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Key Concepts
17.1 Genes specify proteins via transcription and translation
17.2 Transcription is the DNA-directed synthesis of RNA: a closer look
17.3 Eukaryotic cells modify RNA after transcription
17.4 Translation is the RNA-directed synthesis of a polypeptide: a closer look
17.5 RNA plays multiple roles in the cell: a closer look
17.6 Comparing gene expression in prokaryotes and eukaryotes reveals key differences
17.7 Point mutations can affect protein structure and function
Interactive Questions
Met-Pru-Asp-Phe-Lys-STOP
Using some of the codons and the amino acids you identified in Interactive Question
17.2, fill in the following table.
1. Codon Recognition
2. Peptide Bond Formation
3. Translation
4. Termination
a. mRNA Carries the code from DNA that specifies the amino acid
b. tRNA Carries a specific amino acid to its position in a polypeptide
c. rRNA Plays catalytic (ribozyme) roles and structural roles in ribosomes
d. snRNA Small nuclear RNA, part of the spliceosomes, splices mRNA
e. SRP RNA Signal recognition particle that binds to signal peptides bound to
endoplasmic reticulum
f. snoRNA (small nucleolar RNA) Aids in processing pre-RNA transcript in
nucleolus
g. siRNA (small interfering RNA) and miRNA (microRNA) small interfering
RNA
Define the following, and explain what type of point mutation could cause each of these
mutations.
a. silent mutation A base pair substitution that produces a codon that still codes for
the same amino acid
b. missense mutation Base pair substitution or frameshift mutation that results in a
codon for a different amino acid
c. nonsense mutation Base pair substitutions or frameshift mutation that creates a
stop codon and prematurely terminates translation
d. frameshift mutation An insertion or deletion of one, two, or more, than three
mucleotides that disrupts the reading frame and creates extensive missense or
nonsense mutations
Structure Yo Knowledge
1.
Transcription Translation
Template DNA RNA
Location Nucleus (eukaryotes) Cytoplasm
Molecules involved RNA nucleotides, DNA Amino acids, tRNA,
template strands, RNA mRNA, ribosomes, ATP,
polymerase, transcription GTP, enzymes, initiation
factors elongation
Enzymes involved RNA polymerase, Aminoacyl-tRNA
ribozymes synthetase
Control start and stop Transcription factors, TATA Initiation factors, AUG, stop
box, poly A codons, release factors
Product Primary transcript (pre- Protein (polypeptide)
mRNA)
Product processing RNA processing: 5 cap, Spontaneous folding,
poly A tail, splicing disulfide bridges, cleaving,
structure
Energy source RIbonucleoside, ATP, GTP
triphosphate
2. The genetic code is the RNA triplets that code for amino acids. The order of these
codons is specified by the sequence of nucleotides on DNA, which is transcribed into the
codons found on mRNA and translated into their corresponding amino acids. There are
64 possible mRNA codons created from the our nucleotides used in the triplet code (43)
Redundancy of the code refers to the fact that several triplets may code for the same
amino acid. Often these triplets differ only in the third nucleotide. The wobble
phenomenon explains the fact that there are only about 45 different tRNA molecules that
pair with the 61 possible codons (three codons are always stop codons). The third
nucleotide of many tRNAs can pair with more than one base. Because of the redundancy
of the genetic code, these wobble tRNAs still place the correct amino acid in position.
3.
POINT MUTATIONS
base-pair may be
substitutions may be
due to
insertions spontaneous mutagens
may have or deletions
small effect
on protein usually have during may be