KEY TERMS:
- A homomultimer is a protein composed of identical subunits.
- A heteromultimer is a protein that is composed of nonidentical subunits (coded by different genes).
- The one gene : one enzyme hypothesis summarizes the basis of modern genetics: that a gene is a stretch of DNA coding for a single polypeptide chain.
- Most mutations damage gene function.
The first systematic attempt to associate genes with enzymes
showed that each stage in a metabolic pathway is catalyzed by a single enzyme
and can be blocked by mutation in a different gene. This led to the one gene
: one enzyme hypothesis. Each metabolic step is catalyzed by a particular
enzyme, whose production is the responsibility of a single gene. A mutation in
the gene alters the activity of the protein for which it is responsible.
A modification in the hypothesis is needed to accommodate
proteins that consist of more than one subunit. If the subunits are all the
same, the protein is a homomultimer, represented by
a single gene. If the subunits are different, the protein is a heteromultimer. Stated as a more general rule applicable
to any heteromultimeric protein, the one gene : one enzyme hypothesis becomes
more precisely expressed as one gene : one polypeptide chain.
Identifying which protein represents a particular gene can
be a protracted task. The mutation responsible for creating Mendel's
wrinkled-pea mutant was identified only in 1990 as an alteration that
inactivates the gene for a starch branching enzyme!
It is important to remember that a gene does not directly
generate a protein. As shown previously in Figure 1.2, a
gene codes for an RNA, which may in turn code for a protein. Most genes code for
proteins, but some genes code for RNAs that do not give rise to proteins. These
RNAs may be structural components of the apparatus responsible for synthesizing
proteins or may have roles in regulating gene expression. The basic principle is
that the gene is a sequence of DNA that specifies the sequence of an independent
product. The process of gene expression may terminate in a product that is
either RNA or protein.
A mutation is a random event with regard to the structure of
the gene, so the greatest probability is that it will damage or even abolish
gene function. Most mutations that affect gene function are recessive: they
represent an absence of function, because the mutant gene has been prevented
from producing its usual protein.
Figure 1.26
illustrates the relationship between recessive and wild-type alleles. When a
heterozygote contains one wild-type allele and one mutant allele, the wild-type
allele is able to direct production of the enzyme. The wild-type allele is
therefore dominant. (This assumes that an adequate amount of protein is
made by the single wild-type allele. When this is not true, the smaller amount
made by one allele as compared to two alleles results in the intermediate
phenotype of a partially dominant allele in a heterozygote.)
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