Chapter 8 Protein Synthesis • MHR 253
genetic code codons are made up of nucleotide
triplets, is known as the triplet hypothesis.
Crick tested his hypothesis by inserting different
numbers of nucleotides into bacterial DNA and
then observing the effects on the resulting bacterial
colonies. If his triplet hypothesis was correct,
the insertion of a new nucleotide triplet would
produce only a minor disruption in the coding
sequence. In contrast, the insertion of a single
nucleotide or a pair of nucleotides would cause a
major change in the triplet sequence following the
insertion point, as shown in Figure 8.2. The results
of Crick’s experiments, which were reported in
1961, supported the triplet hypothesis.
Figure 8.2A schematic of Crick’s experiments to test the
triplet hypothesis
The Transfer of
Genetic Information
Before they discovered the structure of DNA,
Watson and Crick had started to devise a theory
that genetic information is somehow transmitted
from DNA to RNA and then to proteins. Part of the
supporting evidence for this sequence of events lay
in experiments that demonstrated that DNA never
leaves the nucleus of a eukaryotic cell. These
experiments also showed that most of the structures
and processes involved in protein synthesis are found
only in the cytoplasm of the cell. RNA, however, is
found in both the nucleus and the cytoplasm.
Not long after Watson and Crick had established
their model for the structure of DNA and its
process of replication, Francis Crick coined the
phrase “central dogma” to describe the two-step
process by which he believed genes were expressed
and proteins built. According to this dogma, a term
he used to suggest a powerful theory that had
little experimental support, a strand of DNA first
serves as the template for the construction of a
complementary strand of RNA. This strand of RNA
then moves from the nucleus to the cytoplasm.
Here, it guides the synthesis of a polypeptide
chain. Over the next few years, experimental data
confirmed that genetic information is indeed
passed from DNA to RNA to protein.
Figure 8.3 summarizes the two main steps
involved in the process of gene expression. The
synthesis of an RNA molecule from a strand of DNA
is called transcription. To transcribe means to make
a copy of or otherwise transfer information from
one medium to another in a way that preserves the
original language of the information. During genetic
transcription, the nucleotide sequence (the language)
of the DNA strand is copied into the nucleotide
sequence of the synthesized RNA molecule. In
contrast, during the second step, called translation,
the language preserved in the RNA must be
converted to the amino acid sequence of a
polypeptide in order for a protein to be synthesized.
You will learn more about each of these steps later
in this chapter.
Figure 8.3Crick’s “central dogma” proposes a two-step
process of gene expression. In this process, genetic
information is first transcribed from DNA to RNA, and
then translated from RNA to protein.
Why does DNA not code directly for a
polypeptide product? At first glance, the two-step
process seems like an unnecessary waste of cellular
energy. However, the additional energy involved in
producing an RNA copy of the DNA information is
DNA
protein
RNA
transcription translation
TAG TAG TAG TAG TAG TAG
CTA GTA GTA GTA GTA GTA
CCT
or
AGT AGT AGT AGT AGT
TAG CCC TAG TAG TAG TAG
TAG
or
normal
bacterial
colonies
no
colonies
mutant
TCC CAG TAG TAG TAG colonies
This is a normal bacterial coding sequence for a
hypothetical polypeptide product. Normal bacteria
reproduce in viable colonies.
A
The insertion of a single nucleotide or a pair of
nucleotides alters all subsequent nucleotide triplets. No
viable colony is produced, indicating that the insertion
has caused a mutation so severe that the bacteria are
unable to manufacture a functioning polypeptide.
B
The insertion of a nucleotide triplet alters at most two
“words” of the code, after which the normal coding
sequence resumes. The result is viable but mutant
colonies that manufacture a modified version of the
polypeptide.