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. Diploid
B. Haploid
C. Tetraploid
D. Triploid

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

Haploid Production: anther culture Easy
A. Egg cells
B. Root cells
C. Microspores
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. Androgenesis
B. Gynogenesis
C. Parthenogenesis
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. Somatogenesis
C. Androgenesis
D. Gynogenesis

5 Ovule culture is mainly used to obtain haploids through:

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

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. Fruit setting
C. Root nodulation
D. Embryoid formation

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

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

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

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

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

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

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. Tissue culture
B. Grafting
C. Layering
D. Seed germination

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. Somatic cell cultures
C. Zygotes
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. Clonal variation
B. Somaclonal variation
C. Epigenetic 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. A toxin or salt
B. Distilled water
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. No genetic change
B. Disease resistance
C. Sterile pollen only
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. Always beneficial
C. Always heritable
D. Permanent and fixed

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

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

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

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

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. Fruit ripening rates
C. Soil erosion
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. Natural field conditions
C. Controlled temperature
D. Sterile 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. Seed dormancy
D. Photosynthesis rate

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. Uninucleate microspore stage
C. Tetrad stage before microspore release
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. Delayed pollen germination
C. Regeneration from somatic anther wall tissue
D. Fusion of two microspore nuclei

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 uses the male gametophyte while gynogenesis uses the female gametophyte
B. Androgenesis needs pollination while gynogenesis does not
C. Androgenesis occurs in vivo while gynogenesis occurs in vitro
D. Androgenesis produces diploids while gynogenesis produces haploids

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 pollen is at the uninucleate stage
B. The species is recalcitrant to anther/microspore culture
C. The anthers are large and easy to isolate
D. The plant produces abundant pollen

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

Haploid Production: ovule culture Medium
A. Several days after successful fertilization
B. When the ovules are fully mature and dormant
C. Only after seed set has begun
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. Increase the ploidy level of the crop permanently
C. Achieve complete homozygosity in a single generation
D. Introduce new heterozygous alleles

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. Every gene is present in two copies
C. Recessive alleles are directly expressed without masking
D. Dominant alleles are suppressed

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. Ethylene
C. 2,4-D
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. Derived from unfertilized gametes
B. Regenerated from cultured cells or tissues
C. Obtained through grafting
D. Produced by sexual hybridization

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. Reduce the mutation rate to zero
B. Increase the frequency of somaclonal variation
C. Completely prevent chromosomal changes
D. Guarantee genetic uniformity of regenerants

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. Epigenetic (non-heritable) variation
B. Gene amplification
C. A chromosomal deletion
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. Assessing leaf color visually
C. Measuring plant height
D. Cytological chromosome counting (karyotyping)

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. Convert diploids into haploids
C. Permanently sterilize crop plants
D. Prevent all genetic change in a clone

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. An undesirable problem to be minimized
B. A beneficial goal to be maximized
C. A way to induce flowering
D. A method of chromosome doubling

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. Can generate variability without applying an external mutagen
B. Eliminates the need for any selection step
C. Guarantees a specific desired mutation
D. Always produces only dominant mutations

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. Allowing random airborne microbes to colonize
B. Using open field soil directly in the dish
C. Excluding the host plant tissue entirely
D. Maintaining axenic (contaminant-free) conditions for both partners

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. Loss of sterility in the medium
B. Browning and necrosis of all tissues
C. Complete death of the plant tissue
D. Enhanced root and shoot growth of inoculated plantlets

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. Double the chromosome number of the host
B. Induce haploid embryo formation
C. Permanently sterilize the host plant
D. Study infection mechanisms and produce biofertilizer inoculants

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

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. Spontaneous diploidization of haploid microspore-derived embryos
B. Somatic tissues of the anther wall (connective, filament) rather than the microspores
C. Fusion of two haploid microspores during culture
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. The integuments must be removed to allow gynogenesis to occur
B. Ovules contain higher endogenous cytokinin that suppresses embryo growth
C. Only ovule culture permits somatic embryogenesis from nucellar tissue
D. The embryo is too small/immature to excise and survives better within its natural nutritive environment

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. Gynogenesis avoids the need for cold pretreatment entirely
B. Androgenesis in these species yields very low response or albino regenerants, while the female gametophyte is more responsive
C. The female gametophyte doubles chromosomes spontaneously whereas microspores never do
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. Increased recombination frequency during meiosis of the haploid
B. Instant, complete homozygosity in a single generation, fixing recombinant gametes immediately
C. Guaranteed heterosis in the resulting lines
D. Elimination of all deleterious recessive alleles from the population

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

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

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

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. Persists indefinitely through meiosis
B. Can be mapped to a single nuclear locus
C. Is non-heritable/unstable and reverts, lacking a stable change in DNA sequence
D. Follows Mendelian segregation ratios in progeny

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. Only dominant mutations can ever be recovered by stepwise selection
B. NaCl selection guarantees single-gene tolerance every time
C. Selected cells cannot be regenerated into plants
D. Tolerance expressed at the cellular level may not translate to whole-plant/field tolerance

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. Prolonged culture passages and a callus/disorganized phase, especially with high auxin like 2,4-D
C. Cryopreservation of shoot tips
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. Eliminates the need for any field selection
B. Generates novel variability without mutagens and can uncover useful traits directly among regenerants
C. Always produces a higher mutation frequency than gamma irradiation
D. Ensures the variation is confined to a single target gene

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. The variation is always dominant and cannot be fixed
C. It requires transgenic technology to recover useful lines
D. It can only produce variation in ornamental species

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 are obligate biotrophs and cannot be grown axenically without a living host root
B. AM fungi produce sexual spores only in liquid culture
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. A clear inhibition zone in dual culture combined with confirmation of a diffusible/volatile antifungal metabolite
C. Any reduction in the fungal colony diameter on rich medium
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. In vitro systems always overestimate pathogen virulence tenfold
C. The artificial system omits the complex soil microbiome and physicochemical factors, so results may not reflect natural interactions
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. Grow rapidly, are genetically stable, hormone-autonomous, and support AM fungal colonization in a controlled system
B. Secrete antibiotics that sterilize the medium automatically
C. Photosynthesize and thus need no carbon source
D. Eliminate the need for any Agrobacterium in the system

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

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. Contamination by achlorophyllous bacteria
C. Loss of the entire nuclear genome during androgenesis
D. Deletions or rearrangements in the plastid (chloroplast) genome preventing chlorophyll development

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