Genetics and Evolution Exam - Test 1

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Questions and Answers

Genes exist in alternative forms called alleles.

True (A)

If a person with Huntington's disease (heterozygous) mates with a normal person, what are the chances (percentage) of them having a child with the disease?

  • 50 (correct)
  • 75
  • 0
  • 100

Trisomy 18 is also known as __________ syndrome.

Patau's

How many pairs of chromosomes do human beings have?

<p>23 pairs</p> Signup and view all the answers

Nondisjunction happens only in sex chromosomes.

<p>False (B)</p> Signup and view all the answers

Match the chromosomal condition with its description:

<p>Turner's syndrome = 45X genomic compliment Trisomy 21 = Down syndrome Klinefelter's syndrome = 47XXY condition Trisomy 18 = Patau's syndrome</p> Signup and view all the answers

In humans, the X chromosome is larger than the Y chromosome.

<p>True (A)</p> Signup and view all the answers

If two individuals with brachydactyly (both heterozygous) have children, what percentage of their children would typically exhibit brachydactyly?

<p>75 (B)</p> Signup and view all the answers

Humans have _____ pairs of chromosomes.

<p>23 (C)</p> Signup and view all the answers

Germ cells do not go through mitosis.

<p>True (A)</p> Signup and view all the answers

What is the end product of meiosis called?

<p>Gametes</p> Signup and view all the answers

A _____ cross is when two individuals with different traits are bred.

<p>hybrid</p> Signup and view all the answers

Which statement is false?

<p>Karyotypes contain the same number of chromosomes in all species. (D)</p> Signup and view all the answers

A homozygous dominant individual and a heterozygous individual will likely have a child with sickle cell disease.

<p>False (B)</p> Signup and view all the answers

Match the following chromosomal terms with their descriptions:

<p>Chromosomal Abnormalities = Changes in chromosome structure or number Meiosis = Process that reduces chromosome number by half Gametes = Haploid reproductive cells Gene Expression = Process by which information from a gene is used to synthesize a functional gene product</p> Signup and view all the answers

What is the unit for distance on a chromosome?

<p>mu (map units)</p> Signup and view all the answers

What would be the chances of having an affected child if two heterozygous for Tay-Sachs disease mate?

<p>25 (D)</p> Signup and view all the answers

If an albino individual mates with a normal homozygous individual, what percentage of their offspring would likely be albinos?

<p>0 (B)</p> Signup and view all the answers

Edwards syndrome would be described as:

<p>2n+1 (C)</p> Signup and view all the answers

A-DNA is the normal DNA found in cells.

<p>False (B)</p> Signup and view all the answers

Crossing over in prophase 1 occurs between the X and Y chromosomes.

<p>False (B)</p> Signup and view all the answers

What term refers to the position of a gene on a chromosome?

<p>locus</p> Signup and view all the answers

The gene responsible for color blindness is located on the ______ chromosome.

<p>X</p> Signup and view all the answers

Match the following concepts with their definitions:

<p>Gene expression = The process by which information from a gene is used to synthesize a functional gene product Transcription = The process of copying a segment of DNA into RNA Meiosis = A type of cell division that reduces the number of chromosomes in gametes Chromosomal abnormality = A structural or numerical alteration of chromosomes</p> Signup and view all the answers

Flashcards

Alleles

Alternative forms of a gene.

Human Chromosomes

Human beings have 46 chromosomes, not pairs.

Nondisjunction

Failure of chromosomes to separate properly during cell division.

Patau's Syndrome

Trisomy 13 (not 18).

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Trisomy

An organism with an extra chromosome.

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Sex Determination (Humans)

Females have XX chromosomes and Males XY chromosomes.

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Meiosis Gametes

The end product of meiosis are gametes (sex cells) used for sexual reproduction.

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Huntington's Disease Heterozygote

50% chance of offspring inheriting the disease if one parent has Huntington's disease and the other is normal.

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Tay-Sachs Disease Inheritance

Two heterozygous parents for Tay-Sachs disease have a 25% chance of having an affected child.

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Albinism Inheritance

An albino individual mating with a normal homozygous individual will have 0% chance of having albino offspring.

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Edwards Syndrome

Edwards syndrome is a chromosomal disorder characterized by trisomy 18 (2n+1).

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A-DNA

A-DNA is not the normal DNA found in cells. The normal form is B-DNA.

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Gene Linkage

Genes responsible for color blindness and hemophilia are located on the X chromosome and are linked, meaning they are inherited together.

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Transformation

Transformation can be used to determine gene linkage, gene order, and map distance.

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Locus

The locus refers to the specific position of a gene on a chromosome.

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Bacterial Conjugation

Bacterial conjugation is an example of horizontal gene transfer, where genetic material is transferred between bacteria.

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Diploid Number

The normal number of chromosomes in a cell, usually two sets (one from each parent).

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Syngamy

The fusion of two gametes (sex cells) to form a zygote, restoring the diploid number of chromosomes.

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True Breeding

Individuals that only produce offspring with the same trait, meaning they have two identical alleles for that trait.

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Genomics

The study of genes, their structure, function, and inheritance patterns within a population.

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Meiosis I

The first stage of meiosis, where homologous chromosomes pair up and exchange genetic material, resulting in two daughter cells with half the number of chromosomes.

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Dihybrid Cross

A cross between individuals that differ in two traits, for example, flower color and seed shape.

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Reciprocal Cross

A cross where the traits of the parents are reversed, for example, switching the male and female parent.

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Dominant Trait

A trait that masks the expression of another trait, even if only one copy of the dominant allele is present.

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Study Notes

Genetics and Evolution Exam - Test 1

  • Genes exist in alternative forms called alleles. (True or False)
  • Humans have 46 chromosomes, not pairs. (False)
  • Nondisjunction only occurs in sex chromosomes. (False)
  • Patau's syndrome is also known as trisomy 18. (True)
  • Triploidy refers to an organism with four sets of chromosomes. (True)
  • Chromosomes carry genes, not the other way around. (False)
  • A male has 22 pairs of homologous chromosomes and 2 non-homologous sex chromosomes (XY). (True)
  • A female's sex is determined by the absence of the Y chromosome. (True)
  • Environmental factors can influence sex determination. (True or False)
  • Meiosis produces gametes. (True or False)
  • Primary nondisjunction occurs during meiosis, secondary during mitosis. (False)
  • A pink flower from a cross of red and white is an example of codominance. (True or False)
  • A test cross in corn showing only tall plants indicates a homozygous dominant genotype. (True or False)
  • Sickle cell anemia is a sex-linked trait. (True or False)
  • Trisomy means an extra chromosome. (True or False)
  • In birds/butterflies, hemizygosity occurs only in males. (True or False)
  • Turner syndrome has 45 chromosomes (45X) in humans. (True or False)
  • Dioecious plants have male and female organs on the same plant. (True or False)
  • The X chromosome is larger than the Y in humans. (True or False)
  • Trisomy X is a sex-chromosome disorder, not an autosomal one. (True or False)

Genetics and Evolution Exam - Test 2

  • Multiple Choice: Huntington's disease (heterozygous) child chance : 50%
  • Multiple Choice: Brachydactyly (heterozygous) mating: 75% chance brachydactyl child
  • Multiple Choice: Tay-Sachs (heterozygous mating): 25% chance affected child
  • Multiple Choice: Albinism (heterozygous): 50% chance albino child
  • Multiple Choice: Edwards Syndrome: 2n - 1

Genetics Test 2

  • A-DNA is the standard DNA in cells. (True or False)
  • Crossing over, during prophase I, doesn’t happen between X and Y. (True or False)
  • Color blindness and hemophilia genes are linked. (True or False)
  • Transformation can determine gene linkage, gene order and map distance. (True or False)
  • A gene's location on a chromosome is the locus. (True or False)
  • Bacterial conjugation is a vertical gene transfer example. (False)
  • A gene coding for mRNA is called a protein-coding gene. (True or False)
    • DNA polymerase polymerizes DNA, not primase. (False)
  • tRNA brings amino acids to the ribosome A site. (True)
  • The nitrogen base attaches to the 1' carbon. (True or False)
  • Karyotyping detects chromosomal mutations. (True or False)
  • The transcribed segment is a gene. (True or False)
  • mRNA production occurs from a coding, not a template strand. (False)
  • Transcription is directional (5' → 3') (True or False)
  • Phages can be genetic material transfer vectors. (True or False)
  • Nucleotides bond via phosphodiester bridges). (True or False)
  • mRNA is read in three-base codon units. (True or False)
  • Eukaryotes have introns. Transcription doesn't always finish before translation begins. (True or False)
  • Multiple Choice: RNA bases: adenine, guanine, cytosine, uracil
  • Multiple Choice: Transcription Enzyme: RNA polymerase
  • Multiple Choice: Exon joining process: RNA splicing
  • Multiple Choice: Transcription location in eukaryotes: nucleus
  • Multiple Choice: Genetic Code location: mRNA
  • Multiple Choice: Non-DNA Replication Enzyme: primase (or RNA primase)

Other Questions/Tests

  • Additional questions cover a range of topics, including the sequences of specific genetic processes, the roles of various molecules in these processes, and the calculation of probabilities related to genetic traits. These notes cover gene location on chromosomes, different types of mutations, and other related genetic concepts.

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