Dosage Compensation & Genomic Imprinting

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Welcome! 9.3 Dosage Compensation & Genomic Imprinting โ€” Test 2 — 20 questions, CSIR-NET style.

What this test covers

  • X-inactivation, XIST & Barr bodies
  • Dosage compensation across species
  • Genomic imprinting & parent-of-origin effects
  • DNA methylation, maintenance & resetting

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9.3 Dosage Compensation & Genomic Imprinting โ€” Test 2
Q1. In mammals, dosage compensation equalises X-linked gene expression between the sexes by:โœ“ Inactivating one X chromosome in each female cell
Q2. The molecular modification most associated with maintaining X-chromosome inactivation is:โœ“ DNA methylation
Q3. Dosage compensation in Drosophila is achieved by:โœ“ Hyperactivating the single X in males
Q4. Dosage compensation (as an equalising mechanism for X-linked genes) is found in:โœ“ Insects and mammals
Q5. The pattern of genomic imprinting is maintained across cell generations by:โœ“ DNA methylation
Q6. A gene that is expressed when inherited from the father but silent when inherited from the mother is an example of:โœ“ Genomic imprinting
Q7. A mouse with two normal Igf2 alleles is normal; with two mutant alleles it is dwarf. The size of a heterozygote depends on which parent contributed the wild-type allele. This is:โœ“ Genomic imprinting
Q8. An important property of epigenetic changes (such as methylation marks) is that they:โœ“ Can be inherited from a cell to its daughter cells
Q9. A mouse gene A is needed for normal growth. The cross Aแตˆแต‰หก A (mutant from father) ร— AA gives all-normal offspring, but the cross Aแตˆแต‰หก A (mutant from mother) ร— AA gives 50% small offspring. This is explained by:โœ“ Maternal imprinting (the maternal allele is silenced)
Q10. Which statement about DNA methylation is FALSE?โœ“ Methylation typically occurs at the 5th carbon of cytosine, forming 5-methylcytosine
Q11. The number of Barr bodies in a cell is related to the number of X chromosomes as:โœ“ Number of X chromosomes minus one
Q12. X-inactivation is initiated by a non-coding RNA called:โœ“ XIST
Q13. Prader-Willi and Angelman syndromes, which involve the same chromosomal region (15q11-q13) but different parental origins, are classic examples of:โœ“ Genomic imprinting
Q14. During mammalian gametogenesis, genomic methylation (imprinting) marks are:โœ“ Erased and then reset according to the sex of the individual
Q15. Maintenance DNA methyltransferase (Dnmt1) preferentially acts on:โœ“ Hemimethylated CpG sites after replication
Q16. The inactive X chromosome in a female somatic cell is an example of:โœ“ Facultative heterochromatin
Q17. In C. elegans, dosage compensation in XX hermaphrodites is achieved by:โœ“ Halving transcription from both X chromosomes
Q18. Random X-inactivation makes female mammals:โœ“ Functional mosaics for X-linked genes
Q19. Imprinted genes are notable because, unlike most genes, they are:โœ“ Expressed from only one parental allele
Q20. Match each phenomenon with its mechanism and select the correct option.โœ“ A-ii, B-iii, C-i, D-iv