Central Dogma, Transcription, Translation, and Mutations in Molecular Biology

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23 Terms

1
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What does the Central Dogma of Molecular Biology state?

Genes specify the sequences of mRNAs, which in turn specify the sequences of amino acids in proteins.

2
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What are the two processes involved in the Central Dogma?

Transcription and translation.

3
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What is the structure of DNA?

DNA is a double helix that stores genetic information in the form of nucleotides.

4
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What are the three stages of transcription?

Initiation, elongation, and termination.

5
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What occurs during the initiation stage of transcription?

The DNA double helix partially unwinds, and RNA polymerase binds at the promoter.

6
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What is a promoter in the context of transcription?

A short sequence of DNA nucleotides that bind to start the transcription process.

7
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What happens during the elongation stage of transcription?

RNA polymerase adds RNA nucleotides by base pairing with the DNA template.

8
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What is the DNA template used for during transcription?

Only one DNA strand is used during transcription.

9
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What signals the termination of transcription?

The polymerase is instructed to dissociate from the DNA template.

10
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What is the start codon in translation?

AUG is the start codon.

11
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What are the three compartments of the large ribosomal subunit during translation?

The A, P, and E sites.

12
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What is an anti-codon?

An anti-codon is a sequence on tRNA that matches with a codon on mRNA.

13
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What occurs during the termination stage of translation?

Translation is complete when a stop codon (UAA, UAG, or UGA) is encountered, releasing the polypeptide.

<p>Translation is complete when a stop codon (UAA, UAG, or UGA) is encountered, releasing the polypeptide.</p>
14
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What does the universal genetic code imply?

Virtually all species use the same genetic code for protein synthesis.

15
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What is a mutation?

A change in the DNA sequence of a gene.

16
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How can mutations affect proteins?

Mutations can change the sequence of amino acids in a protein, potentially modifying or destroying its function.

17
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What is the difference between genotype and phenotype?

Genotype is an organism's genetic makeup, while phenotype is the observable trait.

18
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What is a gene?

A specific region on DNA that codes for a polypeptide.

19
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What is a locus?

The physical location of a gene on a chromosome.

20
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What is an allele?

Alternative forms of the same gene.

21
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What distinguishes homozygous individuals from heterozygous individuals?

Homozygous individuals have two copies of the same allele, while heterozygous individuals have two different alleles.

22
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How can a mutation in DNA lead to a phenotypic change?

By altering the protein's function or structure, leading to a different trait.

23
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What specific mutation causes sickle cell disease?

A mutation that changes one amino acid (glutamic acid to valine) in the hemoglobin protein, causing it to clump together under low oxygen conditions.