Solving Genetics Problem: Y-Linked Recessive Trait Inheritance

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Discussion Overview

The discussion revolves around the inheritance mechanism of a specific trait in genetics, focusing on a pedigree analysis involving Y-linked or X-linked recessive traits. Participants explore the implications of these inheritance patterns on carrier probabilities and offspring traits.

Discussion Character

  • Debate/contested
  • Technical explanation
  • Mathematical reasoning

Main Points Raised

  • One participant initially suggests the trait is Y-linked recessive, but this is challenged based on the observation that only females are affected.
  • Another participant proposes that the trait is likely X-linked recessive, arguing that if it were X-linked dominant, one of the parents would have to express the trait.
  • Participants discuss the probability of individual III-2 being a carrier, with one suggesting a 50% chance based on the X-linked recessive model.
  • There is a proposed probability of 25% for the first child of III-3 and III-4 to inherit the trait, contingent on their genotypes.
  • One participant mentions the use of a Punnett square to visualize inheritance patterns and calculate probabilities, while another questions the necessity of this method.
  • There is a discussion about the definitions of heterozygous and homozygous genotypes in the context of the pedigree.

Areas of Agreement / Disagreement

Participants express disagreement regarding whether the trait is Y-linked or X-linked, with no consensus reached on the correct inheritance mechanism. The probabilities suggested for carrier status and offspring traits are also debated, with varying interpretations of the genetic relationships.

Contextual Notes

Participants reference the need for clarity in defining genotypes and the implications of allele combinations, but some assumptions regarding the pedigree and allele representations remain unresolved.

Who May Find This Useful

Individuals interested in genetics, particularly those studying inheritance patterns and pedigree analysis, may find this discussion relevant.

jena
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My Question:
  • What is the mechanism of inheritance for the trait?
  • Which people in the pedigree are known to be heterozygous for the trait?
  • What is the probability that III-2 is a carrier( heterozygous)?
  • If III-3 and III-4 marry, what is the probability that their first child will have the trait?

Picture

View attachment Doc3.docView attachment Doc3.doc

My Answers:
  • Y-Linked recessive
  • I1, I2, II1, and II2
  • ?
  • ?
Of the answers I have so far are these correct?
Thank You :smile:
 
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Are you using the usual convention that males are represented by squares and females by circles? If so, how would it be Y-linked if only females are affected? If you reconsider part 1, the rest will be easier to answer once you've gotten that part.
 
Opps:blushing:
Wouldn't it be X-linked recessive since it couldn't be x-linked dominant otherwise one of the parents would of had it, right?

Also for these questions:

What is the probability that III-2 is a carrier( heterozygous)?
Answer: 50%

If III-3 and III-4 marry, what is the probability that their first child will have the trait?
Answer: 25%

Do I just need to figure them by making a punnett square based off the parents?

Thank You
 
Last edited:
jena said:
Opps:blushing:
Wouldn't it be X-linked recessive since it couldn't be x-linked dominant otherwise one of the parents would of had it, right?
Correct.

With that information, you also have to go back to your answer for the second part.

Also for these questions:
What is the probability that III-2 is a carrier( heterozygous)?
Answer: 50%
Correct.

If III-3 and III-4 marry, what is the probability that their first child will have the trait?
Answer: 25%
Do I just need to figure them by making a punnett square based off the parents?
Thank You
Yes and yes. I think you're getting the hang of this. :smile:
 
jena said:
My Question:
  • What is the mechanism of inheritance for the trait?


  • After meosis , when male and female gametes are fused , each gamete consists of a single gene. When two gamete fuse , they give genotypes which are combinations of alleles. Depending on the nature of the alleles , the phenotypes are formed. This phenotype when expressed shows the particular trait in the individual.

    [*]Which people in the pedigree are known to be heterozygous for the trait?

    People heterozygous for trait are those whose genotype for that particular trait has two alleles each of different type.


    [*]If III-3 and III-4 marry, what is the probability that their first child will have the trait?

    Draw the punnett table and see for yourself.

    BJ
 
I had a similar question, but what would the punnett square look like? Say A = dominant allele and a = recessive allele, then II1: Aa, II2: Aa (parents of III3) and II3: aa, II4: ? (parents of III4)

Would II4 be homozygous dominant (AA) since none of the children have it?

My question also asks to determine the probability using "the law of probability that relates to the simultaneous occurrence of independent events—the product law". I'm unsure of what this means...
 
Never mind about the punnett square
 

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