1Which human blood group system is a classic example of multiple alleles?
Alleles: Multiple alleles
Easy
A.ABO blood group system
B.MN blood group system
C.Duffy blood group system
D.Rh factor system
Correct Answer: ABO blood group system
Explanation:
The ABO blood group is controlled by three alleles (, , and ), making it the classic textbook example of multiple alleles.
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2Multiple alleles refer to the existence of:
Alleles: Multiple alleles
Easy
A.More than two alleles of a gene in a population
B.Genes located on multiple chromosomes
C.Two alleles of a gene in an individual
D.Alleles that always show codominance
Correct Answer: More than two alleles of a gene in a population
Explanation:
Multiple alleles are three or more alternative forms of a gene present at the same locus in a population, though any individual carries only two.
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3In the four o'clock plant, a cross between red-flowered and white-flowered plants gives pink flowers. This is an example of:
Incomplete Dominance and Codominance
Easy
A.Epistasis
B.Codominance
C.Incomplete dominance
D.Complete dominance
Correct Answer: Incomplete dominance
Explanation:
In incomplete dominance, the heterozygote shows an intermediate phenotype (pink) because neither allele is fully dominant over the other.
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4In codominance, the heterozygote shows:
Incomplete Dominance and Codominance
Easy
A.An intermediate blended phenotype
B.No visible phenotype at all
C.Only the dominant allele's phenotype
D.Both alleles expressed fully and simultaneously
Correct Answer: Both alleles expressed fully and simultaneously
Explanation:
In codominance, both alleles are fully and independently expressed in the heterozygote, as seen in AB blood group where both A and B antigens appear.
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5The AB blood group in humans, where both A and B antigens are present, is an example of:
Incomplete Dominance and Codominance
Easy
A.Epistasis
B.Incomplete dominance
C.Codominance
D.Pleiotropy
Correct Answer: Codominance
Explanation:
In blood group AB, both and alleles are expressed fully, producing both antigens, which is codominance.
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6An allelic series refers to:
Allelic series
Easy
A.A sequence of amino acids in a protein
B.A group of multiple alleles of a single gene arranged by dominance
C.A set of chromosomes in a genome
D.A series of genes on the same chromosome
Correct Answer: A group of multiple alleles of a single gene arranged by dominance
Explanation:
An allelic series is a set of multiple alleles at one locus, often ranked in a dominance hierarchy, such as the coat color alleles in rabbits.
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7The coat color of rabbits controlled by the alleles , , , and is a classic example of:
Allelic series
Easy
A.An allelic series
B.Codominance only
C.Polygenic inheritance
D.Cytoplasmic inheritance
Correct Answer: An allelic series
Explanation:
Rabbit coat color is governed by a series of four alleles arranged in a dominance hierarchy, forming a well-known allelic series.
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8Epistasis is best defined as:
Gene Interactions: Epistasis and types
Easy
A.Genes located outside the nucleus
B.One gene masking the expression of another gene
C.A gene affecting multiple traits
D.Two alleles of the same gene interacting
Correct Answer: One gene masking the expression of another gene
Explanation:
Epistasis occurs when one gene at a locus masks or modifies the phenotypic expression of a different gene at another locus.
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9In recessive epistasis, the modified dihybrid ratio observed is:
Gene Interactions: Epistasis and types
Easy
A.12:3:1
B.9:7
C.15:1
D.9:3:4
Correct Answer: 9:3:4
Explanation:
Recessive epistasis produces a 9:3:4 ratio, where the homozygous recessive genotype at the epistatic locus masks the second gene's expression.
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10The gene whose expression is masked by another gene is called the:
Gene Interactions: Epistasis and types
Easy
A.Dominant gene
B.Modifier gene
C.Hypostatic gene
D.Epistatic gene
Correct Answer: Hypostatic gene
Explanation:
The gene that is masked is called hypostatic, while the gene that does the masking is called epistatic.
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11Pleiotropy refers to a condition where:
Pleiotropy
Easy
A.One gene masks another gene
B.A single gene affects multiple traits
C.Alleles show blending in heterozygotes
D.Multiple genes affect a single trait
Correct Answer: A single gene affects multiple traits
Explanation:
In pleiotropy, one gene influences several seemingly unrelated phenotypic characters, as seen in sickle-cell anemia.
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12Which of the following is a well-known example of pleiotropy in humans?
Pleiotropy
Easy
A.Skin color inheritance
B.Sickle-cell anemia
C.Snail shell coiling
D.ABO blood groups
Correct Answer: Sickle-cell anemia
Explanation:
Sickle-cell anemia is caused by a single gene mutation that produces multiple effects on the body, illustrating pleiotropy.
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13Genomic imprinting is a phenomenon in which:
Genomic imprinting
Easy
A.Genes are inherited only from the mother
B.Genes mutate during meiosis
C.Both alleles are always expressed equally
D.Gene expression depends on the parent of origin
Correct Answer: Gene expression depends on the parent of origin
Explanation:
In genomic imprinting, the expression of a gene depends on whether it is inherited from the mother or the father, due to epigenetic marking.
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14Genomic imprinting is primarily caused by which epigenetic mechanism?
Genomic imprinting
Easy
A.Gene duplication
B.Point mutation
C.DNA methylation
D.Chromosomal deletion
Correct Answer: DNA methylation
Explanation:
Genomic imprinting mainly results from DNA methylation, which silences one parental allele without changing the DNA sequence.
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15Penetrance is defined as:
Penetrance
Easy
A.The masking of one gene by another
B.The proportion of individuals with a genotype that show the expected phenotype
C.The degree to which a trait is expressed in an individual
D.The number of alleles at a locus
Correct Answer: The proportion of individuals with a genotype that show the expected phenotype
Explanation:
Penetrance measures the percentage of individuals carrying a particular genotype who actually express the associated phenotype.
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16Expressivity refers to:
Expressivity
Easy
A.The degree to which a genotype is phenotypically expressed
B.The percentage of individuals showing a trait
C.The location of a gene on a chromosome
D.The number of genes controlling a trait
Correct Answer: The degree to which a genotype is phenotypically expressed
Explanation:
Expressivity describes the range or intensity with which a particular genotype is expressed in individuals who show the trait.
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17Cytoplasmic inheritance involves genes located in:
Cytoplasmic Inheritance: Definition
Easy
A.The cell wall
B.Mitochondria and chloroplasts
C.The ribosomes
D.The nucleus only
Correct Answer: Mitochondria and chloroplasts
Explanation:
Cytoplasmic inheritance is controlled by genes present in cytoplasmic organelles such as mitochondria and chloroplasts, not the nucleus.
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18In humans, mitochondrial DNA is generally inherited from:
Inheritance of Mitochondrial DNA
Easy
A.Either parent randomly
B.The father only
C.The mother only
D.Both parents equally
Correct Answer: The mother only
Explanation:
Mitochondrial DNA is maternally inherited because the egg contributes the cytoplasm and mitochondria to the zygote, while sperm mitochondria are usually eliminated.
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19Chloroplast DNA is typically inherited in a pattern that is:
Inheritance of Chloroplast DNA
Easy
A.Only through pollen grains
B.Controlled entirely by nuclear genes
C.Uniparental and maternal in most plants
D.Strictly biparental in all plants
Correct Answer: Uniparental and maternal in most plants
Explanation:
In most plants, chloroplast DNA is maternally (uniparentally) inherited, being transmitted through the egg cytoplasm.
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20Streptomycin resistance in Chlamydomonas is an example of a trait inherited through:
Examples- Drug resistance in Chloroplast
Easy
A.Nuclear DNA
B.Mitochondrial DNA
C.Chloroplast DNA
D.Ribosomal RNA
Correct Answer: Chloroplast DNA
Explanation:
Streptomycin resistance in Chlamydomonas is a classic example of cytoplasmic inheritance carried by genes in the chloroplast DNA.
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21In the human ABO blood group system, which of the following genotypes would produce an individual with blood group AB?
Alleles: Multiple alleles
Medium
A.
B.
C.
D.
Correct Answer:
Explanation:
The AB blood group arises when both and alleles are present. Since and are codominant, both antigens A and B are expressed, giving blood group AB.
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22A cross between red-flowered () and white-flowered () snapdragons yields pink plants. If the plants are self-crossed, what phenotypic ratio is expected in the ?
Incomplete Dominance and Codominance
Medium
A.1 red : 2 pink : 1 white
B.9 : 3 : 3 : 1
C.3 red : 1 white
D.1 red : 1 white
Correct Answer: 1 red : 2 pink : 1 white
Explanation:
In incomplete dominance the heterozygote shows an intermediate phenotype. The genotypic ratio directly matches the phenotypic ratio 1 red : 2 pink : 1 white.
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23Which of the following best distinguishes codominance from incomplete dominance?
Incomplete Dominance and Codominance
Medium
A.In codominance the recessive allele dominates
B.In codominance only one allele is expressed
C.In codominance the heterozygote shows a blended intermediate phenotype
D.In codominance both alleles are fully and separately expressed in the heterozygote
Correct Answer: In codominance both alleles are fully and separately expressed in the heterozygote
Explanation:
Codominance results in simultaneous, distinct expression of both alleles (e.g., AB blood group), whereas incomplete dominance produces a blended intermediate phenotype (e.g., pink flowers).
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24In rabbit coat colour, the dominance order is . A rabbit with genotype would display which phenotype?
Allelic series
Medium
A.Albino
B.Full colour
C.Himalayan
D.Chinchilla
Correct Answer: Chinchilla
Explanation:
In an allelic series, an allele is expressed according to its rank in the dominance hierarchy. Since is dominant over , the genotype shows the chinchilla phenotype.
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25In a dihybrid cross, a modified ratio of 9 : 3 : 4 is observed. Which type of epistasis does this indicate?
Gene Interactions: Epistasis and types
Medium
A.Dominant epistasis
B.Dominant inhibitory epistasis
C.Recessive epistasis
D.Duplicate recessive epistasis
Correct Answer: Recessive epistasis
Explanation:
A 9 : 3 : 4 ratio is characteristic of recessive epistasis, where the recessive allele at one locus (in homozygous form) masks the expression of the second gene.
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26A dihybrid cross gives an ratio of 12 : 3 : 1. This modified ratio is produced by which form of epistasis?
Gene Interactions: Epistasis and types
Medium
A.Duplicate dominant epistasis
B.Recessive epistasis
C.Complementary gene interaction
D.Dominant epistasis
Correct Answer: Dominant epistasis
Explanation:
In dominant epistasis, a dominant allele at one locus masks the expression of the alleles at another locus, producing the modified 12 : 3 : 1 ratio.
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27The 9 : 7 ratio observed in sweet pea flower colour is best explained by which type of gene interaction?
In complementary gene interaction, dominant alleles of both genes are needed to produce colour. Any homozygous recessive condition gives white, yielding the 9 : 7 ratio.
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28Which of the following is the best example of pleiotropy?
Pleiotropy
Medium
A.Two genes together controlling comb shape in fowl
B.A dominant allele masking a gene at another locus
C.One trait controlled by many additive genes
D.A single gene in sickle-cell anaemia affecting anaemia, pain crises, and organ damage
Correct Answer: A single gene in sickle-cell anaemia affecting anaemia, pain crises, and organ damage
Explanation:
Pleiotropy is when a single gene influences multiple, seemingly unrelated phenotypic traits, as seen in sickle-cell anaemia where one mutation causes many effects.
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29Which statement best describes genomic imprinting?
Genomic imprinting
Medium
A.Imprinting alters the DNA base sequence of the gene
B.The maternal allele is always silenced
C.Gene expression depends on the parent of origin of the allele
D.Both parental alleles are always equally expressed
Correct Answer: Gene expression depends on the parent of origin of the allele
Explanation:
In genomic imprinting, an allele is expressed or silenced depending on whether it was inherited from the mother or father, without any change in the DNA sequence (an epigenetic effect).
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30Prader-Willi and Angelman syndromes are classic examples of genomic imprinting because they:
Genomic imprinting
Medium
A.Are caused by trisomy of chromosome 21
B.Result from codominant alleles
C.Result from deletions in the same chromosomal region but differ by parental origin
D.Arise from mitochondrial DNA mutations
Correct Answer: Result from deletions in the same chromosomal region but differ by parental origin
Explanation:
Both disorders involve the 15q11-q13 region. A paternal deletion causes Prader-Willi, while a maternal deletion causes Angelman, illustrating parent-of-origin effects.
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31If a dominant allele is present in 80 individuals but the associated phenotype is expressed in only 60, what is the penetrance?
Penetrance
Medium
A.60%
B.75%
C.133%
D.80%
Correct Answer: 75%
Explanation:
Penetrance is the proportion of individuals with a genotype that show the expected phenotype: .
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32Two individuals carry the same disease allele but one shows severe symptoms while the other shows only mild symptoms. This variation is described as:
Expressivity
Medium
A.Codominance
B.Pleiotropy
C.Incomplete penetrance
D.Variable expressivity
Correct Answer: Variable expressivity
Explanation:
Expressivity refers to the degree or intensity to which a genotype is phenotypically expressed. Different severity levels among affected individuals reflect variable expressivity.
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33Polydactyly shows incomplete penetrance. This means that some individuals who carry the dominant allele:
Penetrance
Medium
A.Always show extra digits on all limbs
B.Express the trait only in old age
C.Pass the trait only to daughters
D.Do not show extra digits at all
Correct Answer: Do not show extra digits at all
Explanation:
Incomplete penetrance means not all individuals carrying the allele express the trait. Some polydactyly carriers appear phenotypically normal despite having the dominant allele.
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34Which feature is most characteristic of cytoplasmic (extranuclear) inheritance?
Cytoplasmic Inheritance: Definition
Medium
A.Traits are typically inherited from the maternal parent
Correct Answer: Traits are typically inherited from the maternal parent
Explanation:
Cytoplasmic inheritance involves genes in mitochondria and plastids, which are transmitted mainly through the egg cytoplasm, resulting in maternal (uniparental) inheritance.
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35A mother affected by a mitochondrial disorder (such as Leber's hereditary optic neuropathy) is expected to transmit the condition to:
Inheritance of Mitochondrial DNA
Medium
A.Only her sons
B.Only her daughters
C.All of her children, regardless of sex
D.None of her children
Correct Answer: All of her children, regardless of sex
Explanation:
Mitochondria are inherited maternally, so an affected mother can pass the disorder to all her offspring. Affected fathers, however, do not transmit mitochondrial diseases.
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36Chloroplast DNA is generally inherited maternally in most angiosperms because:
Inheritance of Chloroplast DNA
Medium
A.Chloroplasts are found only in the nucleus
B.Pollen contains more chloroplasts than the egg
C.Chloroplast genes follow Mendelian dominance
D.The male gamete usually contributes little or no cytoplasm to the zygote
Correct Answer: The male gamete usually contributes little or no cytoplasm to the zygote
Explanation:
The egg cell contributes most of the cytoplasm and hence the plastids to the zygote, so chloroplast DNA is generally transmitted maternally.
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37Streptomycin resistance in Chlamydomonas is inherited in a non-Mendelian, uniparental manner. This is because the resistance gene is located in the:
Examples- Drug resistance in Chloroplast
Medium
A.Nuclear DNA
B.Ribosomal RNA of the cytoplasm
C.Chloroplast DNA
D.Golgi apparatus
Correct Answer: Chloroplast DNA
Explanation:
In Chlamydomonas, streptomycin resistance is encoded by chloroplast (plastid) DNA and is inherited from the parent, showing uniparental cytoplasmic inheritance.
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38In Mirabilis jalapa (four o'clock plant), the leaf variegation pattern of the offspring is determined by:
Four O'clock plant
Medium
A.The branch (maternal) type from which the female flower was taken
B.Equal contribution from both parents
C.The pollen source used in the cross
D.Nuclear dominant alleles
Correct Answer: The branch (maternal) type from which the female flower was taken
Explanation:
Korrens showed that offspring leaf colour in Mirabilis jalapa depends solely on the maternal branch (green, white, or variegated), reflecting plastid inheritance through the egg cytoplasm.
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39The killer trait in Paramecium requires kappa particles in the cytoplasm and a specific nuclear genotype. Which nuclear genotype is necessary to maintain kappa particles?
Kappa particles in Paramecium
Medium
A.Homozygous recessive
B.Presence of only allele
C.No nuclear gene is required
D.At least one dominant allele
Correct Answer: At least one dominant allele
Explanation:
Kappa particles (which produce the toxin paramecin) can only be maintained in the cytoplasm of Paramecium carrying the dominant nuclear allele . Without , kappa particles are lost.
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40In the snail Limnaea, shell coiling direction is a maternal effect trait. The phenotype of an individual is determined by:
Snail shell coiling
Medium
A.Its own genotype
B.The genotype of its mother
C.The genotype of its father
D.The cytoplasmic DNA of the mother
Correct Answer: The genotype of its mother
Explanation:
In Limnaea, coiling direction is controlled by nuclear genes but the phenotype is set by the mother's genotype (maternal effect), which determines the orientation of early cleavage in the egg.
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41In the ABO blood group system, a couple where one parent is blood group AB and the other is blood group O are told by a genetics lab that their child is blood group O. Assuming no laboratory error or mutation, what is the most likely genetic explanation?
Alleles: Multiple alleles
Hard
A.The AB parent contributed a silent recessive allele that recombined
B.Codominance failed to express in the child due to incomplete penetrance
C.The O parent carried a hidden genotype that was not detected serologically
D.The child possesses the rare Bombay (hh) phenotype masking an inherited A or B allele
Correct Answer: The child possesses the rare Bombay (hh) phenotype masking an inherited A or B allele
Explanation:
An AB × O cross cannot normally yield an O child, since the AB parent always transmits or . The Bombay phenotype (homozygous at the locus) prevents formation of the H antigen precursor, so A/B antigens cannot be displayed, phenotypically mimicking group O.
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42A single gene shows incomplete dominance for flower color (red RR, pink Rr, white rr) and simultaneously the same alleles are codominant for petal texture (R = smooth patch, r = rough patch, Rr = both patches). What phenotypic ratio for the combined traits is expected in the of an cross?
Incomplete Dominance and Codominance
Hard
A.1 : 1 : 1 : 1 for four independent phenotypic classes
B.3 red-smooth : 1 white-rough with no intermediates
Both trait expressions are governed by the same single gene with the same three genotypes (, , ) in a 1:2:1 ratio. Thus each genotype has one fixed combined phenotype: =red-smooth, =pink-mixed, =white-rough, giving 1:2:1.
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43In rabbits, the coat color allelic series follows dominance . A full-color rabbit () is crossed with a Himalayan rabbit and produces offspring in a 1 full : 1 Himalayan ratio. Which genotypes of the parents are consistent with this result?
Allelic series
Hard
A.
B.
C.
D.
Correct Answer:
Explanation:
A 1:1 ratio requires a test-cross-like configuration. produces gametes and ; crossed with Himalayan gives (full) and (Himalayan) in 1:1. The other combinations either produce Himalayan offspring only or additional phenotypic classes.
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44A dihybrid cross yields an ratio of 9 : 7. This modified ratio is diagnostic of which type of gene interaction?
A 9:7 ratio arises when dominant alleles of both genes are required together to produce the phenotype (complementary genes). Any homozygous recessive condition at either locus blocks the pathway, merging the 3 + 3 + 1 classes into a single 7 mutant category.
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45In a certain plant, gene A is epistatic such that produces white flowers regardless of the B locus, while allows B-locus expression ( = purple, = red). What ratio results from a dihybrid cross?
Gene Interactions: Epistasis and types
Hard
A.9 white : 3 purple : 4 red
B.13 white : 3 purple
C.9 purple : 3 red : 4 white
D.12 white : 3 purple : 1 red
Correct Answer: 12 white : 3 purple : 1 red
Explanation:
This is dominant epistasis. (both 9 and 3 = 12) are white. The remaining classes split into (3, purple) and (1, red), giving the classic 12:3:1 ratio.
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46Sickle-cell anemia is often cited as a classic example of pleiotropy. Which observation best demonstrates the pleiotropic nature of the allele?
Pleiotropy
Hard
A.The allele shows incomplete dominance in heterozygotes at the molecular level
B.A single -globin mutation causes anemia, pain crises, organ damage, and malaria resistance
C.Multiple independent genes each contribute a fraction to red cell shape
D.Environmental temperature modifies the degree of red cell sickling in patients
Correct Answer: A single -globin mutation causes anemia, pain crises, organ damage, and malaria resistance
Explanation:
Pleiotropy means one gene affects multiple, seemingly unrelated phenotypic traits. A single point mutation in the -globin gene produces diverse effects—anemia, vaso-occlusive crises, splenic and organ damage, and heterozygote malaria resistance—illustrating pleiotropy.
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47Prader-Willi syndrome and Angelman syndrome can both result from deletions in the same 15q11-q13 chromosomal region, yet produce very different phenotypes. What best explains this?
Genomic imprinting
Hard
A.The deletions cause codominant expression of two overlapping gene sets
B.Random X-inactivation determines which syndrome develops in each patient
C.The phenotype depends on the parental origin of the affected chromosome due to imprinting
D.Both syndromes require simultaneous mutation of maternal and paternal copies
Correct Answer: The phenotype depends on the parental origin of the affected chromosome due to imprinting
Explanation:
Genomic imprinting silences genes based on parental origin. A paternal 15q11-q13 deletion (maternal copy already silenced) causes Prader-Willi, while a maternal deletion (paternal copy silenced) causes Angelman. The parent-of-origin determines the phenotype.
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48A dominant allele causes a disorder with 70% penetrance. If a heterozygous () affected individual mates with an unaffected homozygous recessive () partner, what fraction of the offspring are expected to actually show the disorder?
Penetrance
Hard
A.0.35
B.0.30
C.0.70
D.0.50
Correct Answer: 0.35
Explanation:
Genotypically, half the offspring are (0.5). Of those carrying the allele, only 70% express it due to incomplete penetrance. Thus the affected fraction .
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49Two patients carry the identical mutant allele for neurofibromatosis, yet one shows only a few café-au-lait spots while the other has extensive tumors and skeletal deformities. This variation in the degree of phenotypic expression among individuals with the same genotype is best described as:
Expressivity
Hard
A.Incomplete dominance
B.Phenotypic pleiotropy
C.Reduced penetrance
D.Variable expressivity
Correct Answer: Variable expressivity
Explanation:
Expressivity refers to the intensity or extent to which a genotype is phenotypically expressed. When individuals with the same genotype show a range of phenotype severity, this is variable expressivity, distinct from penetrance (whether the trait appears at all).
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50Which of the following features would MOST strongly distinguish a case of cytoplasmic (extranuclear) inheritance from an autosomal recessive nuclear trait?
Cytoplasmic Inheritance: Definition
Hard
A.Male and female offspring are affected in equal 1:1 proportions
B.The trait skips generations and reappears in a 3:1 ratio
C.Reciprocal crosses give different results and offspring resemble the maternal parent
D.Affected individuals are always heterozygous for the causative allele
Correct Answer: Reciprocal crosses give different results and offspring resemble the maternal parent
Explanation:
Cytoplasmic inheritance is characterized by non-Mendelian patterns: reciprocal crosses yield different outcomes, and offspring phenotype follows the maternal parent because cytoplasm (and its organelles) is transmitted through the egg. Nuclear traits show identical reciprocal cross results.
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51A woman with a mitochondrial disorder (heteroplasmic mtDNA mutation) has several children. Which pattern is expected, and why can severity differ among her children?
Inheritance of Mitochondrial DNA
Hard
A.None of her children are affected since the mutation is paternally transmitted
B.Only her sons inherit the mutation because sperm lacks mitochondria
C.All children inherit the mutation, but severity varies due to random mitochondrial segregation (heteroplasmy)
D.Half her children inherit it following Mendelian 1:1 segregation
Correct Answer: All children inherit the mutation, but severity varies due to random mitochondrial segregation (heteroplasmy)
Explanation:
mtDNA is maternally inherited, so all children of an affected mother receive mutant mitochondria. Because cells contain a mixture of mutant and wild-type mtDNA (heteroplasmy), random partitioning during cell division gives different mutant loads, and severity depends on the threshold effect.
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52In most angiosperms, chloroplast DNA is maternally inherited. However, in some gymnosperms and a few angiosperms, chloroplasts can be paternally or biparentally transmitted. This variation is best attributed to:
Inheritance of Chloroplast DNA
Hard
A.The presence of chloroplast-specific meiotic recombination
B.Differences in whether plastids are included in and survive within the male gamete
C.Random assortment of chloroplasts on the metaphase plate during mitosis
D.Selective nuclear silencing of paternal chloroplast genes after fertilization
Correct Answer: Differences in whether plastids are included in and survive within the male gamete
Explanation:
Plastid inheritance patterns depend on whether plastids are physically transmitted through the sperm/pollen and whether they survive. In many angiosperms plastids are excluded from the generative cell, giving maternal inheritance; in conifers they are often paternally transmitted.
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53In Chlamydomonas, streptomycin resistance () is inherited through the chloroplast. In a cross between () and (), what is the expected outcome in the offspring, given that the parent transmits its chloroplast?
Examples- Drug resistance in Chloroplast
Hard
A.Nearly all progeny are , reflecting uniparental inheritance from the parent
B.All progeny are because resistance is recessive
C.Progeny show a 3 : 1 ratio in the generation
D.Progeny segregate 1 : 1 as in a Mendelian test cross
Correct Answer: Nearly all progeny are , reflecting uniparental inheritance from the parent
Explanation:
In Chlamydomonas, chloroplast genes are inherited uniparentally from the mating type. Since the parent is , essentially all progeny inherit resistance regardless of the parent's chloroplast genotype.
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54In Mirabilis jalapa (four o'clock plant), variegated branches bear green, white, and variegated regions. If flowers on a variegated branch are pollinated by pollen from a green branch, what phenotypes appear in the progeny?
Four O'clock plant
Hard
A.Only variegated progeny, matching the maternal branch exactly
B.A 1 green : 2 variegated : 1 white Mendelian ratio
C.Only green progeny, since the pollen carries green plastids
D.Green, white, and variegated progeny, depending on the egg's plastid composition
Correct Answer: Green, white, and variegated progeny, depending on the egg's plastid composition
Explanation:
Plastid inheritance in Mirabilis is maternal; pollen contributes no plastids. Eggs from a variegated branch may contain green plastids, white plastids, or a mixture, so progeny can be green, white, or variegated irrespective of the pollen source.
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55In Paramecium, killer strains carry cytoplasmic kappa particles and require the nuclear dominant gene to maintain them. During conjugation without cytoplasmic exchange, a killer (, with kappa) conjugates with a sensitive (, no kappa). What are the exconjugant phenotypes?
Kappa particles in Paramecium
Hard
A.Both exconjugants become sensitive due to loss of kappa in both
B.A 3 killer : 1 sensitive ratio appears among the caryonides
C.One exconjugant remains killer, the other becomes sensitive lacking kappa
D.Both exconjugants become killers because is dominant
Correct Answer: One exconjugant remains killer, the other becomes sensitive lacking kappa
Explanation:
Without cytoplasmic bridge exchange, kappa stays with the original killer cell. Both exconjugants become nuclear genotype, but only the one retaining kappa is a killer; the former sensitive lacks kappa and stays sensitive even though it now carries —kappa maintenance requires but alone cannot generate kappa.
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56In Limnaea, shell coiling is controlled by a maternal-effect gene where dextral (D) is dominant to sinistral (d). A genotypically snail displays dextral coiling. What must have been the genotype of this snail's mother?
Snail shell coiling
Hard
A.The mother's genotype cannot influence this trait at all
B.The mother carried at least one allele ( or )
C.The mother was necessarily and sinistral
D.The mother must have been homozygous dextral only
Correct Answer: The mother carried at least one allele ( or )
Explanation:
In maternal-effect inheritance, coiling direction is determined by the mother's genotype, not the individual's own. A snail that coils dextrally must have had a mother carrying a allele ( or ), whose gene product deposited in the egg directed dextral coiling.
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57A dihybrid self-cross produces an ratio of 9 : 3 : 4. Which mechanism explains the 4-class?
Gene Interactions: Epistasis and types
Hard
A.Duplicate dominant genes producing a 15:1 collapse
B.Complementary gene action requiring both dominants together
C.Dominant epistasis merging two dominant phenotype classes
D.Recessive epistasis: homozygous recessive at one locus masks the other locus
Correct Answer: Recessive epistasis: homozygous recessive at one locus masks the other locus
Explanation:
In recessive epistasis, the homozygous recessive genotype at the epistatic locus () masks expression of the other gene. The (3) and (1) classes become phenotypically identical, merging to 4, giving 9:3:4.
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58Suppose a gene has different alleles in a population. How many distinct genotypes (including both homozygous and heterozygous combinations) are theoretically possible at this locus?
Multiple alleles
Hard
A.
B.
C.
D.
Correct Answer:
Explanation:
With alleles, the number of homozygotes is and heterozygotes is . The total genotypes .
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59Which molecular mechanism is primarily responsible for establishing genomic imprinting, allowing a gene to be silenced according to its parent of origin during gametogenesis?
Genomic imprinting
Hard
A.Point mutations that permanently inactivate one parental allele
B.Meiotic crossing over that physically removes one parental copy
C.Differential DNA methylation of imprinting control regions in the parental germlines
D.Codominant transcription of both parental alleles at reduced levels
Correct Answer: Differential DNA methylation of imprinting control regions in the parental germlines
Explanation:
Imprinting is an epigenetic phenomenon established mainly through sex-specific DNA methylation (and associated chromatin modifications) at imprinting control regions during gametogenesis. This methylation mark silences the allele in a parent-of-origin-specific manner without altering the DNA sequence.
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60The 'threshold effect' in mitochondrial diseases explains why symptoms appear only when the proportion of mutant mtDNA exceeds a critical level. Why do tissues like brain and muscle typically manifest symptoms at lower mutant loads than others?
Inheritance of Mitochondrial DNA
Hard
A.They have high energy demands, so their oxidative phosphorylation capacity is exceeded sooner
B.They lack nuclear-encoded repair systems for mitochondrial genes
C.They contain fewer total mitochondria, amplifying the mutation effect
D.They preferentially replicate mutant mtDNA over wild-type copies
Correct Answer: They have high energy demands, so their oxidative phosphorylation capacity is exceeded sooner
Explanation:
The threshold at which mutant mtDNA causes dysfunction is lower in tissues with high ATP requirements (brain, muscle, heart). Their heavy reliance on oxidative phosphorylation means that even a moderate mutant load reduces energy output below what the tissue needs, triggering symptoms earlier.
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