Biology Final Review 1 – Flashcards
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Mendel prevented self-pollination of his plants by
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removing the anthers of the plants.
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The "father" of genetics was
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Gregor Mendel
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Mendel obtained his P generation by allowing the plants to
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self-pollinate
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What is the probability that the offspring of a homozygous dominant individual and a homozygous recessive individual will exhibit the dominant phenotype
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1.0
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True-breeding pea plants always
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produce offspring each of which can have only one form of a trait.
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The first filial (F1) generation is the result of
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crosses between individuals of the parental generation.
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Which of the following is the designation for Mendel's original pure strains of plants?
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P
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F2 : F1 ::
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F1 : P
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The passing of traits from parents to offspring is called
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heredity
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A genetic trait that appears in every generation of offspring is called
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dominant
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homozygous : heterozygous ::
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BB : Bb
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Mendel's finding that the inheritance of one trait had no effect on the inheritance of another became known as the
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law of independent assortment
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To describe how traits can disappear and reappear in a certain pattern from generation to generation, Mendel proposed
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the law of segregation.
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The law of segregation explains that
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alleles of a gene separate from each other during meiosis.
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When Mendel crossed pea plants that differed in two characteristics, such as flower color and plant height,
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he found that the inheritance of one trait did not influence the inheritance of the other trait.
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The phenotype of an organism
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reflects all the traits that are actually expressed.
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If an individual has two recessive alleles for the same trait, the individual is said to be
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homozygous for the trait
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An individual heterozygous for a trait and an individual homozygous recessive for the trait are crossed and produce many offspring. These offspring are likely to be
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of two different phenotypes
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Tallness (T) is dominant over shortness (t) in pea plants. Which of the following represents the genotype of a pea plant that is heterozygous for tallness?
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Tt
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Refer to the illustration in Question 20. The genotype represented in box 1 in the Punnett square would
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be homozygous for freckles.
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Refer to the illustration above. The genotype in box 3 of the Punnett square is
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Ff.
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A trait that occurs in 450 individuals out of a total of 1,800 individuals occurs with a probability of
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0.25
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How many different phenotypes can be produced by a pair of codominant alleles?
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3
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Refer to the illustration above question 24. The phenotype represented by box 1 is
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green, inflated
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Refer to the illustration above question 24. The genotype represented by box 2 is
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GGIi
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2,000 yellow seeds : 8,000 total seeds ::
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1 : 4
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Refer to the illustration above question 27. The device shown, which is used to determine the probable outcome of genetic crosses, is called a
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Punnett square
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Refer to the illustration above question 27. Both of the parents in the cross are
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black
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Refer to the illustration above 27. The phenotype of the offspring indicated by box 3 would be
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black
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Refer to the illustration above 27. The genotypic ratio of the F1 generation would be
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1:2:1
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What is the expected genotypic ratio resulting from a homozygous dominant ´ heterozygous monohybrid cross?
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1:1
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What fraction of the offspring resulting from a heterozygous ´ heterozygous dihybrid cross are homozygous recessive for both traits?
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1/16
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What is the expected genotypic ratio resulting from a heterozygous ´ heterozygous monohybrid cross?
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1:2:1
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What is the expected phenotypic ratio resulting from a homozygous dominant ´ heterozygous monohybrid cross?
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1:0
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efer to the illustration above 35. The phenotype represented by box 1 is
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round, yellow
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Refer to the illustration above 35. The genotype represented by box 2 is
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RrYy
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Refer to the illustration above 35. Which of the following boxes represents the same phenotype as box 7?
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6
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An organism that has inherited two of the same alleles of a gene from its parents is called
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homozygous
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In pea plants, yellow seeds are dominant over green seeds. What would be the expected genotype ratio in a cross between a plant with green seeds and a plant that is heterozygous for seed color?
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1:1
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codominance : both traits are displayed ::
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homozygous : alleles are the same
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The difference between a monohybrid cross and a dihybrid cross is that
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monohybrid crosses involve one trait; dihybrid crosses involve two traits.
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What fraction of the offspring resulting from a heterozygous ´ heterozygous dihybrid cross are heterozygous for both traits?
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1/4
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A cross of two individuals for a single contrasting trait is called
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monohybrid
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Each organism has a unique combination of characteristics encoded in molecules of
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DNA
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The primary function of DNA is to
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store and transmit genetic information
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All of the following are true about the structure of DNA except
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short strands of DNA are contained in chromosomes inside the nucleus of a cell
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Molecules of DNA are composed of long chains of
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nucleotides
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Which of the following is not part of a molecule of DNA?
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ribose
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A nucleotide consists of
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a sugar, a phosphate group, and a nitrogenous base.
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The part of the molecule for which deoxyribonucleic acid is named is the
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sugar
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Refer to the illustration above 51. The entire molecule shown in the diagram is called a(n)
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nucleotide
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Purines and pyrimidines are
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bases found in nucleotides
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The scientists credited with establishing the structure of DNA are
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Watson and Crick
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X-ray diffraction photographs by Wilkins and Franklin suggested that
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DNA molecules are arranged as a tightly coiled helix
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Watson and Crick built models that demonstrated that
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DNA is made of two chains in a double helix
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Chargaff's rules, the base-pairing rules, state that in DNA
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the amount of adenine equals the amount of thymine and the amount of guanine equals the amount of cytosine
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The base-pairing rules state that the following are base pairs in DNA:
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adenine—thymine; guanine—cytosine
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ATTG : TAAC ::
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GTCC : CAGG
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The addition of nucleotides to form a complementary strand of DNA
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is catalyzed by DNA polymerase
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Which of the following is not true about DNA replication?
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The process is catalyzed by enzymes called DNA mutagens
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During DNA replication, a complementary strand of DNA is made for each original DNA strand. Thus, if a portion of the original strand is CCTAGCT, then the new strand will be
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GGATCGA
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The enzymes responsible for adding nucleotides to the exposed DNA template bases are
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DNA polymerases
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The function of tRNA is to
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transfer amino acids to ribosomes
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Which of the following types of RNA carries instructions for making proteins?
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mRNA
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RNA differs from DNA in that RNA
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is sometimes single-stranded.
contains a different sugar molecule
contains the nitrogenous base uracil
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Which of the following is not found in DNA?
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uracil
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RNA is chemically similar to DNA except that its sugars have an additional oxygen atom, and the base thymine is replaced by a structurally similar base called
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uracil
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In RNA molecules, adenine is complementary to
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uracil
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Refer to the illustration above 69. Which of the following is the series of amino acids encoded by the piece of mRNA shown above?
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Leu—Lys—Cys—Phe
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Refer to the illustration above 69. Which of the following would represent the strand of DNA from which the mRNA strand was made?
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GAGTTCACGAAG
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Refer to the illustration above 69. The anticodons for the codons in the mRNA in the diagram are
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GAG—UUC—ACG—AAG
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During translation, a ribosome binds to
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mRNA
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Suppose that you are given a polypeptide sequence containing the following sequence of amino acids: tyrosine, proline, aspartic acid, isoleucine, and cysteine. Use the portion of the genetic code given in the table below 73 to determine the DNA sequence that codes for this polypeptide sequence
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ATGGGTCTATATACG
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Each of the following is a type of RNA except
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carrier RNA
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In order for protein synthesis to occur, mRNA must migrate to the
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ribosomes
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During transcription
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RNA is produced
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Transcription proceeds when RNA polymerase
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binds to a promoter on a strand of DNA
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Transcription is the process by which genetic information encoded in DNA is transferred to a(n)
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RNA molecule
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Each nucleotide triplet in mRNA that specifies a particular amino acid is called a(n)
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codon
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The human genome contains
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30,000 genes.
23 chromosomes.
3.2 billion base pairs.
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During translation, the amino acid detaches from the transfer RNA molecule and attaches to the end of a growing protein chain when
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the transfer RNA anticodon is paired up with the messenger RNA codon
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The transfer of genetic material from one cell to another, which Frederick Griffith studied, is called
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transformation
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Oswald Avery showed that
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cells missing protein and RNA were able to transform R cells into S cells and kill mice, but cells missing DNA could not
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In their experiments, Hershey and Chase used
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DNA labeled with radioactive phosphorus.
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An error in DNA replication can cause
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mutations.
cancer
genetic variation.
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The X and Y chromosomes are called the
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sex chromosomes
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Down syndrome : nondisjunction ::
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male : XY chromosomes
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female : XX ::
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male : XY
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WHAT DOES THIS DESCRIBE???
A female could get the disease only by having a mother who is a carrier and a father who has the disease. Since most males with the disease do not survive to reproductive age, this is an extremely unlikely event.
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hemophilia
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In a mating between two parental types, one of which is homozygous dominant for two linked traits and one of which is homozygous recessive for the same two linked traits, evidence of crossing-over would be apparent in which of the following generations?
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F2
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Which of the following is not true of chromosome maps?
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They depict absolute distances between genes on a chromosome.
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A mutation caused by a piece of DNA breaking away from its chromosome and becoming attached to a nonhomologous chromosome is called
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translocation
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A change in a gene due to damage or incorrect copying is called a
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mutation
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The effects of a mutation can be
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helpful
harmful
neutral
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A diagram in which several generations of a family and the occurrence of certain genetic characteristics are shown is called a
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pedigree
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A family record that indicates the occurrence of a trait is a
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pedigree
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Which of the following traits is controlled by multiple alleles in humans?
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blood type
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What would be the blood type of a person who inherited an A allele from one parent and an O allele from the other?
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type A
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In humans, the risks of passing on a genetic disorder to one's children can be assessed by
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analysis of a pedigree
genetic counseling
prenatal testing
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What
- helps identify parents at risk for having children with genetic defects
-assists parents in deciding whether or not to have children
- uses a family pedigree
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Genetic counseling
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While studying several generations of a particular family, a geneticist observed that a certain disease was found equally in males and females and that all children who had the disease had parents who also had the disease. The gene coding for this disease is probably
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autosomal dominant
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If both parents carry the recessive allele that causes cystic fibrosis, the chance that their child will develop the disease is
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one in four
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If a characteristic is sex-linked, it
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occurs most commonly in males
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Since the allele for colorblindness is located on the X chromosome, colorblindness
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is sex-linked
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People with Down syndrome have how many chromosomes?
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47
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The sex of an offspring is determined by who?
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the father
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If a gamete will receive too many or too few copies of a chromosome, what occurs?
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nondisjunction
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Consider a cross between a homozygous white-eyed female Drosophila and a red-eyed male Drosophila. What proportion of the female offspring would be expected to be white-eyed? What proportion of the male offspring would be expected to be white-eyed?
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none; all