A diploid human cell that is dividing will contain _______ chromosomes. These chromosomes will each consist of _______ chromatids. Fill in the corresponding blanks.

Human chromosomes are divided into two arms, a long q arm and a short p arm.  A karyotype is the organization of a human cell’s total genetic complement.  A typical karyotype is generated by ordering chromosome 1 to chromosome 23 in order of decreasing size. 

When viewing a karyotype, it can often become apparent that changes in chromosome number, arrangement, or structure are present.  Among the most common genetic changes are Robertsonian translocations, involving transposition of chromosomal material between long arms of certain chromosomes to form one derivative chromosome.  Chromosomes 14 and 21, for example, often undergo a Robertsonian translocation, as below.

A karyotype of this individual for chromosomes 14 and 21 would thus appear as follows:

Though an individual with aberrations such as a Robertsonian translocation may be phenotypically normal, they can generate gametes through meiosis that have atypical organizations of chromosomes, resulting in recurrent fetal abnormalities or miscarriages.

In a normal chromosome 14, what region of the chromosome exists between the p arm and the q arm?

The concept of genomic imprinting is important in human genetics. In genomic imprinting, a certain region of DNA is only expressed by one of the two chromosomes that make up a typical homologous pair. In healthy individuals, genomic imprinting results in the silencing of genes in a certain section of the maternal chromosome 15. The DNA in this part of the chromosome is "turned off" by the addition of methyl groups to the DNA molecule. Healthy people will thus only have expression of this section of chromosome 15 from paternally-derived DNA.

The two classic human diseases that illustrate defects in genomic imprinting are Prader-Willi and Angelman Syndromes. In Prader-Willi Syndrome, the section of paternal chromosome 15 that is usually expressed is disrupted, such as by a chromosomal deletion. In Angelman Syndrome, maternal genes in this section are deleted, while paternal genes are silenced. Prader-Willi Syndrome is thus closely linked to paternal inheritance, while Angelman Syndrome is linked to maternal inheritance.

Figure 1 shows the chromosome 15 homologous pair for a child with Prader-Willi Syndrome. The parental chromosomes are also shown. The genes on the mother’s chromosomes are silenced normally, as represented by the black boxes. At once, there is also a chromosomal deletion on one of the paternal chromosomes. The result is that the child does not have any genes expressed that are normally found on that region of this chromosome.

Imagine the child in figure 1 was diagnosed at birth with cystic fibrosis as well as Prader-Willi. Cystic fibrosis is due to a recessive genetic mutation on chromosome 7. Two years later, his parents have another child that has cystic fibrosis, but not Prader-Willi. Which of the following best explains why Prader-Willi and cystic fibrosis are not always inherited together ?

The concept of genomic imprinting is important in human genetics. In genomic imprinting, a certain region of DNA is only expressed by one of the two chromosomes that make up a typical homologous pair. In healthy individuals, genomic imprinting results in the silencing of genes in a certain section of the maternal chromosome 15. The DNA in this part of the chromosome is "turned off" by the addition of methyl groups to the DNA molecule. Healthy people will thus only have expression of this section of chromosome 15 from paternally-derived DNA.

The two classic human diseases that illustrate defects in genomic imprinting are Prader-Willi and Angelman Syndromes. In Prader-Willi Syndrome, the section of paternal chromosome 15 that is usually expressed is disrupted, such as by a chromosomal deletion. In Angelman Syndrome, maternal genes in this section are deleted, while paternal genes are silenced. Prader-Willi Syndrome is thus closely linked to paternal inheritance, while Angelman Syndrome is linked to maternal inheritance.

Figure 1 shows the chromosome 15 homologous pair for a child with Prader-Willi Syndrome. The parental chromosomes are also shown. The genes on the mother’s chromosomes are silenced normally, as represented by the black boxes. At once, there is also a chromosomal deletion on one of the paternal chromosomes. The result is that the child does not have any genes expressed that are normally found on that region of this chromosome.

Based on the information in the passage, which of the following is true of Prader-Willi Syndrome?

I. It must involve a chromosomal deletion on the paternal chromosome 15

II. It must involve normal silencing of maternal chromosome 15

III. It is a sex-linked disorder because it involves chromosome 15

The concept of genomic imprinting is important in human genetics. In genomic imprinting, a certain region of DNA is only expressed by one of the two chromosomes that make up a typical homologous pair. In healthy individuals, genomic imprinting results in the silencing of genes in a certain section of the maternal chromosome 15. The DNA in this part of the chromosome is "turned off" by the addition of methyl groups to the DNA molecule. Healthy people will thus only have expression of this section of chromosome 15 from paternally-derived DNA.

The two classic human diseases that illustrate defects in genomic imprinting are Prader-Willi and Angelman Syndromes. In Prader-Willi Syndrome, the section of paternal chromosome 15 that is usually expressed is disrupted, such as by a chromosomal deletion. In Angelman Syndrome, maternal genes in this section are deleted, while paternal genes are silenced. Prader-Willi Syndrome is thus closely linked to paternal inheritance, while Angelman Syndrome is linked to maternal inheritance.

Figure 1 shows the chromosome 15 homologous pair for a child with Prader-Willi Syndrome. The parental chromosomes are also shown. The genes on the mother’s chromosomes are silenced normally, as represented by the black boxes. At once, there is also a chromosomal deletion on one of the paternal chromosomes. The result is that the child does not have any genes expressed that are normally found on that region of this chromosome.

Chromosome 15 is an autosome. Which of the following is (are) true of all autosomes?

I. They contain histones

II. They determine chromosomal sex

III. They align on the metaphase plate during mitosis

Human chromosomes are divided into two arms, a long q arm and a short p arm.  A karyotype is the organization of a human cell’s total genetic complement.  A typical karyotype is generated by ordering chromosome 1 to chromosome 23 in order of decreasing size. 

When viewing a karyotype, it can often become apparent that changes in chromosome number, arrangement, or structure are present.  Among the most common genetic changes are Robertsonian translocations, involving transposition of chromosomal material between long arms of certain chromosomes to form one derivative chromosome.  Chromosomes 14 and 21, for example, often undergo a Robertsonian translocation, as below.

A karyotype of this individual for chromosomes 14 and 21 would thus appear as follows:

Though an individual with aberrations such as a Robertsonian translocation may be phenotypically normal, they can generate gametes through meiosis that have atypical organizations of chromosomes, resulting in recurrent fetal abnormalities or miscarriages.

In der(14,21), which region of a chromosome might you expect to find in the center of its structure?

A man with type AB blood marries a woman with type A blood. Which of the following blood types might their sons inherit?