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2011 plant tissue culture using totipotancy

Plant tissue culture involves growing plant cells, tissues or organs in sterile conditions on nutrient media. Key factors include the growth media, environmental conditions, and the explant source tissue. Plant cells have the abilities of totipotency, dedifferentiation, and competency. Tissue culture is used for micropropagation, genetic modification, pathogen elimination, and more. Common types include callus, organ, and embryo culture. Somatic embryogenesis and organogenesis allow regeneration of whole plants. Tissue culture can generate somaclonal variation through genetic or epigenetic changes.

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Plant Tissue Culture The culture and maintenance of plant cells and organs The culture of plant seeds, organs, tissues, cells, or protoplasts on nutrient media under sterile conditions The growth and development of plant seeds, organs, tissues, cells or protoplasts on nutrient media under sterile (axenic) conditions The in vitro, aseptic plant culture for any purpose including genetic transformation and other plant breeding objectives, secondary product production, pathogen elimination or for asexual (micropropagation) or sexual propagation
Important Factors • Growth Media – Minerals, Growth factors, Carbon source, Hormones • Environmental Factors – Light, Temperature, Photoperiod, Sterility • Explant Source – Usually, the younger, less differentiated , the better for tissue culture – Different species show differences in amenability to tissue culture – In many cases, different genotypes within a species will have variable responses to tissue culture
Basis for Plant Tissue Culture • Two hormones affect plant differentiation: – Auxin: Stimulates root development – Cytokinin: Stimulates Shoot Development • Generally, the ratio of these two hormones can determine plant development: –  Auxin ↓Cytokinin = Root Development –  Cytokinin ↓Auxin = Shoot Development – Auxin = Cytokinin = Callus Development
Control of in vitro culture Cytokinin Auxin Leaf strip Adventitious Shoot Root Callus
1. Environmental condition optimized (nutrition, light, temperature). 2. Ability to give rise to callus, embryos, adventitious roots and shoots. 3. Ability to grow as single cells (protoplasts, microspores, suspension cultures). 4. Plant cells are totipotent, able to regenerate a whole plant. Characteristic of Plant Tissue Culture Techniques
Three Fundamental Abilities of Plants  Totipotency The potential or inherent capacity of a plant cell to develop into an entire plant if suitably stimulated. It implies that all the information necessary for growth and reproduction of the organism is contained in the cell  Dedifferentiation Capacity of mature cells to return to meristematic condition and development of a new growing point, follow by redifferentiation which is the ability to reorganize into new organ  Competency The endogenous potential of a given cells or tissue to develop in a particular way
Why is tissue culture important? Plant tissue culture has value in studies such as cell biology, genetics, biochemistry, and many other research areas Crop Improvement Seed Production – Plant Propagation Technique Genetic material conservation
Types of In Vitro Culture (explant based)  Culture of intact plants (seed and seedling culture)  Embryo culture (immature embryo culture)  Organ culture  Callus culture  Cell suspension culture  Protoplast culture
Tissue Culture Applications Micropropagation Germplasm preservation Somaclonal variation Haploid & dihaploid production In vitro hybridization – protoplast fusion Plant genetic engineering
Seed culture Use:  Increasing efficiency of germination of seeds that are difficult to germinate in vivo  Precocious germination by application of plant growth regulators  Production of clean seedlings for explants or meristem culture  In vitro selection Growing seed aseptically in vitro on artificial media
Embryo culture Use:  Rescue embryos (embryo rescue) from wide crosses where fertilization occurred, but embryo development did not occur  Production of plants from embryos developed by non-sexual methods (haploid production)  Overcoming embryo abortion due to incompatibility barriers  Overcoming seed dormancy and self- sterility of seeds  Shortening of breeding cycle Growing embryo aseptically in vitro on artificial nutrient media
Organ culture Any plant organ can serve as an explant to initiate cultures No. Organ Culture types 1. Shoot Shoot tip culture 2. Root Root culture 3. Leaf Leaf culture 4. Flower Anther/ovary culture
Shoot apical meristem culture  Production of virus free germplasm  Mass production of desirable genotypes  Facilitation of exchange between locations (production of clean material)  Cryopreservation (cold storage) or in vitro conservation of germplasm
Root organ culture  Production secondary metabolites  Study the physiology and metabolism of roots, and primary root determinate growth patterns
Ovary or ovule culture  Production of haploid plants  A common explant for the initiation of somatic embryogenic cultures  Overcoming abortion of embryos of wide hybrids at very early stages of development due to incompatibility barriers  In vitro fertilization for the production of distant hybrids avoiding style and stigmatic incompatibility that inhibits pollen germination and pollen tube growth
Anther and microspore culture  Production of haploid plants  Production of homozygous diploid lines through chromosome doubling, thus reducing the time required to produce inbred lines  Uncovering mutations or recessive phenotypes
Callus Culture Callus: An un-organised mass of cells A tissue that develops in response to injury caused by physical or chemical means Most cells of which are differentiated although may be and are often highly unorganized within the tissue
Cell suspension culture  When callus pieces are agitated in a liquid medium, they tend to break up.  Suspensions are much easier to bulk up than callus since there is no manual transfer or solid support.
Introduction into suspension + Plate out Sieve out lumps 1 2 Pick off growing high producers Initial high density Subculture and sieving
Protoplast The living material of a plant or bacterial cell, including the protoplasm and plasma membrane after the cell wall has been removed.
Somatic Hybridization Development of hybrid plants through the fusion of somatic protoplasts of two different plant species/varieties
Somatic hybridization technique 1. isolation of protoplast 2. Fusion of the protoplasts of desired species/varieties 3. Identification and Selection of somatic hybrid cells 4. Culture of the hybrid cells 5. Regeneration of hybrid plants
Uses for Protoplast Fusion  Combine two complete genomes – Another way to create allopolyploids  In vitro fertilization  Partial genome transfer – Exchange single or few traits between species – May or may not require ionizing radiation  Genetic engineering – Micro-injection, electroporation, Agrobacterium  Transfer of organelles – Unique to protoplast fusion – The transfer of mitochondria and/or chloroplasts between species
Plant Regeneration Pathways  Organogenesis Relies on the production of organs either directly from an explant or callus structure  Somatic Embryogenesis Embryo-like structures which can develop into whole plants in a way that is similar to zygotic embryos are formed from somatic cells  Existing Meristems (Microcutting) Uses meristematic cells to regenerate whole plant. (Source:Victor. et al., 2004)
Organogenesis • The ability of non- meristematic plant tissues to form various organs de novo. • The formation of adventitious organs • The production of roots, shoots or leaves • These organs may arise out of pre-existing meristems or out of differentiated cells • This may involve a callus intermediate but often occurs without callus.
Indirect organogenesis Explant → Callus → Meristemoid → Primordium • Dedifferentiation – Less committed, – More plastic developmental state • Induction – Cells become organogenically competent and fully determined for primordia production • Differentiation
Direct Organogenesis Direct shoot/root formation from the explant
Somatic Embryogenesis • The formation of adventitious embryos • The production of embryos from somatic or “non-germ” cells. • It usually involves a callus intermediate stage which can result in variation among seedlings
Two routes to somatic embryogenesis (Sharp et al., 1980) • Direct embryogenesis – Embryos initiate directly from explant in the absence of callus formation. • Indirect embryogenesis – Callus from explant takes place from which embryos are developed.
Direct somatic embryogenesis Direct embryo formation from an explant
Indirect Somatic Embryogenesis Explant → Callus Embryogenic → Maturation → Germination 1. Calus induction 2. Callus embryogenic development 3. Maturation 4. Germination
Development  Auxin must be removed for embryo development  Continued use of auxin inhibits embryogenesis  Stages are similar to those of zygotic embryogenesis – Globular – Heart – Torpedo – Cotyledonary – Germination (conversion)
Various terms for non-zygotic embryos  Adventious embryos Somatic embryos arising directly from other organs or embryos.  Parthenogenetic embryos (apomixis) Somatic embryos are formed by the unfertilized egg.  Androgenetic embryos Somatic embryos are formed by the male gametophyte.
Somatic embryogenesis as a means of propagation is seldom used  High probability of mutations  The method is usually rather difficult.  Losing regenerative capacity become greater with repeated subculture  Induction of embryogenesis is very difficult with many plant species.  A deep dormancy often occurs with somatic embryogenesis
Somatic Embryogenesis and Organogenesis • Both of these technologies can be used as methods of micropropagation. • It is not always desirable because they may not always result in populations of identical plants. • The most beneficial use of somatic embryogenesis and organogenesis is in the production of whole plants from a single cell (or a few cells).
Somatic embryogenesis differs from organogenesis • Bipolar structure with a closed radicular end rather than a monopolar structure. • The embryo arises from a single cell and has no vascular connection with the mother tissue.
Peanut somatic embryogenesis
Microcutting propagation • It involves the production of shoots from pre-existing meristems only. • Requires breaking apical dominance • This is a specialized form of organogenesis
Steps of Micropropagation • Stage 0 – Selection & preparation of the mother plant – sterilization of the plant tissue takes place • Stage I - Initiation of culture – explant placed into growth media • Stage II - Multiplication – explant transferred to shoot media; shoots can be constantly divided • Stage III - Rooting – explant transferred to root media • Stage IV - Transfer to soil – explant returned to soil; hardened off
Somaclonal Variation  Variation found in somatic cells dividing mitotically in culture  A general phenomenon of all plant regeneration systems that involve a callus phase Some mechanisms:  Karyotipic alteration  Sequence variation  Variation in DNA methylation Two general types of somaclonal variation:  Heritable, genetic changes (alter the DNA)  Stable, but non-heritable changes (alter gene expression, epigenetic)
Epigenetic the gene regulation that does not involve making changes to the SEQUENCE of the DNA, but rather to the actual BASES within the nucleotides and to the HISTONES The three main mechanisms for regulation:  CpG island methylation (…meCGmeCGmeCGmeCGmeCGmeCGmeCG…)  acetylation and methylation of histone H3  the production of antisense RNA