UNIT ONE
Basic Genetics: A Starting Point

Glossary

 

ALLELES
Alternate forms or varieties of a gene. The alleles for a trait occupy the same locus or position on homologous chromosomes and thus govern the same trait. However, because they are different, their action may result in different expressions of that trait.

AMINO ACIDS
Organic molecules that are building block of proteins. There are 20 different kinds of amino acids in living things. Proteins are composed of different combinations of amino acids assembled in chain-like molecules. Amino acids are primarily composed of carbon, oxygen, hydrogen, and nitrogen.

ANALOGUES are likenesses found in humans and animals.

CHROMOSOMES
Thread-like, gene-carrying bodies in the cell nucleus. Chromosomes are composed primarily of DNA and protein. They are visible only under magnification during certain stages of cell division. Humans have 46 chromosomes in each somatic cell and 23 in each sex cell.

COLLECTIVELY means altogether

.DIPLOID NUMBER
Referring to the full component of chromosomes normally found in somatic cells. In humans, the number is 46. See haploid number.

DNA (DEOXYRIBONUCLEIC ACID )
A large organic molecule that stores the genetic code for the synthesis of proteins. DNA is composed of sugars, phosphates and bases arranged in a double helix shaped molecular structure. Segments of DNA in chromosomes correspond to specific genes.

DOMINANT ALLELE
An allele that masks the presence of a recessive allele.


DOUBLE HELIX
The twisted ladder shape that is characteristic of DNA molecules.

ETHICAL is a principle of right or wrong or good conduct.

FERTILIZATION
Conception; the process of sexual reproduction by which the chromosomes from a sperm cell enter the nucleus of an ovum and combine with its chromosomes.

GAMETES
Reproductive cells--sperm or unfertilized ovum cells produced in the testes and ovaries of animals. Gametes are produced by meiosis. They normally have half the number of chromosomes found in somatic cells.

GENES
Units of inheritance usually occurring at specific locations, or loci, on a chromosome. Physically, a gene is a sequence of DNA bases that specify the order of amino acids in an entire protein or, in some cases, a portion of a protein. A gene may be made up of hundreds of thousands of DNA bases. Genes are responsible for hereditary characteristics in plants and animals.

GENETIC CODING refers to the genetic make-up of humans and other species.

GENOME is the human gene make-up.

GENOTYPE
The genetic makeup of an individual. Genotype can refer to an organism's entire genetic makeup or the alleles at a particular locus. See phenotype.

HAPLOID NUMBER
Referring to the number of chromosomes in gametes. Human sperm and ova normally contain only 23 chromosomes, which is the result of the halving of chromosome pairs in meiosis. See diploid number.

HEMOPHILIA
An X-linked genetically inherited recessive disease in which one or more of the normal blood clotting factors is not produced. This results in prolonged bleeding from even minor cuts and injuries. Hemophilia most often afflicts males.

HETEROZYGOUS
A genotype consisting of two different alleles of a gene for a particular trait (Aa). Individuals who are heterozygous for a trait are referred to as heterozygotes. See homozygous.

HOMOLOGOUS CHROMOSOMES
Chromosomes that are paired during meiosis. Such chromosomes are alike with regard to size and also position of the centromere. They also have the same genes, but not necessarily the same alleles, at the same locus or location.

HOMOZYGOUS
Having the same allele at the same locus on both members of a pair of homologous chromosomes. Homozygous also refers to a genotype consisting of two identical alleles of a gene for a particular trait. An individual may be homozygous dominant (AA) or homozygous recessive (aa). Individuals who are homozygous for a trait are referred to as homozygotes. See heterozygous.

HUNTINGTON'S DISEASE
A severe genetically inherited fatal degenerative nerve disorder. The symptoms usually do not appear until early middle age. There is a progressive loss of muscle control that inevitably leads to paralysis and death.

INDIVIDUALLY means each person.

INDIVIDUATION is the distinctiveness or uniqueness of an individual.

INTERRELATEDNESS is to come into mutual relationship.

LIVING SPECIES are animals other than humans.

MEIOSIS
Cell division in specialized tissues of ovaries and testes which results in the production of sperm or ova. Meiosis involves two divisions and results in four daughter cells, each containing only half the original number of chromosomes--23 in the case of humans. These cells can develop into gametes. See mitosis

MITOSIS
The simple cell division process that occurs in somatic cells. One cell divides into two offspring cells that are identical to each other in their chromosome complement. Mitosis produces cells with diploid numbers of chromosomes--46 in the case of humans. See meiosis.

MORAL means the judgment of the goodness or badness of human actions.

MUTATION
An alteration of genetic material such that a new variation is produced. For instance, a trait that has only one allele (A) can mutate to a new form (a). This is the only mechanism of evolution that can produce new alleles of a gene. Technically, mutation refers to changes in DNA bases as well as changes in chromosome number and /or structure.

NUCLEIC ACIDS
The largest type of molecule in living organisms. It is composed of a chain of nucleotides that code for the synthesis of specific proteins. DNA and RNA are types of nucleic acid.

NUCLEOTIDE
The basic building block of nucleic acid. It consists of any one of four specific purine or pyrimidine bases attached to a ribose or deoxyribose sugar and phosphate group.

OVUM (PLURAL OVA )
A female sex cell or gamete.

PHENOTYPE
The observable or detectable characteristics of an individual organism; the detectable expression of a genotype.

POLYMORPHISM
A genetic trait controlled by more than one allele, each of which has a frequency of 1% or greater in the population gene pool. See balanced polymorphism.
population a1 more or less distinct group of individuals within a species who tend to restrict their mate selection to members of their group. Members of a population tend to have similar genetic characteristics due to generations of interbreeding.

PROTEINS
Any of a large number of complex organic molecules that are composed of one or more chains of amino acids. Proteins can serve a wide variety of functions through their ability to bind to other molecules. Proteins may be enzymes, hormones, antibodies, structural components, or gas-transporting molecules.

RECESSIVE ALLELE
An allele that is masked in the phenotype by the presence of a dominant allele. Recessive alleles are expressed in the phenotype when the genotype is homozygous recessive (aa).

RECOMBINATION
The exchange of genetic material between homologous chromosomes at the beginning of meiosis. This results in sperm and ova with greater genetic diversity. Specifically, a portion of a chromosome is broken and reattached on another chromosome. Recombination is also referred to as crossing-over.

RETINAL ATROPHY concerns the wasting away of the inner lining of the eye.RNA

(RIBONUCLEIC ACID )A type of nucleic acid that is found in both the nucleus and the cytoplasm of cells. Unlike DNA, RNA is single stranded. Messenger RNA (mRNA) carries the genetic code from the DNA in the chromosomes and translates it with the help of transfer RNA (tRNA) at the site of the ribosomes in the cytoplasm in order to assemble, or synthesize, proteins.

SEX CELL
A gamete, either a sperm or an ovum. Sex cells are produced by the meiosis process. See somatic cell.

SEX-LINKED
Referring to a gene that is part of a sex chromosome. Since all of the genes on a chromosome are inherited as a package, they are essentially linked together.

SICKLE-CELL TRAIT
A genetically inherited recessive condition in which red blood cells are distorted resulting in severe anemia and related symptoms that are often fatal in childhood.
SOLIDARITY is a togetherness or unity.

SOMATIC CELL
Basically, all the cells in the body except those directly involved with reproduction. Most cells in multicellular plants and animals are somatic cells. They reproduce by mitosis and have a diploid number of chromosomes. See sex cell.

SPECIES
The largest natural population of organisms that can interbreed to produce fertile offspring. Members of one species are reproductively isolated from members of all other species (i.e., they cannot mate with them to produce fertile offspring).

SPERM
A male sex cell or gamete.

TAY-SACHS DISEASE
An inherited metabolic abnormality that is fatal in early childhood. Eastern European Jews have an unusually high frequency of this harmful recessive allele in their population. However, it can occur in any human group.

TRANSGENIC is moving of genes.

X-LINKED
Referring to a gene that is carried by an X chromosome. See sex-linked gene.

ZYGOTE
A "fertilized" ovum. More precisely, this is a cell that is formed when a sperm and an ovum combine their chromosomes at conception. A zygote contains the full complement of chromosomes (in humans 46) and has the potential of developing into an entire organism.Sources include: Synthetic Theory of Evolution: Glossary of Terms by Dennis O’Neil http://anthro.palomar.edu/glossary.htm#somatic_cell

 

 

 

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