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If the inheritance of two traits fully obeys Mendelian laws of inheritance, where may you assume that the genes are located? a. on any autosomal chromosome or chromosomes b. on Y chromosomes c. on the same chromosome d. on separate chromosomes

Short Answer

Expert verified
d. on separate chromosomes

Step by step solution

01

Understand Mendelian Inheritance

Mendelian inheritance refers to the patterns that govern how traits are passed from parents to offspring, based on Gregor Mendel's principles. This includes the concepts of dominant and recessive alleles, as well as the law of segregation and the law of independent assortment.
02

Law of Independent Assortment

According to the law of independent assortment, genes for different traits can segregate independently during the formation of gametes. This typically occurs when the genes are located on different chromosomes or are far apart on the same chromosome.
03

Analyze the Options

a. Any autosomal chromosome(s) implies the genes can be on any non-sex chromosome. b. Genes on Y chromosomes would not follow independent assortment unless they are the only traits considered. c. Genes on the same chromosome are unlikely unless they are far apart, allowing for crossing over to occur. d. On separate chromosomes aligns with the law of independent assortment best.
04

Choose the Best Answer

Given that fully Mendelian inheritance requires independent assortment of the traits, the most likely location of the genes is on separate chromosomes.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Law of Independent Assortment
The law of independent assortment is one of the fundamental principles of Mendelian inheritance. It states that genes for different traits can segregate, or separate, independently during the formation of gametes. This means that the inheritance of one trait is not affected by the inheritance of another.
For example, if you're considering traits like seed color and seed shape in pea plants, the gene for seed color will segregate independently from the gene for seed shape. This typically happens when the genes are on different chromosomes or when they are positioned far apart on the same chromosome, allowing for recombination.
This principle helps explain the genetic variation observed in offspring.
Dominant and Recessive Alleles
Understanding dominant and recessive alleles is crucial when studying Mendelian inheritance. Alleles are different forms of a gene. When an individual has two different alleles for a trait, the dominant allele will mask the expression of the recessive allele.
For example, if the allele for yellow seeds (Y) is dominant over the allele for green seeds (y), a plant with the genotype Yy will have yellow seeds.
  • Dominant alleles: Represented by a capital letter (e.g., Y)
  • Recessive alleles: Represented by a lowercase letter (e.g., y)
Only if an individual has two recessive alleles (yy) will the recessive trait be expressed. This predictable pattern helps us to determine the possible genetic outcomes in offspring.
Segregation of Genes
The law of segregation is another key concept in Mendelian genetics. It states that during the formation of gametes (sperm or eggs), the two alleles for a trait separate so that each gamete carries only one allele for each gene.
This ensures that offspring receive one allele from each parent. For instance, if a parent has a genotype Aa, the gametes will carry either the A allele or the a allele, but not both. This segregation occurs during meiosis, a special type of cell division that halves the number of chromosomes.
This law is fundamental to understanding how traits are inherited and reinforces why offspring have a combination of traits from both parents.

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Most popular questions from this chapter

Which cellular process underlies Mendel’s law of independent assortment? a. Chromosomes align randomly during meiosis. b. Chromosomes can exchange genetic material during crossover. c. Gametes contain half the number of chromosomes of somatic cells. d. Daughter cells are genetically identical to parentcells after mitosis.

The trait for widow’s peak can be considered a monoallelic dominant trait in humans. If a man with a widow’s peak and a woman with a straight hairline have a child together, what is the probability that the child will inherit the widow’s peak if you know that the father’s mother had a straight hairline? a. 0.25 b. 0.5 c. 0.75 d. 1

Fruit flies (Drosophila melanogaster) with a wild-type phenotype have gray bodies and red eyes. Certain mutations can cause changes to these traits. Mutant flies may have a black body and/or cinnabar eyes. To study the genetics of these traits, a researcher crossed a truebreeding wild-typed male fly with a true-breeding female fly with a black body and cinnabar eyes. All of the F1 progeny displayed a wild type phenotype. Which of the following is correct about the traits observed? a. Gray body and cinnabar eyes are dominant. b. Eye color is sex-linked. c. Body color is sex-linked. d. Gray body and red eyes are dominant.

Flower position in pea plants is determined by a gene with axial and terminal alleles. Given that axial is dominant to terminal, list all of the possible F1 and F2 genotypes and phenotypes from a cross involving parents that are homozygous for each trait. Express genotypes with conventional genetic abbreviations. a. F1: All AA-axial; F2: AA-Axial and aa-terminal. b. F1: All aa-terminal; F2: AA-Axial and Aaterminal. c. F1: AA-axial and Aa-terminal; F2: All AA-axial. d. F1: All Aa-axial; F2: AA-Axial, Aa-Axial, and aa-terminal.

Two genes, A and B, are located adjacent to each other (linked) on the same chromosome. In the original cross (P0), one parent is homozygous dominant for both traits (AB), whereas the other parent is recessive (ab). A. Describe the distribution of genotypes and phenotypes in F1. B. Describe the distribution of genotypes and phenotypes when F1 is crossed with the ab parent. C. Describe the distribution of genotypes and phenotypes when F1 is crossed with the AB parent. D. Explain the observed non-Mendelian results in terms of the violation of the laws governing Mendelian genetics.

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