Unit 5: Linkage, chromosome mapping and chromosomal variations in genetics - Practice Quiz

GPB203 — Principles Of Genetics 60 Questions
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1 What is genetic linkage?

Linkage and its estimation Easy
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

2 Which 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

3 How is recombination frequency calculated?

Linkage and its estimation Easy
A.
B.
C.
D.

4 What is the maximum observable recombination frequency between two genes?

Linkage and its estimation Easy
A.
B.
C.
D.

5 During 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

6 Crossing-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

7 What 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

8 What 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

9 What 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

10 Which unit is commonly used for genetic map distance?

Chromosome mapping Easy
A. Nanometer
B. Nucleotide
C. Centimorgan
D. Micrometer

11 Two genes have a recombination frequency of . What is their approximate map distance?

Chromosome mapping Easy
A. cM
B. cM
C. cM
D. cM

12 Which 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

13 Which 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

14 Which 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

15 What 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

16 What 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

17 Which notation represents trisomy?

Structural and numerical variations in chromosomes and their implications Easy
A.
B.
C.
D.

18 How 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

19 Why 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

20 What 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

21 A 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.

22 An 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

23 Two 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

24 At 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

25 During 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

26 A 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

27 A 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

28 What 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

29 In 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

30 A three-point testcross gives the following offspring: , , , , , , , and . What is the best map?

Chromosome mapping Medium
A.
B.
C.
D.

31 Two 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.

32 Genes , , 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

33 A 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

34 Why 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

35 A 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

36 A 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

37 An 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

38 A 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.

39 A 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

40 Why 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

41 A 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.

42 An 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.

43 Two 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

44 A 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

45 A 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?

Crossing-over mechanism Hard
A. Centromeric kinetochore co-orientation
B. Synthesis-dependent strand annealing
C. Nonhomologous chromosome end joining
D. Sister-chromatid cohesion establishment

46 In 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

47 Crossovers 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.

48 A 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

49 A 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

50 For 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

51 In 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

52 A testcross records recombination between and , between and , but only between and . What best explains why the outer-locus estimate is below ?

Chromosome mapping Hard
A. Some double crossovers restore parental outer markers
B. Gene conversion makes every crossover nonreciprocal
C. Centromere linkage eliminates single crossovers
D. Independent assortment reduces both interval distances

53 A 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
A. Two chromatids carrying reciprocal translocations
B. A ring chromosome and a centric fragment
C. Four chromatids with balanced duplications
D. A dicentric bridge and an acentric fragment

54 A 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

55 A 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

56 For 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

57 A 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

58 A 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.

59 A 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

60 A 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