StemCell Therapy

The chromosome set of a species remains relatively stable over long periods of time. However, within populations there can be found abnormalities involving the structure or number of chromosomes. These alterations arise spontaneously from errors in the normal processes of the cell. Their consequences are usually deleterious, giving rise to individuals who are unhealthy or sterile, though in rare cases alterations provide new adaptive opportunities that allow evolutionary change to occur. In fact, the discovery of visible chromosomal differences between species has given rise to the belief that radical restructuring of chromosome architecture has been an important force in evolution.

Two important principles dictate the properties of a large proportion of structural chromosomal changes. The first principle is that any deviation from the normal ratio of genetic material in the genome results in genetic imbalance and abnormal function. In the normal nuclei of both diploid and haploid cells, the ratio of the individual chromosomes to one another is 1:1. Any deviation from this ratio by addition or subtraction of either whole chromosomes or parts of chromosomes results in genomic imbalance. The second principle is that homologous chromosomes go to great lengths to pair at meiosis. The tightly paired homologous regions are joined by a ladderlike longitudinal structure called the synaptonemal complex. Homologous regions seem to be able to find each other and form a synaptonemal complex whether or not they are part of normal chromosomes. Therefore, when structural changes occur, not only are the resulting pairing formations highly characteristic of that type of structural change but they also dictate the packaging of normal and abnormal chromosomes into the gametes and subsequently into the progeny.

The simplest, but perhaps most damaging, structural change is a deletionthe complete loss of a part of one chromosome. In a haploid cell this is lethal, because part of the essential genome is lost. However, even in diploid cells deletions are generally lethal or have other serious consequences. In a diploid a heterozygous deletion results in a cell that has one normal chromosome set and another set that contains a truncated chromosome. Such cells show genomic imbalance, which increases in severity with the size of the deletion. Another potential source of damage is that any recessive, deleterious, or lethal alleles that are in the normal counterpart of the deleted region will be expressed in the phenotype. In humans, cri-du-chat syndrome is caused by a heterozygous deletion at the tip of the short arm of chromosome 5. Infants are born with this condition as the result of a deletion arising in parental germinal tissues or even in sex cells. The manifestations of this deletion, in addition to the cat cry that gives the syndrome its name, include severe intellectual disability and an abnormally small head.

A heterozygous duplication (an extra copy of some chromosome region) also results in a genomic imbalance with deleterious consequences. Small duplications within a gene can arise spontaneously. Larger duplications can be caused by crossovers following asymmetrical chromosome pairing or by meiotic irregularities resulting from other types of altered chromosome structures. If a duplication becomes homozygous, it can provide the organism with an opportunity to acquire new genetic functions through mutations within the duplicate copy.

An inversion occurs when a chromosome breaks in two places and the region between the break rotates 180 before rejoining with the two end fragments. If the inverted segment contains the centromere (i.e., the point where the two chromatids are joined), the inversion is said to be pericentric; if not, it is called paracentric. Inversions do not result in a gain or loss of genetic material, and they have deleterious effects only if one of the chromosomal breaks occurs within an essential gene or if the function of a gene is altered by its relocation to a new chromosomal neighbourhood (called the position effect). However, individuals who are heterozygous for inversions produce aberrant meiotic products along with normal products. The only way uninverted and inverted segments can pair is by forming an inversion loop. If no crossovers occur in the loop, half of the gametes will be normal and the other half will contain an inverted chromosome. If a crossover does occur within the loop of a paracentric inversion, a chromosome bridge and an acentric chromosome (i.e., a chromosome without a centromere) will be formed, and this will give rise to abnormal meiotic products carrying deletions, which are inviable. In a pericentric inversion, a crossover within the loop does not result in a bridge or an acentric chromosome, but inviable products are produced carrying a duplication and a deletion.

If a chromosome break occurs in each of two nonhomologous chromosomes and the two breaks rejoin in a new arrangement, the new segment is called a translocation. A cell bearing a heterozygous translocation has a full set of genes and will be viable unless one of the breaks causes damage within a gene or if there is a position effect on gene function. However, once again the pairing properties of the chromosomes at meiosis result in aberrant meiotic products. Specifically, half of the products are deleted for one of the chromosome regions that changed positions and half of the products are duplicated for the other. These duplications and deletions usually result in inviability, so translocation heterozygotes are generally semisterile (half-sterile).

Two types of changes in chromosome numbers can be distinguished: a change in the number of whole chromosome sets (polyploidy) and a change in chromosomes within a set (aneuploidy).

An individual with additional chromosome sets is called a polyploid. Individuals with three sets of chromosomes (triploids, 3n) or four sets of chromosomes (tetraploids, 4n) are polyploid derivatives of the basic diploid (2n) constitution. Polyploids with odd numbers of sets (e.g., triploids) are sterile, because homologous chromosomes pair only two by two, and the extra chromosome moves randomly to a cell pole, resulting in highly unbalanced, nonfunctional meiotic products. It is for this reason that triploid watermelons are seedless. However, polyploids with even numbers of chromosome sets can be fertile if orderly two-by-two chromosome pairing occurs.

Though two organisms from closely related species frequently hybridize, the chromosomes of the fusing partners are different enough that the two sets do not pair at meiosis, resulting in sterile offspring. However, if by chance the number of chromosome sets in the hybrid accidentally duplicates, a pairing partner for each chromosome will be produced, and the hybrid will be fertile. These chromosomally doubled hybrids are called allotetraploids. Bread wheat, which is hexaploid (6n) due to several natural spontaneous hybridizations, is an example of an allotetraploid. Some polyploid plants are able to produce seeds through an asexual type of reproduction called apomixis; in such cases, all progeny are identical to the parent. Polyploidy does arise spontaneously in humans, but all polyploids either abort in utero or die shortly after birth.

Some cells have an abnormal number of chromosomes that is not a whole multiple of the haploid number. This condition is called aneuploidy. Most aneuploids arise by nondisjunction, a failure of homologous chromosomes to separate at meiosis. When a gamete of this type is fertilized by a normal gamete, the zygotes formed will have an unequal distribution of chromosomes. Such genomic imbalance results in severe abnormalities or death. Only aneuploids involving small chromosomes tend to survive and even then only with an aberrant phenotype.

The most common form of aneuploidy in humans results in Down syndrome, a suite of specific disorders in individuals possessing an extra chromosome 21 (trisomy 21). The symptoms of Down syndrome include intellectual disability, severe disorders of internal organs such as the heart and kidneys, up-slanted eyes, an enlarged tongue, and abnormal dermal ridge patterns on the fingers, palms, and soles. Other forms of aneuploidy in humans result from abnormal numbers of sex chromosomes. Turner syndrome is a condition in which females have only one X chromosome. Symptoms may include short stature, webbed neck, kidney or heart malformations, underdeveloped sex characteristics, or sterility. Klinefelter syndrome is a condition in which males have one extra female sex chromosome, resulting in an XXY pattern. (Other, less frequent, chromosomal patterns include XXXY, XXXXY, XXYY, and XXXYY.) Symptoms of Klinefelter syndrome may include sterility, a tall physique, lack of secondary sex characteristics, breast development, and learning disabilities.

The data accumulated by scientists of the early 20th century provided compelling evidence that chromosomes are the carriers of genes. But the nature of the genes themselves remained a mystery, as did the mechanism by which they exert their influence. Molecular geneticsthe study of the structure and function of genes at the molecular levelprovided answers to these fundamental questions.

In 1869 Swiss chemist Johann Friedrich Miescher extracted a substance containing nitrogen and phosphorus from cell nuclei. The substance was originally called nuclein, but it is now known as deoxyribonucleic acid, or DNA. DNA is the chemical component of the chromosomes that is chiefly responsible for their staining properties in microscopic preparations. Since the chromosomes of eukaryotes contain a variety of proteins in addition to DNA, the question naturally arose whether the nucleic acids or the proteins, or both together, were the carriers of the genetic information. Until the early 1950s most biologists were inclined to believe that the proteins were the chief carriers of heredity. Nucleic acids contain only four different unitary building blocks, but proteins are made up of 20 different amino acids. Proteins therefore appeared to have a greater diversity of structure, and the diversity of the genes seemed at first likely to rest on the diversity of the proteins.

Evidence that DNA acts as the carrier of the genetic information was first firmly demonstrated by exquisitely simple microbiological studies. In 1928 English bacteriologist Frederick Griffith was studying two strains of the bacterium Streptococcus pneumoniae; one strain was lethal to mice (virulent) and the other was harmless (avirulent). Griffith found that mice inoculated with either the heat-killed virulent bacteria or the living avirulent bacteria remained free of infection, but mice inoculated with a mixture of both became infected and died. It seemed as if some chemical transforming principle had transferred from the dead virulent cells into the avirulent cells and changed them. In 1944 American bacteriologist Oswald T. Avery and his coworkers found that the transforming factor was DNA. Avery and his research team obtained mixtures from heat-killed virulent bacteria and inactivated either the proteins, polysaccharides (sugar subunits), lipids, DNA, or RNA (ribonucleic acid, a close chemical relative of DNA) and added each type of preparation individually to avirulent cells. The only molecular class whose inactivation prevented transformation to virulence was DNA. Therefore, it seemed that DNA, because it could transform, must be the hereditary material.

A similar conclusion was reached from the study of bacteriophages, viruses that attack and kill bacterial cells. From a host cell infected by one bacteriophage, hundreds of bacteriophage progeny are produced. In 1952 American biologists Alfred D. Hershey and Martha Chase prepared two populations of bacteriophage particles. In one population, the outer protein coat of the bacteriophage was labeled with a radioactive isotope; in the other, the DNA was labeled. After allowing both populations to attack bacteria, Hershey and Chase found that only when DNA was labeled did the progeny bacteriophage contain radioactivity. Therefore, they concluded that DNA is injected into the bacterial cell, where it directs the synthesis of numerous complete bacteriophages at the expense of the host. In other words, in bacteriophages DNA is the hereditary material responsible for the fundamental characteristics of the virus.

Today the genetic makeup of most organisms can be transformed using externally applied DNA, in a manner similar to that used by Avery for bacteria. Transforming DNA is able to pass through cellular and nuclear membranes and then integrate into the chromosomal DNA of the recipient cell. Furthermore, using modern DNA technology, it is possible to isolate the section of chromosomal DNA that constitutes an individual gene, manipulate its structure, and reintroduce it into a cell to cause changes that show beyond doubt that the DNA is responsible for a large part of the overall characteristics of an organism. For reasons such as these, it is now accepted that, in all living organisms, with the exception of some viruses, genes are composed of DNA.

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Heredity - Chromosomal aberrations | Britannica.com

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