Glossary of Scientific Terms
A - B
- C - D - E
- F - G - H
- I - J - K - L
- M - N - O
- P - Q - R
- S - T - U
- V - W - X - Y - Z
R
Recessive trait
The quality of a gene or allele regarding its ability to express a phenotype.
A recessive allele can only express its phenotype if both copies in a
diploid organisms are identical. Often, a recessive allele is matched
with a dominant allele, which overrides the activity of the recessive
one. In this case, the effect of the gene cannot be seen, but it can still
be inherited. These are important considerations in genetic diseases that
are often caused by defective copies of a gene (allele) that cause the
disease only, if both copies of the gene are defective (homozygous for
the recessive allele). Heterozygous individuals with a healthy allele
do not suffer the disease but are carriers. Examples of recessive genetic
diseases are cystic fibrosis and hypercholesterolemia.
Redundancy
Reduncancy in biology is an important hallmark of the complexity and robustness
of life. Redundancy usually means that different parts of a cell or organism
can carry out the same function. This way, a defective part is not damaging
to the cell. Redundancy also allows evolution of diversity, because a
particular structure may mutate (change) and adopt a new function. The
loss of the old function is taken over by another part of the cell or
organism.
Replication, of DNA
The replication of DNA is a fundamental process during cell division that
provides the two daughter cells (offspring) with identical sets of genes.
The replication requires the temporary separation of the DNA double helix
into single strand forms where each of the two strands serves as a molecular
template for the synthesis of one new complementary strand to form two
new double helical copies of the original DNA. The accuracy of replication
is based on the specific molecular interaction between two of the four
existing nucleotides (A adenine; T thymine; G guanine; C cytosine) to
form only AT or GC base pairs. Any other pairing can cause mutations in
the daughter DNA, a process that occurs very rarely, and is one of the
processes leading to genetic diversity of life.
Ribosome
The cellular particles made of protein and RNA subunits that catalyze
the synthesis of proteins along a messenger RNA (mRNA) template. This
process is called translation that converts a nucleic acid genetic code
into an amino acid sequence. The result are proteins (enzymes) with each
having a specific structure and function carrying out a particular metabolic
reaction in a cell.
RNA
Ribonucleic acid, the most common form of nucleic acid used for storage
of chemical energy, processing genetic information from genes (DNA) via
messenger RNA (mRNA) into proteins. RNA is one of the most ancient form
of molecular structures with enzymatic activity. As a matter of fact, protein
biosynthesis is entirely controlled by RNA molecules including mRNA (genetic
information), transfer RNA (tRNA) for translating the DNA code into amino
acid code, and ribosomal RNA (rRNA) that provide the enzymatic linkage
(chemical bond formation) of amino acids into proteins. The use of RNA
probably precedes the use of proteins and most modern genomes (except for
some viruses) are made of DNA instead of RNA but can only be read by proteins.
DNA is the more chemically stable of the two forms of nucleic acids.
H
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Copyright © 2000-2006 Lukas
K. Buehler
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