Unit 4: Haploid Production, Somaclonal Variations and Plant Microbe Interactions - Practice Quiz

BTY540 — Plant Biotechnology 60 Questions
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1 Anther culture is a technique used to produce plants that are:

Haploid Production: anther culture Easy
A. Triploid
B. Tetraploid
C. Haploid
D. Diploid

2 In anther culture, the haploid plants develop from which cells?

Haploid Production: anther culture Easy
A. Root cells
B. Microspores
C. Egg cells
D. Somatic cells

3 The production of haploid plants from the male gametophyte (pollen/microspore) is called:

Haploid Production: production of haploid plants by androgenesis and gynogenesis Easy
A. Gynogenesis
B. Parthenogenesis
C. Androgenesis
D. Apogamy

4 The production of haploid plants from the female gametophyte is known as:

Haploid Production: production of haploid plants by androgenesis and gynogenesis Easy
A. Embryogenesis
B. Gynogenesis
C. Somatogenesis
D. Androgenesis

5 Ovule culture is mainly used to obtain haploids through:

Haploid Production: ovule culture Easy
A. Gynogenesis
B. Organogenesis
C. Micropropagation
D. Androgenesis

6 The phenomenon of pollen grains switching from the normal gametophytic pathway to the sporophytic pathway in anther culture results in:

Haploid Production: anther culture Easy
A. Seed germination
B. Embryoid formation
C. Fruit setting
D. Root nodulation

7 Doubling the chromosome number of a haploid plant produces a:

Haploid Production: application of haploids Easy
A. Aneuploid
B. Homozygous diploid
C. Triploid
D. Heterozygous diploid

8 Which chemical is most commonly used to double the chromosome number in haploid plants?

Haploid Production: application of haploids Easy
A. Gibberellin
B. Auxin
C. Colchicine
D. Cytokinin

9 A major advantage of using haploids in plant breeding is the rapid production of:

Haploid Production: application of haploids Easy
A. Polyploids
B. Hybrid vigour
C. Mutant fruits
D. Homozygous lines

10 Somaclonal variation refers to the genetic variation observed in plants regenerated through:

Somaclonal variations: methods and techniques for isolation and selection of the variants Easy
A. Layering
B. Grafting
C. Seed germination
D. Tissue culture

11 The term 'somaclone' was coined to describe plants derived from:

Somaclonal variations: methods and techniques for isolation and selection of the variants Easy
A. Germ cell cultures
B. Zygotes
C. Somatic cell cultures
D. Pollen grains

12 Variation arising specifically from cultured gametic (germ) cells is often referred to as:

Somaclonal variations: methods and techniques for isolation and selection of the variants Easy
A. Somaclonal variation
B. Epigenetic variation
C. Clonal variation
D. Gametoclonal variation

13 In vitro selection of somaclonal variants often uses a selective agent added to the medium such as:

Somaclonal variations: methods and techniques for isolation and selection of the variants Easy
A. Distilled water
B. A toxin or salt
C. Plain agar
D. Sucrose only

14 Somaclonal variation is useful in crop improvement mainly because it can generate plants with:

Somaclonal variations: applications of somaclonal variations Easy
A. Sterile pollen only
B. No genetic change
C. Disease resistance
D. Reduced yield

15 A limitation of somaclonal variation in crop improvement is that some variations are:

Somaclonal variations: applications of somaclonal variations Easy
A. Unstable and non-heritable
B. Permanent and fixed
C. Always heritable
D. Always beneficial

16 Which factor increases the frequency of somaclonal variation during tissue culture?

Somaclonal variations: applications of somaclonal variations Easy
A. Short culture duration
B. Cold storage of seeds
C. Prolonged callus culture
D. Low sucrose

17 In vitro plant-microbe interaction assays are performed under conditions that are:

In vitro Plant microbe interactions: assay development Easy
A. Random natural
B. Unsterilized soil
C. Aseptic and controlled
D. Open field only

18 A common purpose of in vitro plant-microbe assays is to study:

In vitro Plant microbe interactions: assay development Easy
A. Host-pathogen interactions
B. Soil erosion
C. Fruit ripening rates
D. Weather patterns

19 A key limitation of in vitro plant-microbe interaction studies is that they may not fully reflect:

In vitro Plant microbe interactions: limitations and applications Easy
A. Nutrient media
B. Sterile conditions
C. Controlled temperature
D. Natural field conditions

20 In vitro plant-microbe interaction techniques are widely applied to study beneficial associations such as:

In vitro Plant microbe interactions: limitations and applications Easy
A. Mycorrhiza and nitrogen fixation
B. Leaf senescence
C. Photosynthesis rate
D. Seed dormancy

21 In anther culture, the developmental stage of pollen most favorable for inducing androgenesis is usually the:

Haploid Production: anther culture Medium
A. Fully differentiated generative cell stage
B. Tetrad stage before microspore release
C. Uninucleate microspore stage
D. Mature trinucleate pollen stage

22 A researcher recovers many diploid and mixoploid plants from an anther culture instead of pure haploids. The most likely source of these diploids is:

Haploid Production: anther culture Medium
A. Contamination by fungal cells
B. Fusion of two microspore nuclei
C. Regeneration from somatic anther wall tissue
D. Delayed pollen germination

23 The essential difference between androgenesis and gynogenesis in haploid production is that:

Haploid Production: production of haploid plants by androgenesis and gynogenesis Medium
A. Androgenesis needs pollination while gynogenesis does not
B. Androgenesis occurs in vivo while gynogenesis occurs in vitro
C. Androgenesis produces diploids while gynogenesis produces haploids
D. Androgenesis uses the male gametophyte while gynogenesis uses the female gametophyte

24 Gynogenesis is often chosen over androgenesis for a particular crop when:

Haploid Production: production of haploid plants by androgenesis and gynogenesis Medium
A. The species is recalcitrant to anther/microspore culture
B. The plant produces abundant pollen
C. The anthers are large and easy to isolate
D. The pollen is at the uninucleate stage

25 Unpollinated ovary or ovule culture for haploid production must typically be initiated:

Haploid Production: ovule culture Medium
A. Only after seed set has begun
B. Several days after successful fertilization
C. When the ovules are fully mature and dormant
D. Around the time of anthesis before fertilization

26 The main advantage of using doubled haploids (DH) over conventional inbreeding in plant breeding is that DH lines:

Haploid Production: application of haploids Medium
A. Eliminate the need for any selection
B. Introduce new heterozygous alleles
C. Increase the ploidy level of the crop permanently
D. Achieve complete homozygosity in a single generation

27 Haploids are especially valuable for detecting recessive mutations because in a haploid:

Haploid Production: application of haploids Medium
A. Mutations occur at a higher frequency
B. Dominant alleles are suppressed
C. Every gene is present in two copies
D. Recessive alleles are directly expressed without masking

28 To convert a haploid plant into a fertile doubled haploid, the agent most commonly applied is:

Haploid Production: application of haploids Medium
A. Colchicine
B. 2,4-D
C. Ethylene
D. Gibberellic acid

29 Somaclonal variation is best defined as the genetic and epigenetic variation observed among plants that are:

Somaclonal variations: methods and techniques for isolation and selection of the variants Medium
A. Regenerated from cultured cells or tissues
B. Produced by sexual hybridization
C. Obtained through grafting
D. Derived from unfertilized gametes

30 A prolonged callus phase and higher levels of hormones such as 2,4-D during culture tend to:

Somaclonal variations: methods and techniques for isolation and selection of the variants Medium
A. Increase the frequency of somaclonal variation
B. Guarantee genetic uniformity of regenerants
C. Completely prevent chromosomal changes
D. Reduce the mutation rate to zero

31 To isolate cell lines resistant to a fungal toxin, the most direct in vitro strategy is:

Somaclonal variations: methods and techniques for isolation and selection of the variants Medium
A. Lowering the incubation temperature
B. Removing all hormones from the medium
C. Increasing the sucrose concentration
D. Adding the toxin to the medium as a selection pressure

32 A variant recovered in vitro that loses its altered trait after being transferred to selection-free medium is best described as showing:

Somaclonal variations: methods and techniques for isolation and selection of the variants Medium
A. Gene amplification
B. A chromosomal deletion
C. Epigenetic (non-heritable) variation
D. A stable point mutation

33 Which technique is most appropriate for confirming that a selected somaclone carries a true chromosomal number change?

Somaclonal variations: methods and techniques for isolation and selection of the variants Medium
A. Counting the number of flowers
B. Measuring plant height
C. Cytological chromosome counting (karyotyping)
D. Assessing leaf color visually

34 The disease-resistant sugarcane and potato somaclones developed commercially illustrate that somaclonal variation can be used to:

Somaclonal variations: applications of somaclonal variations Medium
A. Generate improved crop varieties with novel useful traits
B. Permanently sterilize crop plants
C. Prevent all genetic change in a clone
D. Convert diploids into haploids

35 For a micropropagation industry aiming to produce genetically uniform planting material, somaclonal variation is regarded as:

Somaclonal variations: applications of somaclonal variations Medium
A. A method of chromosome doubling
B. A way to induce flowering
C. An undesirable problem to be minimized
D. A beneficial goal to be maximized

36 Compared with conventional mutation breeding using chemical mutagens, an advantage of exploiting somaclonal variation is that it:

Somaclonal variations: applications of somaclonal variations Medium
A. Eliminates the need for any selection step
B. Guarantees a specific desired mutation
C. Always produces only dominant mutations
D. Can generate variability without applying an external mutagen

37 A key requirement when developing an in vitro dual-culture assay for a plant–pathogen interaction is:

In vitro Plant microbe interactions: assay development Medium
A. Excluding the host plant tissue entirely
B. Allowing random airborne microbes to colonize
C. Maintaining axenic (contaminant-free) conditions for both partners
D. Using open field soil directly in the dish

38 In an in vitro assay to screen for a beneficial plant growth-promoting rhizobacterium, the most relevant positive readout would be:

In vitro Plant microbe interactions: assay development Medium
A. Browning and necrosis of all tissues
B. Complete death of the plant tissue
C. Enhanced root and shoot growth of inoculated plantlets
D. Loss of sterility in the medium

39 A major limitation of studying plant–microbe interactions purely in vitro is that:

In vitro Plant microbe interactions: limitations and applications Medium
A. It is impossible to control the microbial species used
B. Sterile conditions cannot be achieved
C. No environmental factors can ever be varied
D. Results may not fully reflect complex field/soil conditions

40 In vitro establishment of mycorrhizal or Rhizobium associations with plantlets is primarily applied to:

In vitro Plant microbe interactions: limitations and applications Medium
A. Induce haploid embryo formation
B. Double the chromosome number of the host
C. Study infection mechanisms and produce biofertilizer inoculants
D. Permanently sterilize the host plant

41 In anther culture, the developmental stage of the microspore at the time of inoculation is critical for successful androgenesis. If anthers are cultured too late (after the first pollen mitosis with a well-developed generative cell), which outcome is most likely?

anther culture Hard
A. Increased frequency of haploid embryoids due to nutrient abundance
B. Direct conversion of the tapetum into embryogenic callus
C. Enhanced diploid embryo formation via spontaneous chromosome doubling
D. Predominant gametophytic development into normal pollen rather than sporophytic embryogenesis

42 A researcher obtains a high frequency of regenerated plants from anther culture but finds many are diploid and heterozygous rather than haploid. What is the most probable origin of these plants?

anther culture Hard
A. Fusion of two haploid microspores during culture
B. Spontaneous diploidization of haploid microspore-derived embryos
C. Somatic tissues of the anther wall (connective, filament) rather than the microspores
D. Endoreduplication limited to the epidermal cells of embryoids

43 Ovule culture is often preferred over embryo culture in certain wide crosses. What is the primary rationale for culturing the intact ovule rather than excising the embryo directly?

ovule culture Hard
A. Ovules contain higher endogenous cytokinin that suppresses embryo growth
B. Only ovule culture permits somatic embryogenesis from nucellar tissue
C. The embryo is too small/immature to excise and survives better within its natural nutritive environment
D. The integuments must be removed to allow gynogenesis to occur

44 Gynogenesis is used instead of androgenesis in species such as onion and sugar beet primarily because:

production of haploid plants by androgenesis and gynogenesis Hard
A. Androgenesis in these species yields very low response or albino regenerants, while the female gametophyte is more responsive
B. The female gametophyte doubles chromosomes spontaneously whereas microspores never do
C. Gynogenesis avoids the need for cold pretreatment entirely
D. Microspores in these species are triploid and cannot form haploids

45 The 'bulbosum method' in barley produces haploids through a mechanism distinct from anther culture. Which best describes this mechanism?

production of haploid plants by androgenesis and gynogenesis Hard
A. Doubling of the H. bulbosum genome to compensate for H. vulgare loss
B. Selective elimination of Hordeum bulbosum chromosomes after interspecific hybridization, leaving a haploid H. vulgare genome
C. Parthenogenetic development of unfertilized H. bulbosum eggs
D. Fusion of H. vulgare egg with two H. bulbosum sperm

46 Doubled haploid (DH) technology dramatically shortens breeding programs. Compared to conventional selfing to reach near-homozygosity, the key genetic advantage of DH lines is:

application of haploids Hard
A. Instant, complete homozygosity in a single generation, fixing recombinant gametes immediately
B. Elimination of all deleterious recessive alleles from the population
C. Increased recombination frequency during meiosis of the haploid
D. Guaranteed heterosis in the resulting lines

47 Why are haploids and doubled haploids especially powerful for mapping and selecting recessive mutations?

application of haploids Hard
A. Recessive alleles are expressed directly in the haploid because there is no dominant masking allele
B. Doubling converts recessive alleles into dominant ones
C. Haploids increase the mutation rate of recessive loci
D. Haploids undergo more crossing over, unmasking recessives

48 Cold pretreatment (e.g., 4°C) of anthers before culture improves androgenesis. The most widely accepted explanation for this stress effect is:

production of haploid plants by androgenesis and gynogenesis Hard
A. It increases endogenous auxin to trigger rooting
B. It degrades the tapetum to release stored gametophytic mRNA
C. It diverts microspores from the gametophytic to the sporophytic pathway by disrupting normal development and preserving viable microspores
D. It causes spontaneous doubling of the microspore chromosome number

49 A somaclonal variant selected in vitro for herbicide tolerance loses the trait after a few generations in the field. This 'epigenetic' variation is best distinguished from a true genetic mutation because it:

Somaclonal variations: methods and techniques for isolation and selection of the variants Hard
A. Follows Mendelian segregation ratios in progeny
B. Is non-heritable/unstable and reverts, lacking a stable change in DNA sequence
C. Persists indefinitely through meiosis
D. Can be mapped to a single nuclear locus

50 To isolate salt-tolerant somaclones, cells are cultured on medium with gradually increasing NaCl. A limitation of this positive in vitro selection strategy is that:

Somaclonal variations: methods and techniques for isolation and selection of the variants Hard
A. Selected cells cannot be regenerated into plants
B. NaCl selection guarantees single-gene tolerance every time
C. Tolerance expressed at the cellular level may not translate to whole-plant/field tolerance
D. Only dominant mutations can ever be recovered by stepwise selection

51 Somaclonal variation frequency generally increases with which culture condition, making it a double-edged sword in micropropagation?

Somaclonal variations: methods and techniques for isolation and selection of the variants Hard
A. Direct organogenesis from meristems with low hormone levels
B. Cryopreservation of shoot tips
C. Prolonged culture passages and a callus/disorganized phase, especially with high auxin like 2,4-D
D. Short culture cycles from axillary buds

52 The disease-resistant sugarcane and the tomato variety 'DNAP-17' are cited examples of somaclonal variation. The chief advantage of using somaclonal variation over conventional mutation breeding here is that it:

applications of somaclonal variations Hard
A. Generates novel variability without mutagens and can uncover useful traits directly among regenerants
B. Eliminates the need for any field selection
C. Ensures the variation is confined to a single target gene
D. Always produces a higher mutation frequency than gamma irradiation

53 A key criticism limiting the practical exploitation of somaclonal variation for crop improvement is that:

applications of somaclonal variations Hard
A. Much of the observed variation is random, uncontrolled, and often includes undesirable/deleterious changes
B. It requires transgenic technology to recover useful lines
C. It can only produce variation in ornamental species
D. The variation is always dominant and cannot be fixed

54 When developing an in vitro dual-culture assay to study a mycorrhizal symbiosis, a major methodological challenge with arbuscular mycorrhizal (AM) fungi specifically is that:

In vitro Plant microbe interactions: assay development Hard
A. AM fungi produce sexual spores only in liquid culture
B. AM fungi are obligate biotrophs and cannot be grown axenically without a living host root
C. AM fungi require complete darkness and anaerobic conditions to germinate
D. AM fungi overgrow the medium and kill the host within hours

55 In designing an in vitro assay to screen for biocontrol activity of a rhizobacterium against a fungal pathogen, the most rigorous positive readout that distinguishes true antagonism from mere nutrient competition is:

In vitro Plant microbe interactions: assay development Hard
A. Faster bacterial growth than the fungus on the plate
B. Any reduction in the fungal colony diameter on rich medium
C. A clear inhibition zone in dual culture combined with confirmation of a diffusible/volatile antifungal metabolite
D. Co-existence of both organisms without contact

56 A recognized limitation of studying plant–microbe interactions in vitro (axenic culture) rather than in soil is that:

In vitro Plant microbe interactions: limitations and applications Hard
A. Axenic culture prevents any gene expression changes in the host
B. The artificial system omits the complex soil microbiome and physicochemical factors, so results may not reflect natural interactions
C. In vitro systems always overestimate pathogen virulence tenfold
D. Sterile media cannot support any microbial growth

57 Ri T-DNA transformed 'hairy root' cultures are extensively used in in vitro plant–microbe studies. Their principal advantage for such research is that they:

In vitro Plant microbe interactions: limitations and applications Hard
A. Eliminate the need for any Agrobacterium in the system
B. Grow rapidly, are genetically stable, hormone-autonomous, and support AM fungal colonization in a controlled system
C. Secrete antibiotics that sterilize the medium automatically
D. Photosynthesize and thus need no carbon source

58 In doubled haploid production, colchicine is applied to double the chromosome number. If colchicine treatment is applied after several cell divisions of the haploid have already occurred, the likely consequence is:

production of haploid plants by androgenesis and gynogenesis Hard
A. Complete failure of any chromosome doubling
B. Uniform tetraploid tissue throughout the plant
C. Conversion of the plant into a stable aneuploid
D. Production of chimeric/mixoploid plants with both haploid and diploid sectors

59 Albinism is a frequent problem in cereal anther/microspore culture. The underlying cause of these albino regenerants is most often:

anther culture Hard
A. Excess cytokinin blocking chlorophyll synthesis reversibly
B. Loss of the entire nuclear genome during androgenesis
C. Deletions or rearrangements in the plastid (chloroplast) genome preventing chlorophyll development
D. Contamination by achlorophyllous bacteria

60 Consider a scenario where a somaclone shows an improved trait, but you must confirm it is a genuine, exploitable somaclonal variant. The most decisive evidence is that the trait:

applications of somaclonal variations Hard
A. Disappears when the plant is transferred to soil
B. Correlates with the concentration of 2,4-D in the medium
C. Appears only in the primary regenerant under culture conditions
D. Is stably transmitted to sexual progeny in a heritable, predictable manner