10.9 the beginning of a gene and five different mutations of this the base-pairing rules to complete the second column. For each mutation, write in any mRNA codons that will be changed as a result of the mutation and use "X" marka to Indicate codons that will not be changed. Use the codon wheel on page 10.11 to identify any stop codons in the MRNA molecules. Circle the stop codons. Use the codon wheel to complete the last column. For each mutation, write in any amino acids that will be changed and use "X" marks to indicate any amino acids that will not be changed. Use dashes to indicate any amino acids that will be missing as a result of a stop codon. Beginning of gene in DNA First five mRNA codons Beginning of Protein Original DNA = TACGCAAGTACCTGA... AUG CGU UCA Met – Arg- Ser - Trp-Thr UGG ACU Mutation 1 = TACGCCAGTACCTGA... (nucleotide change underlined) Mutation 2 = TACGCACGTACCTGA... (nucleotide change underlined) Mutation 3 = TACGCAAGTACITGA... (nucleotide change underlined) Mutation 4 = TACGAAGTACCTGA... (second C deleted) TACGCAAGTACTGA... (third C deleted) Mutation 5 =
10.9 the beginning of a gene and five different mutations of this the base-pairing rules to complete the second column. For each mutation, write in any mRNA codons that will be changed as a result of the mutation and use "X" marka to Indicate codons that will not be changed. Use the codon wheel on page 10.11 to identify any stop codons in the MRNA molecules. Circle the stop codons. Use the codon wheel to complete the last column. For each mutation, write in any amino acids that will be changed and use "X" marks to indicate any amino acids that will not be changed. Use dashes to indicate any amino acids that will be missing as a result of a stop codon. Beginning of gene in DNA First five mRNA codons Beginning of Protein Original DNA = TACGCAAGTACCTGA... AUG CGU UCA Met – Arg- Ser - Trp-Thr UGG ACU Mutation 1 = TACGCCAGTACCTGA... (nucleotide change underlined) Mutation 2 = TACGCACGTACCTGA... (nucleotide change underlined) Mutation 3 = TACGCAAGTACITGA... (nucleotide change underlined) Mutation 4 = TACGAAGTACCTGA... (second C deleted) TACGCAAGTACTGA... (third C deleted) Mutation 5 =
Biology 2e
2nd Edition
ISBN:9781947172517
Author:Matthew Douglas, Jung Choi, Mary Ann Clark
Publisher:Matthew Douglas, Jung Choi, Mary Ann Clark
Chapter15: Genes And Proteins
Section: Chapter Questions
Problem 18RQ: A scientist introduces a mutation that makes the 60S ribosomal subunit nonfunctional in a human cell...
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Question
PLEASE FL OUT TABLE USING INSTRXUTIONS
-USE BASE PAIRING RULES TO COMPLETE SECOND COLUMN FOR EACH MUTATION WRIYE IN ANY MRNA DOEONS RHAT WILL BE FHANGED AS THE REEULR OF RHE MURATION AND USE X MARKS RO INDÍCATE DOONS THAT WONT BE FHANGES
CIRCLE STOP CODONS
Transcribed Image Text:10.9
the table belaw shows the beginning of a gene and five different mutations of this
part of the gene. Use the base-pairing rules to complete the second column, For each mutation,
write in any mRNA codons that wiIl be changed as a result of the mutation and use "X" maka to
Indicate codons that will not be changed.
Ose the codon wheel on page 10.11 to identify any stop codons in the MRNA molecules. Circle the
stop codons.
Use the codon wheel to complete the last column. For each mutation, write In any amino acids that
will be changed and use "X" marks to indicate any amino acids that will not be changed. Use
dashes to indicate any amino acids that will be missing as a result of a stop codon.
Beginning of gene in DNA
First five mRNA codons
Beginning of Protein
Original DNA =
TACGCAAGTACCTGA... AUG CGU UCA
Met - Arg- Ser -
Trp- Thr
UGG ACU
Mutation 1 =
TACGCCAGTACCTGA...
(nucleotide change underlined)
Mutation 2 =
TACGCACGTACCTGA...
(nucleotide change underlined)
Mutation 3 =
TACGCAAGTACITGA...
(nucleotide change underlined)
Mutation 4 =
TACGAAGTACCTGA...
(second C deleted)
Mutation 5 =
TACGCAAGTACTGA...
(third C deleted)
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