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55 Cards in this Set
- Front
- Back
The ___ is the most commonly found in nature. |
Wild-type trait |
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What crosses of allelies will only produce heterozygous offspring? |
AAx aa |
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The backbone of DNA consists of |
A repeating sugar-phosphate-sugar-phosphate pattern |
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The recombination frequency between gene B and gene C is 11%. The recombination frequency between gene B and gene D is 5%. The recombination frequency between gene C and gene D is 15%. What would be the arrangement of these genes on a linkage map? |
DBC |
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In humans, the presence or absence of dimples is a trait controlled by a single gene. What is the genotype of an individual who is heterozygous for dimples |
Dd |
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The correct sequence of stages in mitosis is |
Prophase, Metaphase, Anaphase, Telophase |
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Amanda's abnormal number of sex chromosomes resulted from |
Nondisjunction |
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With respect to her sex chromosomes, Amanda would be designated as |
XO |
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An individual who is homozygous |
Carriers two copies of teh same allele for a gene |
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Janice's genotype is |
WW or Ww |
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Mary has the genotype |
Ww |
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If one strand of a DNA double helix has the sequence GTCCAT, what is the sequence of the other strand? |
CAGGTA |
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How many nucleotides make up a codon? |
Three |
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Who discovered the structure of DNA? |
Watson and Crick |
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The chromosomes of eukaryotic cells are found in the |
Nucleus |
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A mutation within a gene that will insert a premature stop codon in MRNA would |
Result in a shortened polypeptide chain |
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What chromosomes belong to a normal human male? |
44 autosomes, one X chrosome, and one Y chromosome |
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Where is translation accomplished? |
Ribosomes |
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Red-green color blindness is inherited as a sex-linked recessive trait. The gene is found on the X chromosome. How can a man with normal color vision father a daughter who is red-green color-blind? |
He can't (unless there is a mutation) |
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What type of chemical bond joins the bases of complementary DNA strands? |
Hydrogen |
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During metaphas |
Chromosomes line up in the middle of the cell |
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After replication |
Each new DNA double helix consists of one old strand and one new strand |
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Homologous chromosomes
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Carry genes controlling the same inherited characteristics
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A Karyotype (a chromosome display) would be unable to determine |
Eye color |
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A mating between a purebred purple-flowered pea plant and a purebred white-flowered pea plant would produce a(n) |
Hybrid |
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Attached earlobes are recessive to free earlobes. What genotypic ratio is expected when an individual with attached earlobes mates with an individual heterozygous for free earlobes? |
1:1 |
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HIV (human immunodeficiency virus) must use its own ___to reproduce. |
Reverse transcriptase |
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A duplicated chromosome consists of two |
Sister chromatids |
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One difference between mitosis and meiosis is |
Mitosis produces cells genetically identical to the parent cell, but meiosis does not |
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What is the ultimate source of all diversity? |
Mutation |
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What enzyme is responsible for RNA synthesis? |
RNA polymerase |
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If a strand of DNA has the sequence AAGCTC, transcription will result in a(n)
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RNA strand with the sequence UUCGAG
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A purebred plant that produces yellow seeds is crossed with a purebred plant that produces green seeds. The seeds of all the offspring are yellow. Why? |
The yellow allele is dominate to the green allele.
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Alleles are described as |
Alternate versions of a gene |
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What event occurs during anaphase? |
Sister chromatids separate |
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The shape of a DNA molucle is most like |
A twisted rope ladder |
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How can bacteriophage DNA be spread from cell to cell without causing cell death? |
Via a lysogenic cycle |
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The codon AGC codes for the amino acid |
Serine |
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In humans, free earlobes (E) are dominate to attached earlobes (e) and the presence of freckles (F) is dominate to the absence of freckles (f). If an individual heterozygous for both of these traits were to mate with an individual with attached earlobes and no freckles, what is the probability of having a child with attached earlobes and freckles? |
25% |
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In a DNA double helix, adenine pairs with ___ and guanine pairs with ___. |
Thymine...Cytosine |
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What characteristic is seen in prophase I that does not occur in prophase II? |
Crossing over occurs |
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Hypophosphathemia (vitamin D-resistant rickets) is inherited as a sex-linked dominate trait. The relevant gene is found on the X chromosome. What is the expected outcome of a cross between a homozygous recessive woman and a man with hypophosphatemia? |
All of their daughters and none of their sons exhibit hypophosphatemia |
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The cell cycle results in the production of |
Two cells, each with the same amount of genetic material and the same genetic infomration |
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Sexual intercourse in humans |
Allows a haploid sperm cell to fertilize a haploid egg cell. |
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What is the difference between a benign and a malignant tumor? |
Benign tumors do not metastasize; malignant tumors do. |
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A couple has two female children. What is the probability that their next child will be male? |
50% |
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The expressed (coding) regions of eykaryotic genes are called |
exons |
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RNA contains the nitrogenous base ___ instead of ___, which is only found in DNA. |
Uracil...Thymine |
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What is the key to the recognition of incomplete dominance? |
The phenotype of the heterozygote falls between the phenotypes of the homozygoes. |
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The correct sequence of the events occurring during transcription is |
Initiation, elongation, termination |
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An individual with (naturally) curly hair and an individual with (naturally) straight hair mate; all of their offspring have (naturally) wavy hair. What is the relationship between the alleles for hair texture? |
Incomplete dominance |
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An individual with (naturally) curly hair and an individual with (naturally) straight hair mate; all of their offspring have (naturally) wavy hair.If an individual with wavy hair mates with an individual with straight hair, what is the probability that their child will have curly hair? |
0% |
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A(n) ___ is an example of an organism that can sometimes reproduce asexually by parthenogensis. |
Komodo dragon |
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Linked genes are usually |
Located close together on a chromosome |
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Achondroplasia is a form of dwarfism caused by a dominate allele. The homozygous dominant genotype causes death, so individuals who have this condition are all heterozygotes. If a person with achondroplasia mates with a person who does not have achondroplasia, what percentage of their children would be expected to have achondroplasia? |
50% |