Skip to main content

Exploitation of Somaclonal and Gametoclonal Variations for Plant Improvement


Exploitation of Somaclonal and Gametoclonal Variations for Plant Improvement 


1. Introduction


Plant tissue culture often induces genetic and epigenetic variations among regenerated plants. These variations, when stable and heritable, can be exploited as a source of novel traits for crop improvement.
Somaclonal variation: Variation arising in plants regenerated from somatic cells cultured in vitro.
Gametoclonal variation: Variation arising in plants regenerated from gametic cells (anther, pollen, ovule culture).
Both provide additional genetic variability beyond conventional breeding.


2. Somaclonal Variation


2.1 Definition
Somaclonal variation refers to genetic variation observed among plants regenerated from somatic tissue cultures, such as callus, suspension cultures, or explants.
Term coined by Larkin and Scowcroft (1981).
2.2 Sources of Somaclonal Variation
Chromosomal changes
Aneuploidy
Polyploidy
Chromosome rearrangements
Gene mutations
Point mutations
Insertions and deletions
Epigenetic changes
DNA methylation
Gene silencing
Transposable element activation
Culture-induced stress
Growth regulators
Prolonged subculturing
2.3 Detection of Somaclonal Variation
Morphological markers
Cytological analysis (karyotyping)
Biochemical markers (isozymes)
Molecular markers (RAPD, AFLP, SSR)
Field evaluation
3. Exploitation of Somaclonal Variation in Plant Improvement
3.1 Disease Resistance
Selection of resistant variants using pathogen toxins or filtrates
Examples:
Sugarcane – resistance to red rot
Banana – resistance to Fusarium wilt
Potato – resistance to late blight
3.2 Abiotic Stress Tolerance
Selection under stress conditions:
Salinity
Drought
Heavy metals
Examples:
Rice – salt tolerant somaclones
Wheat – drought tolerance
3.3 Herbicide Resistance
Selection using herbicides in culture media
Examples:
Tobacco – atrazine resistance
Maize – herbicide tolerant lines
3.4 Yield and Quality Improvement
Enhanced biomass
Improved sugar content
Modified starch or protein composition
Example:
Sugarcane somaclones with higher sucrose content
3.5 Horticultural Traits
Flower color variation
Altered plant architecture
Compact growth habit
Ornamentals: Chrysanthemum, Begonia
4. Gametoclonal Variation
4.1 Definition
Gametoclonal variation refers to genetic variation observed among plants regenerated from gametic cells, especially haploid or doubled haploid plants produced via anther or pollen culture.
4.2 Origin of Gametoclonal Variation
Meiotic recombination
Chromosome elimination
Mutations during gametophyte culture
Spontaneous or induced chromosome doubling
4.3 Methods Producing Gametoclonal Variation
Anther culture
Pollen (microspore) culture
Ovule / ovary culture


5. Exploitation of Gametoclonal Variation


5.1 Rapid Production of Homozygous Lines
Haploids → doubled haploids
Shortens breeding cycle
Used in:
Rice
Wheat
Barley
5.2 Selection for Recessive Traits
Direct expression of recessive alleles
No masking by dominant alleles
5.3 Stress Tolerance
Screening gametic cultures under stress
Examples:
Salt tolerance in rice
Cold tolerance in barley
5.4 Disease Resistance
Selection against pathogen toxins
Development of resistant pure lines

7. Advantages of Exploitation


Generates novel genetic variability
Useful for clonal crops
Faster than conventional breeding
Allows in vitro selection
Useful for traits difficult to select in field


8. Limitations
Unpredictable nature of variation
Some variations are unstable
Possibility of undesirable traits
Extensive field evaluation required
Technical expertise needed

9. Future Prospects


Integration with molecular markers
Use in genome editing and functional genomics
Marker-assisted selection of somaclones
Development of climate-resilient crops


10. Conclusion

Exploitation of somaclonal and gametoclonal variations provides a powerful complementary approach to conventional breeding. When combined with in vitro selection and molecular tools, these variations can significantly contribute to crop improvement, stress tolerance, and yield enhancement.



50 MCQs: Somaclonal & Gametoclonal Variation


1. Somaclonal variation refers to
A. Variation in seed progeny
B. Variation in sexually reproduced plants
C. Variation in plants regenerated from somatic tissue culture
D. Variation caused by hybridization
Answer: C
2. The term somaclonal variation was coined by
A. Murashige and Skoog
B. White
C. Larkin and Scowcroft
D. Haberlandt
Answer: C
3. Gametoclonal variation arises from
A. Somatic embryos
B. Callus cultures
C. Gametic tissues
D. Zygotic embryos
Answer: C
4. Which culture technique mainly produces gametoclonal variation?
A. Callus culture
B. Anther culture
C. Protoplast culture
D. Embryo culture
Answer: B
5. Somaclonal variation is most common in
A. Seed propagated crops
B. Vegetatively propagated crops
C. Forest trees only
D. Algae
Answer: B
6. Which of the following is NOT a source of somaclonal variation?
A. Chromosomal rearrangement
B. DNA methylation
C. Meiosis
D. Point mutation
Answer: C
7. Chromosomal variation includes
A. Polyploidy
B. Aneuploidy
C. Translocations
D. All of the above
Answer: D
8. Epigenetic variation mainly involves
A. Gene deletion
B. DNA methylation
C. Chromosome loss
D. Crossing over
Answer: B
9. Prolonged subculturing increases
A. Genetic stability
B. Somaclonal variation
C. Homozygosity
D. Fertility
Answer: B
10. Somaclonal variation is exploited mainly for
A. Clonal uniformity
B. Creating variability
C. Preventing mutation
D. Hybrid seed production
Answer: B
11. In vitro selection is used for
A. Eliminating variation
B. Selecting desired variants
C. Preventing regeneration
D. Seed dormancy
Answer: B
12. Disease resistance can be selected using
A. Growth hormones
B. Pathogen toxins
C. Vitamins
D. Sugars
Answer: B
13. Sugarcane somaclones are commonly selected for
A. Dwarfness
B. High sucrose content
C. Seedlessness
D. Early flowering
Answer: B
14. Herbicide resistance is selected by
A. Increasing light
B. Adding herbicide to medium
C. Changing temperature
D. Reducing nutrients
Answer: B
15. Tobacco somaclones have shown resistance to
A. Glyphosate
B. Atrazine
C. Paraquat
D. 2,4-D
Answer: B
16. Salinity tolerance can be selected by adding
A. NaCl to medium
B. Sucrose
C. Agar
D. Auxins
Answer: A
17. Gametoclonal variation is useful for
A. Producing heterozygous plants
B. Producing homozygous lines
C. Clonal propagation
D. Preventing recombination
Answer: B
18. Haploid plants are produced from
A. Somatic cells
B. Zygotes
C. Gametes
D. Endosperm
Answer: C
19. Doubled haploids are produced by
A. Chromosome elimination
B. Chromosome doubling
C. Mutation
D. Hybridization
Answer: B
20. Advantage of haploid plants
A. High heterozygosity
B. Direct expression of recessive traits
C. Genetic instability
D. Polyploidy
Answer: B
21. Gametoclonal variation shortens
A. Culture duration
B. Breeding cycle
C. Plant height
D. Seed dormancy
Answer: B
22. Which crop is widely improved using anther culture?
A. Rice
B. Cotton
C. Potato
D. Sugarcane
Answer: A
23. Which variation is more predictable?
A. Somaclonal
B. Gametoclonal
C. Spontaneous
D. Somatic mutation
Answer: B
24. Somaclonal variation is generally
A. Always stable
B. Unpredictable
C. Always beneficial
D. Always harmful
Answer: B
25. Molecular markers used to detect variation include
A. RAPD
B. AFLP
C. SSR
D. All of the above
Answer: D
26. Field evaluation is required to test
A. Culture medium
B. Genetic stability
C. Nutrient uptake
D. Callus growth
Answer: B
27. Ornamentals showing somaclonal variation include
A. Wheat
B. Chrysanthemum
C. Rice
D. Maize
Answer: B
28. Somaclonal variation is less useful in
A. Clonal crops
B. Vegetative crops
C. Seed propagated crops
D. Ornamentals
Answer: C
29. Activation of transposable elements causes
A. Genetic uniformity
B. Genetic instability
C. Chromosome doubling
D. Cell death
Answer: B
30. Somaclonal variation was first observed in
A. Animal cell culture
B. Plant tissue culture
C. Microbial culture
D. Fungal culture
Answer: B
31. Abiotic stress tolerance includes
A. Disease resistance
B. Insect resistance
C. Salinity tolerance
D. Pathogen resistance
Answer: C
32. Which is a limitation of somaclonal variation?
A. Generates variability
B. Low cost
C. Unstable traits
D. Rapid multiplication
Answer: C
33. Gametoclonal plants are usually
A. Polyploid
B. Heterozygous
C. Homozygous
D. Sterile
Answer: C
34. Ovule culture produces
A. Somaclonal variation
B. Gametoclonal variation
C. Hybrid plants
D. Cybrids
Answer: B
35. Callus culture mainly produces
A. Gametoclonal variation
B. Zygotic variation
C. Somaclonal variation
D. Meiotic variation
Answer: C
36. Which hormone increases genetic instability?
A. Cytokinins
B. Auxins at high concentration
C. Gibberellins
D. ABA
Answer: B
37. Somaclonal variation is especially valuable in
A. Seedless crops
B. Vegetatively propagated crops
C. Annual weeds
D. Algae
Answer: B
38. A major application of gametoclonal variation is
A. Micropropagation
B. Pure line development
C. Secondary metabolite production
D. Cryopreservation
Answer: B
39. Doubled haploids are genetically
A. Heterozygous
B. Homozygous
C. Aneuploid
D. Triploid
Answer: B
40. Somaclonal variation can improve
A. Yield
B. Quality
C. Stress tolerance
D. All of the above
Answer: D
41. In vitro stress screening is faster than
A. Molecular screening
B. Field screening
C. Biochemical analysis
D. Cytological analysis
Answer: B
42. Which crop shows Fusarium resistance through somaclonal variation?
A. Banana
B. Rice
C. Wheat
D. Barley
Answer: A
43. Gametoclonal variation mainly exploits
A. Mitosis
B. Meiosis
C. Somatic mutation
D. Polyploidy
Answer: B
44. Which is NOT an advantage of gametoclonal variation?
A. Rapid homozygosity
B. Expression of recessive traits
C. Genetic uniformity
D. High heterozygosity
Answer: D
45. Somaclonal variation is detected at which level?
A. Morphological
B. Biochemical
C. Molecular
D. All of the above
Answer: D
46. Variation due to culture conditions is called
A. Natural variation
B. Induced mutation
C. Culture-induced variation
D. Hybrid variation
Answer: C
47. Which crop is improved for drought tolerance using somaclonal variation?
A. Rice
B. Wheat
C. Maize
D. All of the above
Answer: D
48. Gametoclonal variation is less random because
A. It uses somatic cells
B. It involves haploid genomes
C. It avoids mutations
D. It avoids culture stress
Answer: B
49. The main disadvantage of both variations is
A. Lack of variation
B. Need for field testing
C. Low mutation rate
D. Poor regeneration
Answer: B
50. Somaclonal and gametoclonal variations are best used as
A. Replacement of breeding
B. Complementary tools in breeding
C. Only research tools
D. Tissue culture limitations
Answer: B

Comments

Popular Posts

❥ Southern Blotting Notes

Southern Blotting  ❥ π“†ž❥ π“†ž❥ π“†ž❥ π“†ž❥ π“†ž❥ π“†ž❥ π“†ž❥ π“†ž❥ π“†ž❥  Introduction Southern blotting is a molecular biology technique used for the detection of specific DNA sequences in a complex mixture of DNA. It was developed by Edwin M. Southern in 1975. The method involves restriction digestion of DNA, separation by gel electrophoresis, transfer (blotting) onto a membrane, and hybridization with a labeled DNA probe. Principle of Southern Blotting The technique is based on the principle of complementary base pairing. A single-stranded labeled DNA probe hybridizes specifically with its complementary DNA sequence immobilized on a membrane. Detection of the label confirms the presence and size of the target DNA fragment. Steps Involved in Southern Blotting. 1. Isolation of DNA Genomic DNA is extracted from cells or tissues. DNA must be pure and intact to ensure accurate results. 2. Restriction Enzyme  Digestion DNA is digested using specific restriction endonucleases. Produces DNA f...

AFLP--Amplified Fragment Length Polymorphism

AFLP is a PCR-based DNA fingerprinting technique combining restriction digestion and selective PCR amplification of genomic DNA fragments. Developed by Vos et al., 1995. AFLP detects DNA polymorphisms at the genomic level and is highly reproducible and sensitive. Used in genetic mapping, diversity studies, phylogenetics, and marker-assisted selection. Principle AFLP relies on restriction digestion of genomic DNA, followed by ligation of adaptors and PCR amplification of a subset of fragments. Polymorphism arises due to variations in restriction sites, fragment length, insertions, or deletions. Key idea: Restriction digestion → Adaptor ligation → Selective amplification → Gel separation → Detection of polymorphic bands Materials Required Genomic DNA Restriction enzymes (usually EcoRI and MseI) Adaptors complementary to restriction sites PCR reagents: Taq polymerase, dNTPs, buffer, Mg²⁺ Primers complementary to adaptors with selective nucleotides Thermal cycler Polyacrylamide or agarose ...

GEL RETARDATION ANALYSIS

GEL RETARDATION ANALYSIS (EMSA – Electrophoretic Mobility Shift Assay) Introduction Gel retardation analysis, also known as Electrophoretic Mobility Shift Assay (EMSA), is a widely used in vitro technique for studying DNA–protein and RNA–protein interactions. The method is based on the observation that a DNA–protein complex migrates more slowly than free DNA during non-denaturing gel electrophoresis, resulting in a mobility shift or “retardation”. EMSA is extensively used to study transcription factor binding, regulatory DNA elements, and binding specificity. Definition Gel retardation analysis (EMSA) is a technique used to detect and analyze binding interactions between nucleic acids and proteins by observing the reduced electrophoretic mobility of nucleic acid–protein complexes compared to free nucleic acids. Principle A labeled DNA or RNA probe is incubated with a specific binding protein. When binding occurs, a nucleic acid–protein complex is formed. This complex has a larger size ...

DNA-Mediated Gene Transfer – Detailed Notes

DNA-Mediated Gene Transfer – Detailed Notes 1. Definition DNA-mediated gene transfer refers to the direct introduction of exogenous DNA into a host cell’s genome or cytoplasm without using viral or bacterial vectors. It is a physical or chemical approach to achieve gene delivery. Also called direct gene transfer. 2 . Principle Foreign DNA is delivered into host cells through physical or chemical methods. DNA may integrate into the host genome (stable transformation) or remain episomal (transient expression). Expression depends on: DNA sequence and promoter Type of host cell Delivery efficiency 3. Types of DNA-Mediated Gene Transfer A. Physical Methods These methods use physical forces to introduce DNA into cells. Microinjection DNA is injected directly into the nucleus or cytoplasm using a glass micropipette. Used in: animal embryos, oocytes, plant protoplasts Advantages: Precise, can deliver large DNA fragments Limitations: Labor-intensive, requires specialized equipment, low throughp...

Agrobacterium & CaMV-Mediated Gene Transfer –

Agrobacterium and CaMV-Mediated Gene Transfer – Detailed Notes 1. Introduction Gene transfer in plants is often achieved by exploiting natural genetic mechanisms of Agrobacterium tumefaciens and Cauliflower Mosaic Virus (CaMV). These systems allow stable introduction of foreign genes into plant genomes for transgenic plant development. 2. Agrobacterium-Mediated Gene Transfer 2.1 Definition Agrobacterium-mediated gene transfer uses the natural ability of Agrobacterium tumefaciens, a soil bacterium, to transfer a part of its DNA (T-DNA) into plant cells. T-DNA integrates into the plant nuclear genome, enabling stable transformation. 2.2 Mechanism Recognition and attachment Agrobacterium detects phenolic compounds secreted by wounded plant cells. These compounds activate virulence (vir) genes on the Ti (tumor-inducing) plasmid. Activation of vir genes VirA (sensor kinase) and VirG (response regulator) induce expression of other vir genes (VirB, VirC, VirD, VirE). T-DNA processing and tran...

❥NORTHERN BLOTTING

NORTHERN BLOTTING – 30 MARK DETAILED NOTES  π“†ž❥ π“†ž❥ π“†ž❥ π“†ž❥ π“†ž❥ π“†ž ❥ π“†ž❥ π“†ž❥  Northern blotting is a molecular biology technique used to detect specific RNA molecules in a complex mixture. It provides information about gene expression, RNA size, and transcript abundance by hybridizing RNA with a labeled complementary DNA or RNA probe. πŸ“Œ Named by analogy to Southern blotting (DNA detection). 2. Principle The principle of Northern blotting is based on: Separation of RNA molecules by size using denaturing agarose gel electrophoresis Transfer (blotting) of separated RNA onto a nylon or nitrocellulose membrane Hybridization of membrane-bound RNA with a labeled complementary probe Detection of RNA–probe hybrids by autoradiography or chemiluminescence ✔ Only RNA sequences complementary to the probe will be detected. 3. Types of RNA Analyzed mRNA (most common) rRNA tRNA miRNA and siRNA (with modified protocols) 4. Requirements / Materials Total RNA or poly(A)+ RNA Denaturing agarose ...

❥ preservation for germplasm conservation. Cryopreservation of vegetative propagated and recalcitrant seed species.

preservation for germplasm conservation. Cryopreservation of vegetative propagated and recalcitrant seed species.  ❥ π“†ž❥ π“†ž❥ π“†ž❥ π“†ž❥ π“†ž❥ π“†ž❥ π“†ž❥ π“†ž❥ π“†ž❥ 1. Introduction Germplasm conservation is the systematic preservation of genetic resources for present and future use. Many economically important plants are vegetatively propagated (banana, potato, sugarcane, cassava) or produce recalcitrant seeds (cocoa, rubber, coconut), which cannot be conserved by conventional seed storage. Cryopreservation offers a safe, long-term and genetically stable method for conserving such germplasm by storing living tissues at –196°C in liquid nitrogen (LN). 2. Need for Preservation of Germplasm Prevention of genetic erosion Conservation of elite, endangered and rare species Backup of field and in-vitro collections Support to crop improvement and breeding Preservation of pathogen-free planting material Conservation of plants with non-orthodox seeds 3. Limitations of Conventional Storage Methods Seed B...

Protoplast culture covering isolation, fusion, somatic hybrid & cybrid production, preferential chromosome elimination, role in CMS, and genetic transformation.

  Protoplast culture covering isolation, fusion, somatic hybrid & cybrid production, preferential chromosome elimination, role in CMS, and genetic transformation. Protoplast Culture 1. Introduction A protoplast is a plant cell without a cell wall, surrounded only by the plasma membrane. Protoplast culture allows direct access to the plasma membrane and genome, making it a powerful tool for: Somatic hybridization Cybrid production Genetic transformation Cytoplasmic trait transfer (e.g., CMS) 2. Isolation of Protoplasts 2.1 Source of Protoplasts Young leaves (mesophyll cells) Callus tissue Cell suspension cultures Roots or hypocotyls Young, actively dividing tissues are preferred due to high viability. 2.2 Methods of Protoplast Isolation A. Mechanical Method Cell walls removed by cutting and plasmolysis Rarely used Causes low yield and high damage B. Enzymatic Method (Most Common) Cell wall digested using enzymes: Enzyme Function Cellulase Degrades cellulose Pectinase Degrades mi...

Secondary Databases (PROSITE, PRINTS, BLOCKS)

Secondary Databases (PROSITE, PRINTS, BLOCKS  Secondary Databases Introduction Biological databases are broadly classified into primary and secondary databases. Primary databases store raw experimental data (e.g., nucleotide or protein sequences), whereas secondary databases contain derived information obtained by analyzing primary sequence data. Secondary databases are mainly used to: Identify protein families Detect conserved motifs, patterns, and domains Predict protein function Study structure–function relationships Examples of secondary databases include PROSITE, PRINTS, BLOCKS, Pfam, etc. 1. PROSITE Database Definition PROSITE is a secondary database that documents protein domains, families, and functional sites in the form of patterns and profiles. Developed by Swiss Institute of Bioinformatics (SIB) Maintained along with UniProt Principle PROSITE is based on the idea that functionally important regions of proteins are conserved during evolution. These conserved regions can ...

Gene Transfer Technologies – Detailed Notes

Gene Transfer Technologies – Detailed Notes 1. Definition Gene transfer is the process of introducing foreign DNA or genes into the genome of a target organism or cell. It allows the expression of new traits, study of gene function, and production of therapeutic proteins. Also known as gene delivery or genetic transformation. 2. Principles of Gene Transfer Involves delivery of DNA or RNA into cells or organisms. DNA can be integrated into the host genome or remain episomal (non-integrated). The goal is stable or transient expression of the transferred gene. Key considerations: Vector – vehicle for carrying the gene Target cell – plant, animal, microbial, or human cells Delivery method – physical, chemical, or biological 3. Types of Gene Transfer Gene transfer can be broadly classified into: A. Natural Gene Transfer Occurs in nature between organisms: Transformation: Uptake of naked DNA by bacteria. Transduction: DNA transfer via viruses (bacteriophages). Conjugation: Transfer of plasmi...