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Indicate the expected number of Barr bodies in interphase cells of individuals with (a) triple \(X\) syndrome \((X X X)\) (b) \(\mathrm{XYY}\) syndrome, (c) Klinefelter syndrome, (d) Turner syndrome, and karyotype \(48, \mathrm{XXXX}\)

Short Answer

Expert verified
Answer: Triple X Syndrome - 2 Barr bodies; XYY Syndrome - 0 Barr bodies; Klinefelter Syndrome - 1 Barr body; Turner Syndrome - 0 Barr bodies; Karyotype 48, XXXX - 3 Barr bodies.

Step by step solution

01

Triple X Syndrome (XXX)

For individuals with Triple X Syndrome, they possess three X chromosomes (XXX). Using the formula, we can find the number of Barr bodies: Number of Barr bodies = (Total X chromosomes - 1) = (3 - 1) = 2 Thus, individuals with Triple X Syndrome have 2 Barr bodies in their interphase cells.
02

XYY Syndrome

For individuals with XYY Syndrome, they possess one X chromosome and two Y chromosomes (XYY). Using the formula, we can find the number of Barr bodies: Number of Barr bodies = (Total X chromosomes - 1) = (1 - 1) = 0 Thus, individuals with XYY Syndrome have 0 Barr bodies in their interphase cells.
03

Klinefelter Syndrome

For individuals with Klinefelter Syndrome, they possess two X chromosomes and one Y chromosome (XXY). Using the formula, we can find the number of Barr bodies: Number of Barr bodies = (Total X chromosomes - 1) = (2 - 1) = 1 Thus, individuals with Klinefelter Syndrome have 1 Barr body in their interphase cells.
04

Turner Syndrome

For individuals with Turner Syndrome, they possess one X chromosome only (X). Using the formula, we can find the number of Barr bodies: Number of Barr bodies = (Total X chromosomes - 1) = (1 - 1) = 0 Thus, individuals with Turner Syndrome have 0 Barr bodies in their interphase cells.
05

Karyotype 48, XXXX

For individuals with karyotype 48, XXXX, they possess four X chromosomes (XXXX). Using the formula, we can find the number of Barr bodies: Number of Barr bodies = (Total X chromosomes - 1) = (4 - 1) = 3 Thus, individuals with karyotype 48, XXXX have 3 Barr bodies in their interphase cells.

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Most popular questions from this chapter

Distinguish between the concepts of sex determination and sexual differentiation.

An attached-X female fly, XXY (see the Insights and Solutions box), expresses the recessive X-linked white-eye phenotype. It is crossed to a male fly that expresses the X-linked recessive miniature wing phenotype. Determine the outcome of this cross in terms of sex, eye color, and wing size of the offspring.

An insect species is discovered in which the heterogametic sex is unknown. An X-linked recessive mutation for reduced wing (rw) is discovered. Contrast the \(F_{1}\) and \(F_{2}\) generations from a cross between a female with reduced wings and a male with normalsized wings when (a) the female is the heterogametic sex. (b) the male is the heterogametic sex.

The genes encoding the red-and green-color-detecting proteins of the human eye are located next to one another on the X chromosome and probably evolved from a common ancestral pigment gene. The two proteins demonstrate 76 percent homology in their amino acid sequences. A normal-visioned woman with both genes on each of her two X chromosomes has a redcolor-blind son who was shown to have one copy of the greendetecting gene and no copies of the red-detecting gene. Devise an explanation for these observations at the chromosomal level (involving meiosis).

It is believed that any male-determining genes contained on the Y chromosome in humans are not located in the limited region that synapses with the X chromosome during meiosis. What might be the outcome if such genes were located in this region?

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