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From DNA to Proteins
Beyond
Byssus
A. Byssus, a fantastic underwater adhesive,
is a protein, synthesized in accordance with the message encoded in
the base sequences of DNA.
B. DNA is like a book of instructions
written in the alphabet of A, T, G, and C, but merely knowing the letters
does not tell us how the genes work.
C. It takes two processes–transcription
and translation–plus a critical role played by RNA to synthesize
proteins.
1. In transcription, molecules of RNA are produced on the DNA templates
in the nucleus.
2. In translation, RNA are molecules shipped from the nucleus to the
cytoplasm to be used in polypeptide assembly.
I.
How Is DNA Transcribed Into RNA?
A. The Three Classes of RNA
1. Messenger
RNA (mRNA) carries the
"blueprint" to the ribosome.
2. Ribosomal
RNA (rRNA) combines with
proteins to form ribosomes upon which polypeptides are assembled.
3. Transfer
RNA (tRNA) brings the correct
amino acid to the ribosome and pairs up with an mRNA code for that amino
acid.
B. The Nature of Transcription
1. RNA differs from DNA in
some ways:
a. RNA uses ribose
sugar, not deoxyribose.
b. RNA bases are
A, G, C, and uracil (U).
2. Transcription differs from
DNA replication in three ways:
a. Only one region of one DNA strand is used as a template.
b. RNA polymerase
is used instead of DNA polymerase.
c. The result
of transcription is a single-stranded RNA.
3. Transcription begins when
RNA polymerase binds to a promoter region (a base sequence at the start
of a gene) and then moves along to the end of a gene; an RNA transcript
is the result.
C. Finishing Touches on mRNA Transcripts
1. Newly formed mRNA is modified
by the addition of a cap to the 5Õ end (a "start" signal for
protein synthesis) and a poly-A tail to the 3Õ end.
2. Additionally, the mRNA
transcript must be edited.
a. The introns (noncoding portions) are removed before the transcript leaves the nucleus.
b. Only the exons (portions that will eventually be translated) remain in the finished
transcript that leaves the nucleus.
II.
Deciphering the mRNA Transcripts
A. What Is the Genetic Code?
1. Both DNA and its mRNA transcript
are linear sequences of nucleotides carrying the hereditary code.
2. Every three bases (a triplet)
specifies an amino acid to be included into a growing polypeptide chain;
this is called the genetic
code.
a. The genetic
code consists of sixty-one triplets that specify amino acids and three
that serve to stop protein synthesis.
b. Each base triplet
in RNA is called a codon.
c. With few exceptions,
the genetic code is universal for all forms of life.
B. Structure and Function of tRNA and
rRNA
1. Translation occurs on the
surface of ribosomes (rRNA + proteins) composed of two subunits that
unite during translation.
2. Each kind of tRNA has an
anticodon that is complementary to an mRNA codon and also carries one
specific amino acid.
3. After the mRNA arrives
in the cytoplasm, an anticodon on a tRNA bonds to the codon on the mRNA,
and thus a correct amino acid is brought into place.
III.
How Is mRNA Translated?
A. Stages of Translation
1. In initiation, a complex forms in this sequence: initiator tRNA
+ small ribosomal subunit + mRNA + large ribosomal subunit.
2. In elongation, a start codon on mRNA defines the reading frame;
a series of tRNAs deliver amino acids in sequence by codon-anticodon
matching; a peptide bond joins each amino acid to the next in sequence.
3. With termination, a stop codon is reached and the polypeptide chain
is released into the cytoplasm or enters the cytomembrane system for
further processing.
B. What Happens to the New Polypeptides?
1. In cells that are rapidly
making proteins, polysomes consisting of many ribosomes are translating
the same mRNA transcript to make polypeptides in a hurry.
2. Newly synthesized polypeptides
either join the cytoplasmÕs pool of proteins or enter the cytomembrane
system in preparation for export.
IV.
Do Mutations Affect Protein Synthesis?
A. A gene mutation is a change in
one to several bases that may be added, deleted, or replaced in the
nucleotide sequence of DNA.
B. Common Gene Mutations and Their
Sources
1. An example of a spontaneous
mutation is sickle-cell anemia, which is the result of a single "base
pair substitution" which places valine as the sixth amino acid
in the hemoglobin chain instead of glutamate.
2. In a "frameshift mutation,"
there may be an insertion or deletion of several base pairs causing
a misreading of the mRNA during translation.
3. A rather dramatic mutation
is that of transposable elements, which are regions of DNA that "jump"
to new locations in DNA.
C. Causes of Gene Mutations
1. Many gene mutations are
spontaneous.
2. Others are caused
by mutagens such as UV light, ionizing radiation, and alkylating agents.
D. The Proof Is in the Protein
1. Spontaneous mutations are
rare and will not endure unless they occur in gametes.
2. A protein that is specified by a heritable mutation may have h |
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Created by
Aaron Neal |
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