Non-Mendelian  Inheritance (Hard)
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Non-Mendelian Inheritance (Hard)

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Questions and Answers

What is the function of the imprinting control region (ICR) in genomic imprinting?

  • To activate transcription of the imprinted gene
  • To bind transcription factors that regulate the imprinted gene (correct)
  • To methylate the imprinted gene in both oocyte and sperm
  • To demethylate the imprinted gene
  • What happens to methylation in gamete-forming cells?

  • Methylation is replaced by histone modification
  • Methylation is removed (correct)
  • Methylation is maintained
  • Methylation is inherited from the parent
  • What is the result of methylation on gene transcription?

  • Inhibition of transcription (correct)
  • No effect on transcription
  • Variable effect on transcription
  • Activation of transcription
  • What is the unit of genomic imprinting?

    <p>All of the above</p> Signup and view all the answers

    What is the purpose of genomic imprinting in some species?

    <p>X inactivation</p> Signup and view all the answers

    In which cells is the pattern of methylation maintained?

    <p>Somatic cells</p> Signup and view all the answers

    What is the main purpose of dosage compensation?

    <p>To offset differences in the number of active sex chromosomes</p> Signup and view all the answers

    What is a characteristic of epigenetic inheritance?

    <p>It is caused by chromosomal modifications</p> Signup and view all the answers

    During which stages of development can epigenetic changes occur?

    <p>During oogenesis, spermatogenesis, or early embryonic development</p> Signup and view all the answers

    What is the mechanism of dosage compensation in placental mammals?

    <p>One of the X chromosomes in females is inactivated</p> Signup and view all the answers

    What is an example of a species where the X chromosome from the male parent is inactivated?

    <p>Certain species, but not humans</p> Signup and view all the answers

    Why does dosage compensation occur?

    <p>To offset differences in the number of active sex chromosomes</p> Signup and view all the answers

    What type of modifications can cause epigenetic changes?

    <p>Chromosomal and DNA modifications</p> Signup and view all the answers

    What is the significance of epigenetic inheritance?

    <p>It does not change the DNA sequence, but alters gene expression</p> Signup and view all the answers

    What is the primary function of the Xic during X-chromosome inactivation?

    <p>To maintain the inactivated X chromosome during subsequent cell divisions</p> Signup and view all the answers

    Which of the following statements about genomic imprinting is TRUE?

    <p>It is a mechanism that ensures monoallelic expression of imprinted genes</p> Signup and view all the answers

    What is the effect of the Igf2− allele on the size of a mouse?

    <p>It causes the mouse to be smaller in size, but only if inherited from the female parent</p> Signup and view all the answers

    What is the percentage of X-linked genes in humans that may escape full inactivation?

    <p>Up to 25%</p> Signup and view all the answers

    Which of the following genes is an example of genomic imprinting in the mouse?

    <p>Igf2</p> Signup and view all the answers

    What is the term used to describe the phenomenon of genes being expressed from only one parent?

    <p>Monoallelic expression</p> Signup and view all the answers

    What is the mechanism thought to be involved in the escape of X-linked genes from inactivation?

    <p>Loosening of chromatin in specific regions</p> Signup and view all the answers

    Which of the following is a characteristic of genomic imprinting?

    <p>It is a heritable epigenetic phenomenon</p> Signup and view all the answers

    Study Notes

    Epigenetic Inheritance

    • Epigenetic inheritance refers to a pattern in which a modification occurs to a nuclear gene or chromosome, altering gene expression, but the DNA sequence remains unchanged.
    • Epigenetic changes are caused by DNA and chromosomal modifications that can occur during oogenesis, spermatogenesis, or early embryonic development.

    Dosage Compensation

    • Dosage compensation offsets differences in the number of active sex chromosomes.
    • It has been studied in mammals, Drosophila, and Caenorhabditis elegans, with different mechanisms depending on the species.
    • In placental mammals, one of the X chromosomes in somatic cells of females is inactivated, or the X chromosome from the male parent is inactivated, or either of the two X chromosomes is randomly inactivated.

    Genomic Imprinting

    • Genomic imprinting occurs in several species, including insects, mammals, and flowering plants, involving a single gene, part of a chromosome, an entire chromosome, or all chromosomes from one parent.
    • It can be used for X inactivation in some species.
    • Imprinting involves a marking process, with an imprinting control region (ICR) located near the imprinted gene, which is methylated either in the oocyte or sperm, but not both.
    • For most genes, methylation causes inhibition of transcription.

    Pattern of Methylation and X-Chromosome Inactivation

    • Each parent inherits one methylated and one unmethylated gene, which is maintained in somatic cells, and methylation is removed in gamete-forming cells.
    • The inactivated X chromosomes is maintained as such during subsequent cell divisions.
    • Some genes on the inactivated X chromosome are expressed in somatic cells of adult female mammals, including pseudoautosomal genes, which do not require dosage compensation.

    Genomic Imprinting and Gene Expression

    • Genomic imprinting results in the expression of either the maternally-inherited or the paternally-inherited allele, but not both, a phenomenon known as monoallelic expression.
    • The Igf2 gene in mice is an example of genomic imprinting, where the paternal allele is transcribed into RNA, but the maternal allele is not.

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    Explore epigenetic inheritance and dosage compensation, concepts crucial to understanding gene expression and chromosomal development.

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