which of these is always true with regard to a DNA double helix?
a. The amount of adenine is equal to the amount of uracil, and the amount of guanine is equal to the amount of cytosine.
b. The amount of adenine is equal to the amount of thymine, and the amount of guanine is equal to the amount of uracil.
c. The amount of adenine is equal to the amount of guanine, and the amount of thymine is equal to the amount of cytosine.
d. The amount of adenine is equal to the amount of cytosine, and the amount of guanine is equal to the amount of thymine.
e. The amount of adenine is equal to the amount of thymine, and the amount of guanine is equal to the amount of cytosine.

24. The shape of a DNA molecule is most like:
a. a set of railroad tracks.
b. a diamond ring.
c. a twisted rope ladder.
d. a gold necklace.
e. the letter X.

25. Experiments have demonstrated that the "words" of the genetic code (the units that specify amino acids) are:
a. single nucleotides.
b. two-nucleotide sequences.
c. three-nucleotide sequences.
d. nucleotide sequences of various lengths.
e. enzymes.

26. A base substitution mutation in a gene sometimes does not result in a different protein.  Which of the following factors could account for this?
a. the mutation affects only the sequence of the protein's amino acids, so the protein stays the same
b. the rarity of such mutations
c. a correcting mechanism that is part of the mRNA molecule
d. the fact that such mutations are usually accompanied by a complementary deletion
e. some amino acids are produced from more than one codon

27. Translation consists of which of the following?
a. the conversion of genetic information from the language of nucleic acids to the language of proteins
b. the conversion of genetic information from DNA nucleotides into RNA nucleotides
c. the addition of nucleotides to a DNA template
d. the conversion of genetic information from the language of proteins to the language of enzymes
e. DNA replication

28. Which one of the following best describes the sequence of events of translation?
a. codon recognition → translocation → peptide bond formation → termination
b. peptide bond formation → codon recognition → translocation → termination
c. codon recognition → peptide bond formation → translocation → termination
d. codon recognition → peptide bond formation → termination → translocation
e. peptide bond formation → translocation  → codon recognition → termination

29. Any change in the nucleotide sequence of DNA is called a(n):
a. mutation.
b. advantage.
c. codon.
d. translation.
e. anticodon.

Answers:

1. D                 7. C                  13. A
2. A                 8. B                  14. A
3. B                  9. C                  15. E
4. B                  10. B                16. A
5. C                  11. A               17. C
6. E                  12. D              

18. Complete dominance: the phenotypes of the heterozygote and the dominant homozygote are identical.  Example: any of Mendel’s pea traits.
Incomplete dominance: the heterozygote has an intermediate phenotype Example: pink flower color of the heterozygote in snapdragons and carnations.
Codominance: both alleles are equally expressed in the phenotype of the heterozygote.
Examples: AB blood type in humans; M, N and MN blood group in humans

19.

 

P

p

P

PP

Pp

p

Pp

pp

  Genotypic ratios: ¼ PP, ½ Pp, ¼ pp

20.

 

PT

Pt

pT

pt

pT

PpTT

PpTt

ppTT

ppTt

pt

PpTt

Pptt

ppTT

pptt

Phenotypic ratios: 3/8 purple & tall, 3/8 white & tall, 1/8 purple & short, 1/8 white & short

21. No, because a color-blind daughter would need to have the genotype XnXn so she would need two copies of Xn.  She will inherit one copy from her mother since the mother’s genotype is XnXn, but her father has genotype XNY since he has normal vision.  So the daughter will have genotype XNXn and will have normal vision.

22. C
23. E
24. C
25. C
26. E
27. A
28. C
29. A

 


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Los Angeles, CA USA.  All Rights Reserved.