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a. A random mutation process in chromosomes
b. An epigenetic phenomenon leading to functional differences between parental genes
c. A process occurring only in haploid organisms
d. A phenomenon causing changes in DNA sequencing
b
a. Xylem and phloem tissues
b. Haploid generation germ cells resulting from meiosis
c. Roots and stems
d. Pollen and ovules
b
a. Angelman Syndrome
b. Androgenetic zygotes
c. Hydatidiform moles
d. Prader-Willi Syndrome
a and d
a. It affects only a few genes in a specific chromosomal region
b. Imprinting causes changes in chromatin structure and gene expression
c. Imprinted genes are randomly dispersed across chromosomes
d. It impacts gene expression equally from both parental chromosomes
b
a. It silences the active allele
b. It disrupts the imprinting process
c. Both parental alleles have identical methylation patterns
d. Loss of methylation can lead to significant phenotypic effects
d
a. It allows for the expression of both parental alleles equally
b. Deleterious mutations can be masked by a normal allele on the homologous chromosome
c. Diploid organisms have higher mutation rates
d. It prevents gene expression variation
b
a. Paternal genome
b. Maternal genome
c. Both genomes demethylate simultaneously
d. None of the above
a
a. 10-20 genes
b. 50 genes
c. Over 200 genes
d. Less than 5 genes
b
a. Mammals
b. Insects
c. Plants
d. Birds
d
a. Heterochromatinization
b. Endosperm pigment synthesis
c. DNA demethylation
d. Somatic cell division
a
a. Differential gene expression between parental alleles
b. Chromosomal translocation
c. Random mutation occurrence
d. Chromatin rearrangement
a
a. Paternal DNA replication
b. Elimination of DNA methylation
c. Methylation of imprinted genes
d. Chromosomal recombination
c
a. Deficiencies in gene expression from the paternal chromosome region
b. Overexpression of genes on chromosome 15q11-13
c. Abnormal methylation in the imprinted region
d. Loss of DNA methylation
a
a. Activation of gene expression
b. Chromatin compaction
c. Inhibition of gene transcription
d. Enhanced replication rates
c
a. Active alleles replicate earlier than inactive ones
b. Inactive alleles replicate before active ones
c. DNA replication timing remains the same for all alleles
d. Replication timing varies randomly
a
a. Compact chromatin structure
b. Hypersensitivity to nuclease digestion
c. Late replication timing
d. Replication inhibition
b
a. They form ovarian teratomas
b. They show excessive placental growth
c. The embryos die with excessive placental growth
d. They develop without any abnormalities
a
a. Ensuring equal gene expression from parental regions
b. Creating functional differences between paternal and maternal genes
c. Preventing functional differences in offspring
d. Stabilizing chromosomal inheritance
b
a. Pathological states
b. De novo methylation
c. Somatic cell pairing
d. Duplication of parental chromosomes
c
a. It preserves gene patterns between maternal and paternal alleles
b. It disrupts gene expression during embryonic development
c. It ensures proper replication timing
d. It leads to a loss of DNA methylation
a
a. It leads to the preferential inactivation of the maternal X chromosome
b. It causes the loss of maternally derived chromosomes
c. It results in the heterochromatinization and loss of paternally derived chromosomes
d. It triggers abnormal growth patterns in embryonic tissues
c
a. Maternal chromosome set loss in zygotes
b. Loss of paternal chromosome set in zygotes
c. Expression level variation of eye color gene based on parental inheritance
d. Normal gene expression patterns in both maternal and paternal alleles
c
a. Normal development with no abnormalities
b. Differences in embryonic growth patterns
c. Formation of hydatidiform moles in both cases
d. Balanced placental growth rates
b
a. Hemophilia and Sickle Cell Anemia
b. Prader-Willi Syndrome and Angelman Syndrome
c. Cystic Fibrosis and Huntington's Disease
d. Alzheimer's and Parkinson's Disease
b
a. It leads to preferential inactivation of the maternal X chromosome
b. It causes abnormal growth in embryonic tissues
c. It results in the loss of paternally derived chromosomes
d. It triggers differential gene expression based on parental origin
a
a. Excessive placental growth
b. Poor embryonic differentiation
c. Loss of maternal chromosomes
d. Hydatidiform moles formation
d
a. It remains constant regardless of parental origin
b. It is higher when inherited maternally
c. It is higher when inherited paternally
d. It is completely suppressed in both cases
c
a. Proper embryo development
b. Growth failure leading to embryo death
c. Enhanced seed development
d. Increased endosperm pigment synthesis
b
a. Random dispersion of imprinted genes
b. Differential methylation patterns in active alleles
c. Clustering of imprinted genes in specific chromosomal regions
d. Equal expression of imprinted genes from both parental chromosomes
c
a. It is limited to haploid organisms
b. It primarily occurs in germ cells resulting from meiosis
c. It leads to loss of chromosomes in offspring
d. It involves differential gene expression according to parental origin
d
a. It leads to the loss of paternally derived chromosomes
b. It results in the preferential inactivation of the maternal X chromosome
c. It causes abnormal growth patterns in embryonic tissues
d. It triggers gene expression differences based on parental origin
b
a. Normal development with no abnormalities
b. Differences in placental growth rates
c. Formation of hydatidiform moles in both cases
d. Varied embryonic growth patterns
b