š DNA nucleotides A T C G genetic code (7 MCQs)
š From Campbell Biology ⢠1. Evolution and the theme of Biology and Scientific Inquiry ⢠7 questions available
What is DNA nucleotides A T C G genetic code?
Definition:
DNA nucleotides are the basic building blocks of DNA and contain a sugar, phosphate group, and nitrogenous base. The four DNA bases are adenine , thymine , cytosine , and guanine . Their sequence stores biological information.
Working:
DNA bases pair specifically, with pairing with , and pairing with . During gene expression, nucleotide sequences provide information used to determine protein sequences.
Example:
For a DNA sequence , the complementary sequence is . The pairing follows and rules.
Reason:
The order of nucleotides acts like biological information because different sequences can encode different instructions for producing functional molecules.
š All DNA nucleotides A T C G genetic code MCQs
Q1. A researcher identifies a DNA segment containing adenine, thymine, cytosine, and guanine. Which conclusion best explains why changing one nucleotide can sometimes alter a protein while another nucleotide change has little or no effect?
š Explanation: DNA nucleotides are read in groups of three during translation, producing codons that specify amino acids. Because multiple codons can encode the same amino acid, some substitutions are synonymous and produce no protein sequence change.
Q2. A DNA template contains the sequence 3'-TAC-GGA-CTT-5'. A student claims that the corresponding coding strand must read 3'-ATG-CCT-GAA-5'. What is the most accurate evaluation of the student's reasoning?
š Explanation: The coding strand is complementary to the template strand but runs antiparallel. Therefore, a template written 3' to 5' corresponds to a coding strand written 5' to 3' as 5'-ATG-CCT-GAA-3'.
Q3. A mutation changes an mRNA codon from 5'-GAA-3' to 5'-GAG-3'. Both codons specify glutamic acid. Which prediction is most reasonable if this is the only mutation?
š Explanation: The two codons differ at their third nucleotide but both encode glutamic acid. This illustrates redundancy in the genetic code, meaning a nucleotide substitution does not necessarily alter the amino acid sequence or protein structure.
Q4. A laboratory compares two DNA variants from the same gene. Variant X differs from the original at one nucleotide, while Variant Y differs at three nucleotides. Surprisingly, Variant X produces a different amino acid but Variant Y produces the same protein sequence. Which explanation best accounts for these results?
š Explanation: Protein consequences depend on where nucleotide changes occur and how they alter codons, not simply on mutation count. One substitution can change an amino acid, while several substitutions may be synonymous and leave the protein sequence unchanged.
Q5. A scientist records the percentage of mutations that change an amino acid in four regions of a gene: Region A = 72%, Region B = 48%, Region C = 21%, and Region D = 19%. Which interpretation is most defensible from these data?
š Explanation: A higher fraction of amino-acid-changing mutations can reflect differences in codon composition and substitution positions. However, the data alone cannot establish that a region is nonfunctional or mutation-free.
Q6. A mutation inserts one nucleotide near the beginning of a coding sequence. Several downstream codons are then interpreted differently from the original sequence. Why can the effect be much greater than that of a single nucleotide substitution?
š Explanation: Codons are interpreted as consecutive groups of three nucleotides. Adding one nucleotide changes the grouping of nearly all downstream bases, potentially altering many amino acids and creating a premature stop signal.
Q7. Two researchers propose models for predicting the effect of a single-base substitution. Model 1 considers only which nucleotide was changed. Model 2 considers the original codon, the new codon, and the reading frame. Which model should generally provide more reliable predictions, and why?
š Explanation: A nucleotide has no fixed amino-acid meaning by itself. Its effect depends on its position within a codon and the resulting codon sequence. Considering codon context therefore provides a biologically stronger prediction.