Plant chromosomes

When mitosis is blocked by colchicine, the treated cells may be left with an extra set of chromosomes. Plants with extra sets of chromosomes are typically larger and more vigorous than normal plants. Flowers developed in this way may grow with double the normal number of petals, and fruits may produce much larger amounts of sugar. 

Dubcovsky J., Ramakrishna W., SanMiguel P.J., Busso C.S., Yan L., ShiloflfB.A., Ben-netzen J.L. (2001). Comparative sequence analysis of collinear barley and rice bacterial artificial chromosomes. Plant Physiol. 125 1342-1353. 

Colchiciae (23) is a toxic substance occurring ia Colchicum autumnale, it coataias the aucleus of pyrogaUol trimethyl ether. Colchiciae has beea used ia the treatmeat of acute gout, and ia plant genetics research to effect doubling of chromosomes. 

Plant and animal cells have numerous chromosomes. Growth rates are relatively slow. A typical nutrient medium will contain a large number of vitamins and growth factors in addition to complex nitrogen sources, because other specialized cells in the original structures supply these needs. A plant or animal cell is not hke a microbial cell in its ability to function independently. 

Chromosomal organization, DNA replication, transcription, ribosome synthesis, and mitosis in plant cells are grossly similar to the analogous features in animals. 

In terms of evolutionary biology, the complex mitotic process of higher animals and plants has evolved through a progression of steps from simple prokaryotic fission sequences. In prokaryotic cells, the two copies of replicated chromosomes become attached to specialized regions of the cell membrane and are separated by the slow intrusion of the membrane between them. In many primitive eukaryotes, the nuclear membrane participates in a similar process and remains intact the spindle microtubules are extranuclear but may indent the nuclear membrane to form parallel channels. In yeasts and diatoms, the nuclear membrane also remains intact, an intranuclear polar spindle forms and attaches at each pole to the nuclear envelope, and a single kinetochore microtubule moves each chromosome to a pole. In the cells of higher animals and plants, the mitotic spindle starts to form outside of the nucleus, the nuclear envelope breaks down, and the spindle microtubules are captured by chromosomes (Kubai, 1975 Heath, 1980 Alberts et al., 1989). 

Several groups of drugs that bind to tubulin at different sites interfere with its polymerization into microtubules. These drugs are of experimental and clinical importance (Bershadsky and Vasiliev, 1988). For example, colchicine, an alkaloid derived from the meadow saffron plant Colchicum autumnale or Colchicum speciosum), is the oldest and most widely studied of these drugs. It forms a molecular complex with tubulin in the cytosol pool and prevents its polymerization into microtubules. Other substances such as colcemid, podophyllotoxin, and noco-dazole bind to the tubulin molecule at the same site as colchicine and produce a similar effect, albeit with some kinetic differences. Mature ciliary microtubules are resistant to colchicine, whereas those of the mitotic spindle are very sensitive. Colchicine and colcemid block cell division in metaphase and are widely used in cytogenetic studies of cultured cells to enhance the yield of metaphase plate chromosomes. 

We are concerned here with systems that have been studied using secondary products—flavonoids and terpenoids in particular— but other information, including micro- and macrofossils, and occasionally chromosome numbers, will be included in the discussions when snch information is available. The majority of current research on postglacial reestablishment of plant distribution patterns is based on DNA seqnence information. In a few instances below, reference will be made to such information, but this in not the place for a detailed review of that literature. 

The chromatid separation process has also remained mysterious. It is an autonomous process that does not direcdy depend on the mitotic spindle (Wilson 1925, Mazia 1961). This is most vividly seen in cells whose spindles have been destroyed by spindle poisons such as colchicine. In many organisms, in particular in plant cells, the cell cycle delay induced by colchicine is only transient and chromatids eventually split apart in the complete absence of a mitotic spindle (Mole-Bajer 1958, Rieder Palazzo 1992) (Fig. 2). Mitosis in the presence of colchicine or colcemid (known as c-mitosis) leads to the production of daughter cells with twice the normal complement of chromosomes. This process is routinely used for manipulating plant genomes and may contribute to the therapeutic effects of taxol in treating breast cancer. 

A1-Hakkak ZSH, Hamamy HA, Murad AMB, et al. 1986. Chromosome aberrations in workers at a storage battery plant in Iraq. MutRes 171 53-60. 

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