Unit 4 Flashcards
Describe the role of DNA.
Carries genetic information, determines
our inherited characteristics.
Describe the structure of RNA.
func=Transfers genetic information from DNA to ribosomes for protein synthesis.
Made up of a ribose sugar, a phosphate
group, and one of four organic bases (A,C,G,U).
It is single stranded.
How is DNA in eukaryotic cells different from in prokaryotic cells?
● Eukaryotic cells=
-found in nucleus
-long and linear
-Associated with histone proteins to form chromosomes.
Mitochondria and chloroplasts
contain prokaryotic-like DNA.
● Prokaryotic cells= short and circular.
Not associated with proteins.
What is the genetic code?
Order of bases on DNA
Consists of codons (triplets of bases that code for a particular amino acid
Identify features of the genetic code 3
● Non-overlapping= each triplet is only read once.
● Degenerate= more than one triplet (codon) codes for the
same amino acid
● Universal= same bases and sequences used by all species
What is a gene? 3
A sequence of bases on a DNA molecule
- that codes for a specific sequence of amino acids to make a polypeptide.
Can also code for functional RNA.
What is a locus?
The fixed position on a DNA molecule occupied by a gene
What is an allele?
Different versions of the same gene, found at the same locus on a
chromosome
What are exons and introns?
(introns, between exons within genes)
Exons= regions of DNA that code for amino acid sequences. Separated by
one or more introns.
Introns= regions of DNA that do not code for anything.
What is the genome?
The complete set of genetic information contained in the cells of an organism
What is the proteome?
The complete set of proteins that can be produced by a cell.
Describe the structure of messenger RNA (mRNA) 4
-long
-uracil instead of thymine
-single strand
-Its base sequence is complementary to the DNA it was
transcribed from
Suggest advantages of using mRNA rather than DNA for translation. 3
● shorter & contains uracil = breaks down quickly so no excess polypeptide forms
● single-stranded & linear = ribosome moves along strand & tRNA binds to exposed bases
● contains no introns
Describe the structure of transfer RNA
(tRNA).
-A single strand of around 80 nucleotides
- folded over into a clover leaf shape
-one end is an anti-codon
-on the opposite end is an amino acid binding site
Outline the process of transcription happens in the nucleus 6
the production of mRNA from DNA
RNA polymerase in joining mRNA nucleotides.
-Hydrogen bonds between DNA bases break
-Only one DNA strand act as a template
-Free adjacent RNA nucleotides align by complementary base pairing
-In RNA, Uracil is used instead of thymine
-RNA polymerase joins RNA nucleotides together by phosphodiester bonds from pre-mRNA
-pre-mRNA is spliced to remove introns, forming mRNA
What happens to mRNA after transcription (copy)?2
-In eukaryotic cells, pre-mRNA must be spliced to remove introns, leaving only the coding regions.
-Then it moves out of the nucleus and attaches to a ribosome
Outline the process of translation. 7
-happens in the cytoplasm on ribosomes
-proteins produced
-mRNA attaches to ribosomes
-tRNA anticodons bind to complementary mRNA codons
-tRNA brings a specific amino acid.
-Amino acids join by peptide bonds.
-Amino acids join together with the use of ATP
-tRNA released after amino acid joined to the polypeptide
-The ribosome moves along the mRNA to form the polypeptide;
What is a mutation
An alteration to the DNA base sequence.
Often arise spontaneously during DNA
replication.
Why might a mutation not lead to change in the amino acid sequence?
● Genetic code is degenerate so
mutation may end up coding for same
amino acid as the original triplet.
● Mutation may occur in intron.
What is a substitution mutation?
-genetic code degenerate so not all substitions result in a change in the primary structure of a polypeptide chain
When a nucleotide in the DNA sequence is replaced by another. This is more likely to be a quiet mutation, meaning no change occurs in the amino acid sequence
What is a deletion mutation
- nucleotide in the DNA sequence
is lost.
-leads to a frame shift
-entire amino acid sequence will be different.
What is a mutagenic agent? Give
examples of this 2
-Factors that increase the rate of gene
mutation.
-X-rays, UV light, gamma rays,
certain chemicals e.g. in alcohol and
tobacco.
What is chromosome non-disjunction?
chromosomes/ chromatids fail to separate correctly in meiosis resulting in gametes with one more or less chromosome than normal
-in anaphase 1 /meiosis homologous pairs fail to separate and are not pulled to opposite poles
-in anaphase 2 sister chromatids fail to separate and are not pulled to opposite poles
What is meiosis?2
-A form of cell division
-produces four
genetically different haploid cells (cells with half the number of chromosomes found in the parent cell) known as gametes.
How does meiosis differ from mitosis?2
● Meiosis produces four genetically different cells with half the number of chromosomes as the parent cells.
● Mitosis produces two genetically identical cells with the same number of chromosomes as the parent cells
What happens during meiosis Ⅰ?3
- Homologous chromosomes pair to form bivalents.
- Crossing over (exchange of sections of genetic material) occurs at chiasmata.
- Cell divides into two. Homologous chromosomes separate randomly. Each cell contains either
maternal or paternal copy.