Genetics and Heredity

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Questions and Answers

Which type of mutation involves the addition of a nucleotide, leading to a shift in the reading frame and alteration of the amino acid sequence after the insertion point?

  • Point mutation
  • Substitution mutation
  • Deletion mutation
  • Insertion mutation (correct)

A mutation in a non-coding region of DNA does not alter the amino acid sequence. What is the likely effect of this mutation?

  • It will always result in a catastrophic disease.
  • It will always result in a genetic advantage.
  • It may have no observable effect on the phenotype. (correct)
  • It will always affect transcription and translation.

In a monohybrid cross, if both parents are heterozygous for a particular trait (Aa), what is the probability of their offspring being homozygous recessive (aa)?

  • 75%
  • 25% (correct)
  • 100%
  • 50%

A plant breeder has a plant with a dominant phenotype but an unknown genotype. Which type of cross should the breeder perform to determine the genotype of this plant?

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

In humans, blood type AB is an example of codominance. If a person with blood type A has offspring with a person with blood type B, what are the possible blood types of their offspring?

<p>A, B, AB, or O (A)</p> Signup and view all the answers

In a pedigree diagram, what does a shaded circle typically represent?

<p>An affected female (D)</p> Signup and view all the answers

Why are recessive sex-linked traits more commonly expressed in males than in females?

<p>Males only have one X chromosome. (D)</p> Signup and view all the answers

In cystic fibrosis, the CFTR protein is non-functional. What is the direct consequence of its malfunction in the respiratory system?

<p>Thick, sticky mucus (B)</p> Signup and view all the answers

How does cystic fibrosis affect the digestive system, specifically concerning the pancreas?

<p>Enzyme build-up and potential digestion of pancreatic tissue (D)</p> Signup and view all the answers

What is the purpose of pre-implantation genetic diagnosis (PGD) in genetic screening?

<p>To screen for genetic abnormalities in embryos created through in vitro fertilization before implantation. (C)</p> Signup and view all the answers

Flashcards

Gene Mutation

A random, permanent change in DNA that can alter protein production.

Insertion Mutation

Adds a base, shifting the reading frame forward and altering the amino acid sequence.

Deletion Mutation

Removes a base, shifting the reading frame backward and altering subsequent amino acids.

Phenotype

The physical trait expressed, resulting from genotype and environmental interaction.

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Genotype

The genetic makeup of an organism for a particular trait.

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Homozygous

Having identical alleles for a trait.

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Codominance

Occurs when both alleles present are expressed, as seen in human AB blood types.

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Pedigree Diagram

Shows trait inheritance and offspring probabilities.

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Sex Linkage

Genes carried on the X chromosome.

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Cystic Fibrosis

A genetic condition caused by a mutation in the CFTR gene, leading to thick, sticky mucus.

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Study Notes

All information provided in the text was already present in the existing notes. Therefore, no updates or changes were needed.

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