← Genetics Lecture 1 Test
5 Written Questions
5 Matching Questions
- where does transcription occur
- components of a typical gene
- how many pairs of autosomal and sex-determining chromosomes do humans normally have?
- name the two pyrimidines in DNA
- what are the steps in transcription
- a 22 autosomal, 1 sex-determining
- b T,C
- c 5' end, promoter region, alternating exon and intron regions, 3' end
- d 1. initiation - the catalyst RNA polymerase binds to promoter sequence and 'opens' the DNA
2. elongation - RNA polymerase advances 3' to 5' creating a complementary strand of RNA
3. termination - RNA polymerase reaches a stop codon and release completed RNA. Dissociates from DNA - e in the nucleus
5 Multiple Choice Questions
- cellular machinery makes a copy of the DNA called mRNA, the mRNA is then used as a template for making a protein
- in the nucleus
- adenine, thymine, guanine, cytosine
- reading of mRNA; the translating of the mRNA into a string of amino acids to make a protein
- in the nucleus
5 True/False Questions
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implication of the central dogma for understanding genetic diseases → information flow goes in one direction only: DNA --> mRNA --> protein
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what does 1 gene code for? → 1 protein
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definition of the human genome → 5' end, promoter region, alternating exon and intron regions, 3' end
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what are the two types of chromosomes humans have? → 1. ribosome traverses mRNA
2. tRNAs are added that code for specific amino acids
3. protein is assembled by adding peptide bonds to the growing amino acid chain -
how does the 3rd position wobble arise? → arises from the redundancy in the genetic code, whereby multiple 3-letter combinations code for the same amino acid, therefore in some cases a mutation in the 3rd position won't affect the coding
Regenerate Test