dna & protein synthesis Flashcards
1
Q
what is DNA?
A
- dna is the molecule that carries genetic information for the development & functioning of an organism
-dna found in all living things and codes for the instructions that makes an organism
1
Q
what does DNA stand for?
A
- Deoxyribonucleic acid
2
Q
nucleotides are made up of?
A
- made up of 3 parts
- phosphate group + deoxyribose sugar + nitrogenous base
3
Q
nucleotides
A
- A= adenine, T= thymine, G= guanine, C= cytosine
- joined together by their sugar phosphate backbones
- hydrogen bonds (weak bonds) hold together the nitrogenous bases
4
Q
how genes make a protein
A
- enzyme: a protein that speeds up chemical reactions
- DNA polymerase: an enzyme that helps copy dna during cell division (mitosis) DNA -> DNA
- RNA polymerase: an enzyme that helps copy dna during protein synthesis. its converts DNA to RNA
5
Q
RNA
A
- rna uses ribose sugar instead of deoxyribose
- has 4 base pairs: instead of thymine it has uracil
- A pairs with U and G pairs with C
- single stranded and short
- RNA can leave the nucleus and travel into cytoplasm
- 3 types: mRNA, rRNA, tRNA
6
Q
two steps of protein synthesis
A
- transcription (DNA -> mRNA)
- translation (mRNA -> protein)
7
Q
what is mRNA
A
- stands for messanger RNA
- mRNA carries the instructions for one gene
- mRNA is synthesised in the the nucleus
8
Q
what is the function of mRNA
A
- its function is to make a copy of a gene and take it to a ribosome (found in cytoplasm), where amino acids are assembled to make a protein
9
Q
transcription- DNA to mRNA
A
- transcription is the first of gene expression/protein synthesis
- it is broken into three major steps
1. initiation
2. elongation
3. termination
10
Q
initiation
A
- initiation is the beginning of transcription. it occurs when the enzyme RNA polymerase binds to a region of a gene called the promoter
- this signals the DNA to unwind so the enzyme can ‘read’ the bases in one of the DNA stands (known as the template strand)
- the enzyme is now ready to make a strand of mRNA and complementry sequence of bases
11
Q
elongation
A
- elongation is when complementary nucleotides are added to synthesise an mRNA strand
- RNA polymerase reads the unwound DNA strand & builds the mRNA molecule, using complementary base pairs
- adenine pairs with uracil & cytosine pairs with guanine
12
Q
termination
A
- termination is the ending of transcription, and occurs when RNA polymerase crosses a termination sequence in the gene
- the mRNA strand is complete, and it detaches from RNA
13
Q
the three steps together
A
- the mRNA strand is now ready to leave the nucleus, travel into the cytoplasm, attach a ribosome and to be translated into a protein
14
Q
first three steps of translation- mRNA to protein
A
- the mRNA moves through the nuclear pore to the cytoplasm
- the mRNA attaches to the ribosome. the ribosome moves along the mRNA strand, reading 3 nucleotides (condon) at a time. translation begins at the START condon.
- transfer RNA (tRNA) molecules ferry the amino acids to the mRNA at the ribosome
15
Q
last three steps of translation- mRNA to protein
A
- tRNA links with the ribosome and matches its anticondon of mRNA
- a peptide bond forms between the adjoining amino acids, forming a polypeptide. The tRNA is removed to be used again
- the protein production stops when a STOP condon is reached. the mRNA breaks away from the ribosome. STOP condons are UAA, UGA, UAG. THey aer STOP condons because they don’t code for anything
16
Q
how does the coding work?
A
- each codon codes for an amino acid
- there are 20 amino acids, so some are coded for by multiple codons
17
Q
DNA mutations (causes & how common)
A
- mutations occur at a frequency of about 1 in every billion base pairs
- everybody has about 6 mutations in their body
- mutations aren’t always seen, the affected gene may still be able to function
- muations may be: harmful, beneficial
18
Q
how does mutations impact protein synthesis?
A
- DNA affect= substitution, insertion, deletion
- mRNA copied incorrectly
- codes for wrong amino acids
- formation of incorrect protein/part of polypeptide is missing/ not functioning protein
19
Q
what are mutations
A
- mutations are changes in genetic material; changes in DNA and gene/s
- in mutations, the DNA code can have 1 or more bases: added, deleted, or exchanged
20
Q
causes of mutations
A
- mutations may occur randomly & spontaneously due to errors in DNA replication
- they may be induced by mutagens. e.g. x-ray and uv lights
21
Q
names of genetic mutations
A
- Huntingtons disease (insertion DNA mutation)
- Sickle cell anaemia (substitution DNA mutation)
22
Q
what is huntingtons disease?
A
- a progressive brain disorder that affects the central area of the brain
- movement, mood and thinking skills are affected as a consequence
23
Q
changes in DNA segment for huntingtons disease
A
- mutation involves a DNA segment of cytosine, adenine, and guanine that appears multiple times in a row
- normally CAG segment is repeated 10 to 35 times within a gene
- in people with huntingtons the segment is repeated more than 120 times
24
what is sickle cell anaemia?
- only one amino acid changes in the haemoglobin
- the haemoglobin still functions but it folds differently, changing the shape of the red blood cell
- this affects the way the haemoglobin can carry oxygen
25
what are some possible genetic disorders?
- cystic fibrosis
- klinefelter (XXY)
- tourette syndrome
- turner syndrome
- down syndrome