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What are inversion heterozygotes? How can meiotic pairing occur in these organisms? What will be the consequence?

Short Answer

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Answer: Inversion heterozygotes are individuals with one normal and one inverted chromosome, which they inherited from a parent with a chromosome inversion. Meiotic pairing occurs in these organisms through the formation of an inversion loop, allowing the chromosomes to align and recombine properly. However, this process can lead to the production of abnormal gametes, lower recombination rates, and reduced fertility.

Step by step solution

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1. Chromosome Inversions

Chromosome inversions occur when a section of a chromosome breaks off, flips around and reattaches itself to the same chromosome. This results in the affected region being present in reverse order compared to the normal orientation. There are two types of inversions: paracentric (doesn't include centromere) and pericentric (includes centromere).
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2. Inversion Heterozygotes

Inversion heterozygotes have one chromosome with the normal orientation of the DNA sequence and the other chromosome with an inverted DNA sequence. These individuals are heterozygous for the inversion, as they have one normal and one inverted chromosome.
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3. Meiotic Pairing in Inversion Heterozygotes

During meiosis, homologous chromosomes need to pair with each other to allow recombination and exchange genetic information. In inversion heterozygotes, pairing can occur between the normal and inverted chromosomes by forming a loop-like structure where the two chromosomes align in the inverted regions. This process is known as the formation of an inversion loop, which allows the chromosomes to align and recombine properly.
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4. Consequences of Meiotic Pairing in Inversion Heterozygotes

Although inversion loops help create correct chromosome alignment during meiosis, mistakes in repair or recombination can lead to the production of abnormal gametes. These gametes may have chromosome duplications or deletions, which can cause serious consequences for the offspring if fertilization occurs. Additionally, inversion heterozygotes may have lower fertility rates as a result of lowered recombination rates, especially if the inversion is large and affects many genes. In summary, inversion heterozygotes are individuals with one normal and one inverted chromosome, which they inherited from a parent with a chromosome inversion. Meiotic pairing can occur in these organisms through the formation of an inversion loop. The consequence of meiotic pairing in inversion heterozygotes can include the production of abnormal gametes, lower recombination rates, and reduced fertility.

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Most popular questions from this chapter

A couple planning their family are aware that through the past three generations on the husband's side a substantial number of stillbirths have occurred and several malformed babies were born who died early in childhood. The wife has studied genetics and urges her husband to visit a genetic counseling clinic, where a complete karyotype-banding analysis is performed. Although the tests show that he has a normal complement of 46 chromosomes, banding analysis reveals that one member of the chromosome 1 pair (in group \(A\) ) contains an inversion covering 70 percent of its length. The homolog of chromosome 1 and all other chromosomes show the normal banding sequence. (a) How would you explain the high incidence of past stillbirths? (b) What can you predict about the probability of abnormal- ity/normality of their future children? (c) Would you advise the woman that she will have to bring each pregnancy to term to determine whether the fetus is normal? If not, what else can you suggest?

What are the possible reasons behind translocations?

What evidence indicates that humans with aneuploid karyotypes occur at conception but are usually inviable?

In this chapter, we have focused on chromosomal mutations resulting from a change in number or arrangement of chromosomes. In our discussions, we found many opportunities to consider the methods and reasoning by which much of this information was acquired. From the explanations given in the chapter, what answers would you propose to the following fundamental questions? (a) How do we know that the extra chromosome causing Down syndrome is usually maternal in origin? (b) How do we know that human ancuploidy for each of the 22 autosomes occurs at conception, even though most often human aneuploids do not survive embryonic or fetal development and thus are never observed at birth? (c) How do we know that specific mutant phenotypes are due to changes in chromosome number or structure? (d) How do we know that the mutant Bar-eye phenotype in Drosophila is due to a duplicated gene region rather than to a change in the nucleotide sequence of a gene?

Contrast the genetic composition of gametes derived from tetrads of inversion heterozygotes where crossing over occurs within a paracentric versus a pericentric inversion.

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