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 exchange of DNA between nonhomologous chromosomes
B. The independent inheritance of all genes in an organism
C. The separation of homologous chromosomes during meiosis
D. The tendency of genes on the same chromosome to be inherited together

2 Which observation suggests that two genes are linked?

Linkage and its estimation Easy
A. Recombinant combinations occur in exactly half of the offspring
B. Parental combinations occur more often than recombinant combinations
C. All four gamete types occur in equal proportions
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. Metaphase I
D. Telophase II

6 Crossing-over usually involves an exchange between which structures?

Crossing-over mechanism Easy
A. Centromeres of homologous chromosomes
B. Nonsister chromatids of homologous chromosomes
C. Sister chromatids of one chromosome
D. Chromatids of nonhomologous chromosomes

7 What is a chiasma?

Crossing-over mechanism Easy
A. A region where sister chromatids attach permanently
B. A structure that produces spindle fibers
C. A point where a chromosome joins the nucleus
D. A site where nonsister chromatids have exchanged segments

8 What is a major genetic result of crossing-over?

Crossing-over mechanism Easy
A. Reduced chromosome number
B. Increased genetic variation
C. Permanent gene inactivation
D. Identical gamete formation

9 What information does a chromosome map primarily show?

Chromosome mapping Easy
A. The sequence of cell divisions in meiosis
B. The exact number of proteins in a chromosome
C. The relative sizes of different organisms
D. The relative positions of genes on a chromosome

10 Which unit is commonly used for genetic map distance?

Chromosome mapping Easy
A. Nucleotide
B. Centimorgan
C. Nanometer
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 located far apart
B. Genes assorting independently
C. Genes located very close together
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. Deletion
B. Duplication
C. Inversion
D. Translocation

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. Duplication
C. Translocation
D. Deletion

15 What occurs during a chromosomal inversion?

Structural and numerical variations in chromosomes and their implications Easy
A. A chromosome set is lost from the cell
B. A segment is removed from the chromosome
C. A whole chromosome is gained by the cell
D. A segment is reversed within the chromosome

16 What is aneuploidy?

Structural and numerical variations in chromosomes and their implications Easy
A. Exchange between homologous chromatids
B. Reversal of a chromosome segment
C. Gain of one complete chromosome set
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. Three sets
B. Two sets
C. One set
D. Four sets

19 Why are haploid organisms useful for studying recessive mutations?

Use of haploids, dihaploids, and double haploids in genetics Easy
A. Haploid cells prevent all mutations from occurring
B. Recessive alleles always become dominant after meiosis
C. Recessive alleles are expressed without a dominant allele
D. Haploid cells contain two copies of every allele

20 What is a major advantage of double haploids in plant breeding?

Use of haploids, dihaploids, and double haploids in genetics Easy
A. They eliminate all harmful genes from a population
B. They increase crossing-over in every chromosome
C. They create new chromosome species immediately
D. They produce completely homozygous lines quickly

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 assort independently
B. The alleles are in repulsion phase
C. The alleles are in coupling phase
D. The genes occupy identical loci

23 Two genes show a recombination frequency close to . Which conclusion is most appropriate?

Linkage and its estimation Medium
A. They may be unlinked or very far apart
B. They must be on different chromosome arms
C. They must be tightly linked
D. They must occupy homologous loci

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. Diplotene of prophase I
C. Metaphase of meiosis 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. Four parental chromatids because sister chromatids remain associated throughout the entire meiotic division
B. Three parental and one recombinant chromatid
C. Two parental and two recombinant chromatids
D. Four recombinant chromatids of equal type

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. Reduced crossing-over and fewer chiasmata
B. Normal crossing-over but delayed cytokinesis
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 dicentric chromatid and an acentric fragment
B. Two normal chromatids with new allele combinations
C. A pair of chromatids carrying equal terminal deletions
D. Two chromosomes with duplicated centromeres

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. Genes and are inseparable
C. Gene
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. 24
B. 48
C. 96
D. 480

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. Incomplete penetrance
B. Gene dosage compensation
C. Pseudodominance
D. Allelic complementation

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. Alternate segregation always eliminates one chromosome
B. Homologous chromosomes fail to replicate before meiosis
C. Every gamete receives a complete balanced genome but becomes inviable because chromosome number alone changes
D. Adjacent segregation produces duplication and deletion

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 complete autosomal monosomic individual with extensive compensatory gene amplification across the remaining chromosomes
B. A reciprocal deletion carrier
C. A balanced Robertsonian translocation 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. 16 and 19
B. 17 and 19
C. 17 and 20
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. Doubling the complete chromosome complement
B. Increasing recombination between nonhomologs
C. Deleting one chromosome from each genome
D. Producing several unrelated aneuploid lines

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. 24
B. 18
C. 48
D. 12

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 converted into dominant alleles
B. Each haploid contains two homologous copies that allow recessive alleles to undergo complementation before expression
C. Recessive alleles are expressed without masking
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 may be far apart on one chromosome
C. The loci may show complete genetic linkage
D. The loci must lie beside the same centromere

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. Male meiosis lacks crossing-over in that region
B. Female meiosis converts every recombinant allele
C. Female homologs undergo mitotic nondisjunction
D. Male gametes carry only parental chromosomes

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

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. Centromere misdivision at meiosis II
B. Mismatch repair within heteroduplex DNA
C. Independent assortment at meiosis I
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. Reduced crossovers with retained noncrossovers
B. Absent breaks with normal crossover numbers
C. Increased crossovers with absent conversion
D. Normal crossovers with failed DNA replication

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

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

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. Adjacent-1 segregation of the quadrivalent
B. Alternate segregation of the quadrivalent
C. Random segregation of three centromeres
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. Chromatid breakage during pachytene
B. Homolog nondisjunction at meiosis I
C. Centromere deletion after fertilization
D. Sister nondisjunction at meiosis II

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. Alternate segregation after translocation pairing
B. Dosage compensation after chromosome loss
C. Double reduction after multivalent crossing-over
D. Mitotic recombination before floral induction

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 contain two identical paternal genomes
B. They carry two extra inducer chromosomes
C. They are diploid relative to a tetraploid parent
D. They arise by doubling a diploid embryo

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. Haploid embryo development before chromosome doubling
B. Homolog pairing after complete line fixation
C. Independent assortment during doubled-line selfing
D. Dominance restoration after marker genotyping