A.The tendency of genes on the same chromosome to be inherited together
B.The exchange of DNA between nonhomologous chromosomes
C.The separation of homologous chromosomes during meiosis
D.The independent inheritance of all genes in an organism
Correct Answer: The tendency of genes on the same chromosome to be inherited together
Explanation:
Genes located close together on the same chromosome tend to be transmitted together and are described as linked.
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2Which observation suggests that two genes are linked?
Linkage and its estimation
Easy
A.All four gamete types occur in equal proportions
B.Recombinant combinations occur in exactly half of the offspring
C.Parental combinations occur more often than recombinant combinations
D.Only dominant traits appear in the offspring
Correct Answer: Parental combinations occur more often than recombinant combinations
Explanation:
Linked genes usually produce more parental-type offspring because they tend to remain together during inheritance.
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3How is recombination frequency calculated?
Linkage and its estimation
Easy
A.
B.
C.
D.
Correct Answer:
Explanation:
Recombination frequency is the percentage of total offspring that show recombinant combinations.
Incorrect! Try again.
4What is the maximum observable recombination frequency between two genes?
Linkage and its estimation
Easy
A.
B.
C.
D.
Correct Answer:
Explanation:
A recombination frequency of indicates that genes behave as if they are unlinked.
Incorrect! Try again.
5During which stage of meiosis does crossing-over normally occur?
Crossing-over mechanism
Easy
A.Prophase I
B.Anaphase II
C.Telophase II
D.Metaphase I
Correct Answer: Prophase I
Explanation:
Crossing-over occurs during prophase I after homologous chromosomes pair.
Incorrect! Try again.
6Crossing-over usually involves an exchange between which structures?
Crossing-over mechanism
Easy
A.Nonsister chromatids of homologous chromosomes
B.Centromeres of homologous chromosomes
C.Chromatids of nonhomologous chromosomes
D.Sister chromatids of one chromosome
Correct Answer: Nonsister chromatids of homologous chromosomes
Explanation:
Crossing-over exchanges corresponding DNA segments between nonsister chromatids of paired homologous chromosomes.
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7What is a chiasma?
Crossing-over mechanism
Easy
A.A structure that produces spindle fibers
B.A point where a chromosome joins the nucleus
C.A region where sister chromatids attach permanently
D.A site where nonsister chromatids have exchanged segments
Correct Answer: A site where nonsister chromatids have exchanged segments
Explanation:
A chiasma is the visible point of contact associated with crossing-over between homologous chromosomes.
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8What is a major genetic result of crossing-over?
Crossing-over mechanism
Easy
A.Permanent gene inactivation
B.Identical gamete formation
C.Reduced chromosome number
D.Increased genetic variation
Correct Answer: Increased genetic variation
Explanation:
Crossing-over creates new combinations of alleles, increasing variation among gametes and offspring.
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9What information does a chromosome map primarily show?
Chromosome mapping
Easy
A.The exact number of proteins in a chromosome
B.The sequence of cell divisions in meiosis
C.The relative positions of genes on a chromosome
D.The relative sizes of different organisms
Correct Answer: The relative positions of genes on a chromosome
Explanation:
A chromosome map shows gene order and relative distances based mainly on recombination frequencies.
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10Which unit is commonly used for genetic map distance?
Chromosome mapping
Easy
A.Nanometer
B.Nucleotide
C.Centimorgan
D.Micrometer
Correct Answer: Centimorgan
Explanation:
Genetic map distance is measured in centimorgans, with centimorgan corresponding to about recombination.
Incorrect! Try again.
11Two genes have a recombination frequency of . What is their approximate map distance?
Chromosome mapping
Easy
A. cM
B. cM
C. cM
D. cM
Correct Answer: cM
Explanation:
For short genetic distances, a recombination frequency of is approximately equal to cM.
Incorrect! Try again.
12Which pair of genes is expected to have the lowest recombination frequency?
Chromosome mapping
Easy
A.Genes assorting independently
B.Genes located very close together
C.Genes located far apart
D.Genes on different chromosomes
Correct Answer: Genes located very close together
Explanation:
Crossing-over is less likely to occur between genes that are close together on the same chromosome.
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13Which chromosomal variation involves the loss of a chromosome segment?
Structural and numerical variations in chromosomes and their implications
Easy
A.Translocation
B.Deletion
C.Duplication
D.Inversion
Correct Answer: Deletion
Explanation:
A deletion removes part of a chromosome and may result in the loss of one or more genes.
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14Which chromosomal variation produces an extra copy of a chromosome segment?
Structural and numerical variations in chromosomes and their implications
Easy
A.Inversion
B.Translocation
C.Duplication
D.Deletion
Correct Answer: Duplication
Explanation:
Duplication occurs when a chromosome segment is copied, creating additional genetic material.
Incorrect! Try again.
15What occurs during a chromosomal inversion?
Structural and numerical variations in chromosomes and their implications
Easy
A.A segment is reversed within the chromosome
B.A whole chromosome is gained by the cell
C.A segment is removed from the chromosome
D.A chromosome set is lost from the cell
Correct Answer: A segment is reversed within the chromosome
Explanation:
In an inversion, a chromosome segment breaks, turns around, and reinserts in the opposite orientation.
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16What is aneuploidy?
Structural and numerical variations in chromosomes and their implications
Easy
A.Gain of one complete chromosome set
B.Reversal of a chromosome segment
C.Exchange between homologous chromatids
D.Gain or loss of individual chromosomes
Correct Answer: Gain or loss of individual chromosomes
Explanation:
Aneuploidy is a numerical variation involving one or more individual chromosomes rather than entire chromosome sets.
Incorrect! Try again.
17Which notation represents trisomy?
Structural and numerical variations in chromosomes and their implications
Easy
A.
B.
C.
D.
Correct Answer:
Explanation:
Trisomy means that one chromosome is present in three copies, giving a chromosome number of .
Incorrect! Try again.
18How many chromosome sets does a haploid cell contain?
Use of haploids, dihaploids, and double haploids in genetics
Easy
A.One set
B.Two sets
C.Four sets
D.Three sets
Correct Answer: One set
Explanation:
A haploid cell has one complete set of chromosomes, represented by .
Incorrect! Try again.
19Why are haploid organisms useful for studying recessive mutations?
Use of haploids, dihaploids, and double haploids in genetics
Easy
A.Haploid cells contain two copies of every allele
B.Recessive alleles are expressed without a dominant allele
C.Haploid cells prevent all mutations from occurring
D.Recessive alleles always become dominant after meiosis
Correct Answer: Recessive alleles are expressed without a dominant allele
Explanation:
Because haploids have only one allele per gene, a recessive mutation is not masked by a dominant allele.
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20What is a major advantage of double haploids in plant breeding?
Use of haploids, dihaploids, and double haploids in genetics
Easy
A.They increase crossing-over in every chromosome
B.They produce completely homozygous lines quickly
C.They eliminate all harmful genes from a population
D.They create new chromosome species immediately
Correct Answer: They produce completely homozygous lines quickly
Explanation:
Doubling the chromosomes of a haploid produces a double haploid that is homozygous at essentially every locus.
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21A testcross produces 800 offspring, of which 84 and 76 belong to the two recombinant classes. What is the estimated recombination frequency between the genes?
Linkage and its estimation
Medium
A.
B.
C.
D.
Correct Answer:
Explanation:
The recombination frequency is , indicating that the genes are approximately 20 map units apart.
Incorrect! Try again.
22An individual with genotype is testcrossed, and the most frequent offspring classes are and . What does this indicate about the arrangement of its alleles?
Linkage and its estimation
Medium
A.The genes occupy identical loci
B.The alleles are in coupling phase
C.The alleles are in repulsion phase
D.The genes assort independently
Correct Answer: The alleles are in coupling phase
Explanation:
In coupling, or cis, phase, both dominant alleles occur on one homolog and both recessive alleles occur on the other: .
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23Two genes show a recombination frequency close to . Which conclusion is most appropriate?
Linkage and its estimation
Medium
A.They must be on different chromosome arms
B.They must be tightly linked
C.They must occupy homologous loci
D.They may be unlinked or very far apart
Correct Answer: They may be unlinked or very far apart
Explanation:
A recombination frequency of is observed for independently assorting genes and can also occur when linked genes are so far apart that multiple crossovers obscure linkage.
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24At a proposed recombination fraction of , the LOD score for two genes is . How should this result be interpreted?
Linkage and its estimation
Medium
A.Independent assortment is supported at odds of
B.The genes must be exactly 10 base pairs apart and cannot undergo additional recombination events
C.Linkage is supported at odds of
D.Linkage is supported at odds of
Correct Answer: Linkage is supported at odds of
Explanation:
A LOD score of 3 means that linkage at the specified recombination fraction is , or 1000, times more likely than no linkage.
Incorrect! Try again.
25During which meiotic stage are homologous chromosomes fully synapsed and crossing-over primarily occurs?
Crossing-over mechanism
Medium
A.Leptotene of prophase I
B.Metaphase of meiosis I
C.Diplotene of prophase I
D.Pachytene of prophase I
Correct Answer: Pachytene of prophase I
Explanation:
Crossing-over occurs mainly during pachytene, when homologous chromosomes are fully paired through the synaptonemal complex.
Incorrect! Try again.
26A single crossover occurs between two nonsister chromatids of a homologous chromosome pair. What chromatids are expected at the end of meiosis?
Crossing-over mechanism
Medium
A.Two parental and two recombinant chromatids
B.Four recombinant chromatids of equal type
C.Four parental chromatids because sister chromatids remain associated throughout the entire meiotic division
D.Three parental and one recombinant chromatid
Correct Answer: Two parental and two recombinant chromatids
Explanation:
A single crossover involves only two of the four chromatids, producing two recombinant chromatids while the other two remain parental.
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27A mutation prevents the formation of programmed double-strand DNA breaks during early meiosis. Which outcome is most likely?
Crossing-over mechanism
Medium
A.Normal crossing-over but delayed cytokinesis
B.Reduced crossing-over and fewer chiasmata
C.Normal chiasma formation because meiotic recombination begins only after homologous chromosomes separate
D.Increased crossing-over and more chiasmata
Correct Answer: Reduced crossing-over and fewer chiasmata
Explanation:
Programmed double-strand breaks initiate meiotic recombination. Preventing them reduces crossover formation and therefore decreases the number of chiasmata.
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28What products commonly result from a crossover within the inverted segment of a paracentric inversion heterozygote?
Crossing-over mechanism
Medium
A.A pair of chromatids carrying equal terminal deletions
B.A dicentric chromatid and an acentric fragment
C.Two chromosomes with duplicated centromeres
D.Two normal chromatids with new allele combinations
Correct Answer: A dicentric chromatid and an acentric fragment
Explanation:
Crossing-over within a paracentric inversion loop can generate one dicentric recombinant chromatid and one acentric fragment, which are usually not transmitted normally.
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29In a three-point testcross, the most frequent classes are and , while the least frequent classes are and . Which gene lies in the middle?
Chromosome mapping
Medium
A.Gene
B.Gene
C.Genes and are inseparable
D.Gene
Correct Answer: Gene
Explanation:
The double-crossover classes differ from their corresponding parental classes only at gene , identifying as the middle gene.
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30A three-point testcross gives the following offspring: , , , , , , , and . What is the best map?
Chromosome mapping
Medium
A.
B.
C.
D.
Correct Answer:
Explanation:
The rare classes identify as the middle gene. The – distance is cM, and the – distance is cM.
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31Two adjacent map intervals are 10 cM and 20 cM. The observed double-crossover frequency is . What is the interference?
Chromosome mapping
Medium
A.
B.
C.
D.
Correct Answer:
Explanation:
The expected double-crossover frequency is . The coefficient of coincidence is , so interference is .
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32Genes , , and occur in that order, with distances of 12 cM between and and 8 cM between and . If crossovers occur independently, how many double-crossover offspring are expected among 5,000 progeny?
Chromosome mapping
Medium
A.96
B.480
C.48
D.24
Correct Answer: 48
Explanation:
The expected double-crossover frequency is . Thus, double-crossover offspring are expected.
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33A recessive allele becomes phenotypically expressed in a heterozygous individual because the homologous chromosome carries a deletion covering the normal dominant allele. What is this phenomenon called?
Structural and numerical variations in chromosomes and their implications
Medium
A.Allelic complementation
B.Pseudodominance
C.Incomplete penetrance
D.Gene dosage compensation
Correct Answer: Pseudodominance
Explanation:
A deletion can uncover a recessive allele on the intact homolog, causing it to be expressed as though it were dominant. This is called pseudodominance.
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34Why does a reciprocal translocation heterozygote often show reduced fertility despite having no net loss of genetic material?
Structural and numerical variations in chromosomes and their implications
Medium
A.Adjacent segregation produces duplication and deletion
B.Every gamete receives a complete balanced genome but becomes inviable because chromosome number alone changes
C.Alternate segregation always eliminates one chromosome
D.Homologous chromosomes fail to replicate before meiosis
Correct Answer: Adjacent segregation produces duplication and deletion
Explanation:
Adjacent segregation sends translocated and normal chromosomes into unbalanced gametes, creating partial duplications and deletions that often reduce viability.
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35A phenotypically normal person has 45 chromosomes because two acrocentric chromosomes have fused. Which condition best explains this observation?
Structural and numerical variations in chromosomes and their implications
Medium
A.A balanced Robertsonian translocation carrier
B.A complete autosomal monosomic individual with extensive compensatory gene amplification across the remaining chromosomes
C.A reciprocal deletion carrier
D.A paracentric inversion carrier
Correct Answer: A balanced Robertsonian translocation carrier
Explanation:
A balanced Robertsonian translocation joins the long arms of two acrocentric chromosomes. The carrier may have 45 chromosomes but retain nearly all essential genetic material.
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36A diploid species has . How many chromosomes would be present in a nullisomic individual and in a tetrasomic individual, respectively?
Structural and numerical variations in chromosomes and their implications
Medium
A.17 and 20
B.17 and 19
C.16 and 19
D.16 and 20
Correct Answer: 16 and 20
Explanation:
A nullisomic individual has chromosomes, while a tetrasomic individual has chromosomes.
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37An interspecific hybrid is sterile because its chromosomes lack homologous partners during meiosis. Which treatment is most likely to restore fertility?
Structural and numerical variations in chromosomes and their implications
Medium
A.Increasing recombination between nonhomologs
B.Doubling the complete chromosome complement
C.Producing several unrelated aneuploid lines
D.Deleting one chromosome from each genome
Correct Answer: Doubling the complete chromosome complement
Explanation:
Chromosome doubling gives each chromosome a homologous partner, allowing regular meiotic pairing and often producing a fertile allopolyploid.
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38A haploid plant produced by anther culture has genotype . Its chromosome complement is then doubled. What genotype will the resulting doubled haploid have?
Use of haploids, dihaploids, and double haploids in genetics
Medium
A.
B.
C.
D.
Correct Answer:
Explanation:
Chromosome doubling duplicates the single haploid genome. Therefore, the haploid becomes a completely homozygous doubled haploid.
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39A tetraploid crop has . A dihaploid is produced from it through haploidization. What chromosome number is expected in the dihaploid?
Use of haploids, dihaploids, and double haploids in genetics
Medium
A.48
B.12
C.18
D.24
Correct Answer: 24
Explanation:
A dihaploid derived from a tetraploid contains half of the tetraploid chromosome complement, so it has .
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40Why are haploid organisms especially useful for identifying recessive mutations?
Use of haploids, dihaploids, and double haploids in genetics
Medium
A.Recessive alleles are expressed without masking
B.Recessive alleles are converted into dominant alleles
C.Each haploid contains two homologous copies that allow recessive alleles to undergo complementation before expression
D.All mutations automatically increase chromosome number
Correct Answer: Recessive alleles are expressed without masking
Explanation:
A haploid has only one allele at each locus, so a recessive mutation is expressed directly rather than being masked by a dominant allele.
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41A testcross produces observed progeny , , , and . The class has viability relative to all other classes, whose viability is . What is the viability-corrected recombination fraction?
Linkage and its estimation
Hard
A.
B.
C.
D.
Correct Answer:
Explanation:
Correcting for viability gives . Thus .
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42An individual with linked loci in repulsion phase, , is testcrossed. If the recombination fraction is and reciprocal classes are equally frequent, what fraction of progeny will be ?
Linkage and its estimation
Hard
A.
B.
C.
D.
Correct Answer:
Explanation:
In repulsion, is a recombinant gamete. The two reciprocal recombinant classes each occur with frequency .
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43Two loci are physically on the same chromosome, but a very large testcross yields a recombination fraction near . Which conclusion is most defensible?
Linkage and its estimation
Hard
A.The loci must assort from different chromosomes
B.The loci must lie beside the same centromere
C.The loci may be far apart on one chromosome
D.The loci may show complete genetic linkage
Correct Answer: The loci may be far apart on one chromosome
Explanation:
Multiple crossovers can restore parental marker arrangements, causing widely separated linked loci to approach the recombination limit.
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44A linkage estimate from reciprocal testcrosses is through females but through males. Cytology confirms that the loci are separated physically. Which explanation best fits the result?
Linkage and its estimation
Hard
A.Female homologs undergo mitotic nondisjunction
B.Male meiosis lacks crossing-over in that region
C.Male gametes carry only parental chromosomes
D.Female meiosis converts every recombinant allele
Correct Answer: Male meiosis lacks crossing-over in that region
Explanation:
Sex-specific suppression or absence of crossing-over can produce zero male recombination despite physical separation of the loci.
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45A programmed meiotic double-strand break is repaired using the homolog, producing gene conversion but no reciprocal exchange of flanking markers. Which pathway most directly explains this outcome?
Synthesis-dependent strand annealing can copy information from the homolog and generate noncrossover gene conversion without exchanging chromosome arms.
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46In an ordered fungal octad, a locus displays a allele pattern while distant flanking markers retain their parental association. What event most directly produced the unusual segregation?
Crossing-over mechanism
Hard
A.Independent assortment at meiosis I
B.Mismatch repair within heteroduplex DNA
C.Centromere misdivision at meiosis II
D.Random chromatid loss after meiosis
Correct Answer: Mismatch repair within heteroduplex DNA
Explanation:
A pattern is a postmeiotic or conversion-type segregation signature arising from heteroduplex formation and mismatch processing.
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47Crossovers occur in two adjacent intervals with single-interval frequencies and . Among meioses, 120 double crossovers are observed. What is the coefficient of coincidence?
Crossing-over mechanism
Hard
A.
B.
C.
D.
Correct Answer:
Explanation:
Without interference, double crossovers are expected. The coefficient is .
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48A mutant forms meiotic double-strand breaks and invades homologous DNA normally, but cannot resolve double Holliday junctions through the crossover-biased pathway. Which phenotype is most likely?
Crossing-over mechanism
Hard
A.Absent breaks with normal crossover numbers
B.Normal crossovers with failed DNA replication
C.Increased crossovers with absent conversion
D.Reduced crossovers with retained noncrossovers
Correct Answer: Reduced crossovers with retained noncrossovers
Explanation:
Break formation and strand invasion can still support repair, but defective crossover resolution shifts products toward noncrossovers and reduces chiasmata.
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49A three-point testcross gives: , , , , , , , and . Which gene order and interval distances are supported?
Chromosome mapping
Hard
A.; cM and cM
B.; cM and cM
C.; cM and cM
D.; cM and cM
Correct Answer: ; cM and cM
Explanation:
The rare classes differ from the parentals only at , making central. Including double crossovers gives cM and cM.
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50For two loci, the observed recombination fraction is . Using Kosambi's mapping function , what is the estimated map distance?
Chromosome mapping
Hard
A. cM
B. cM
C. cM
D. cM
Correct Answer: cM
Explanation:
Substitution gives cM, slightly exceeding the raw recombinant percentage.
Incorrect! Try again.
51In ordered asci, a marker shows second-division segregation in of asci. Assuming standard ordered-tetrad interpretation, what is its distance from the centromere?
Chromosome mapping
Hard
A. cM
B. cM
C. cM
D. cM
Correct Answer: cM
Explanation:
Only half the chromatids are recombinant in a second-division segregation ascus, so distance is cM.
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52A testcross records recombination between and , between and , but only between and . What best explains why the outer-locus estimate is below ?
B.Gene conversion makes every crossover nonreciprocal
C.Centromere linkage eliminates single crossovers
D.Independent assortment reduces both interval distances
Correct Answer: Some double crossovers restore parental outer markers
Explanation:
Double crossovers can be recombinant in both internal intervals yet parental for the outer markers, causing two-point mapping to underestimate total distance.
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53A single crossover occurs within a paracentric inversion loop in a heterozygote. Which products are expected at anaphase I?
Structural and numerical variations in chromosomes and their implications
Hard
Correct Answer: A dicentric bridge and an acentric fragment
Explanation:
Crossing-over inside a paracentric inversion produces one dicentric recombinant and one acentric recombinant, usually making recombinant gametes inviable.
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54A phenotypically normal reciprocal-translocation heterozygote has high semisterility. Which meiotic segregation pattern most directly produces balanced gametes?
Structural and numerical variations in chromosomes and their implications
Hard
A.Random segregation of three centromeres
B.Alternate segregation of the quadrivalent
C.Adjacent-1 segregation of the quadrivalent
D.Adjacent-2 segregation of the quadrivalent
Correct Answer: Alternate segregation of the quadrivalent
Explanation:
Alternate segregation sends both normal chromosomes to one pole and both translocated chromosomes to the other, preserving overall gene dosage.
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55A recessive allele is unexpectedly expressed in a heterozygote, and cytology reveals a deletion spanning the homologous wild-type locus. What is this phenomenon?
Structural and numerical variations in chromosomes and their implications
Hard
A.Paramutation caused by allele conversion
B.Codominance caused by transvection
C.Overdominance caused by dosage increase
D.Pseudodominance caused by hemizygosity
Correct Answer: Pseudodominance caused by hemizygosity
Explanation:
The deletion removes the dominant wild-type allele, leaving the recessive allele unmasked in a hemizygous region.
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56For a centromere-linked marker, a disomic gamete from a heterozygous parent contains both alleles and . Which error most directly generated this gamete?
Structural and numerical variations in chromosomes and their implications
Hard
A.Sister nondisjunction at meiosis II
B.Centromere deletion after fertilization
C.Homolog nondisjunction at meiosis I
D.Chromatid breakage during pachytene
Correct Answer: Homolog nondisjunction at meiosis I
Explanation:
Meiosis I nondisjunction places both homologs in one gamete, producing heterodisomy with and near the centromere.
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57A locus near the end of an autotetraploid chromosome shows excess homozygosity relative to random chromosomal segregation. Which polysomic-meiosis feature best explains this pattern?
Structural and numerical variations in chromosomes and their implications
Hard
A.Mitotic recombination before floral induction
B.Double reduction after multivalent crossing-over
C.Dosage compensation after chromosome loss
D.Alternate segregation after translocation pairing
Correct Answer: Double reduction after multivalent crossing-over
Explanation:
Double reduction can place sister segments derived from one homolog into the same gamete, increasing homozygosity, especially at distal loci.
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58A doubled-haploid population is produced from an F1 with recombination fraction . Ignoring selection, what fraction of lines should be fixed as ?
Use of haploids, dihaploids, and double haploids in genetics
Hard
A.
B.
C.
D.
Correct Answer:
Explanation:
The recombinant haplotypes and each occur at ; chromosome doubling fixes each haplotype as a homozygous line.
Incorrect! Try again.
59A cultivated autotetraploid is crossed to a haploid inducer to recover plants with two chromosome sets from the cultivar. Why are these progeny called dihaploids?
Use of haploids, dihaploids, and double haploids in genetics
Hard
A.They arise by doubling a diploid embryo
B.They carry two extra inducer chromosomes
C.They are diploid relative to a tetraploid parent
D.They contain two identical paternal genomes
Correct Answer: They are diploid relative to a tetraploid parent
Explanation:
A dihaploid carries two basic chromosome sets, representing the haploid level of a tetraploid species while remaining cytologically diploid.
Incorrect! Try again.
60A recessive embryo-lethal allele cannot be recovered as a viable doubled-haploid line, although linked markers predict its transmission. Which stage most likely removes the genotype?
Use of haploids, dihaploids, and double haploids in genetics
Hard
A.Dominance restoration after marker genotyping
B.Haploid embryo development before chromosome doubling
C.Homolog pairing after complete line fixation
D.Independent assortment during doubled-line selfing
Correct Answer: Haploid embryo development before chromosome doubling
Explanation:
Haploids expose recessive alleles immediately. A lethal allele can eliminate the embryo before doubling creates a recoverable homozygous line.
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