GENETIC INFORMATION, VARIATION & RELATIONSHIPS BETWEEN ORGANISMS Flashcards
What are the differences between DNA in eukaryotes and prokaryotes?
Eukaryotic DNA:
- long & linear, wound up
- wound around proteins called histones (help support DNA)
- held in nucleus
- mitochondria & chloroplasts have their own DNA, circular & short, not associated with histones (similar to prokaryotic DNA)
Prokaryotic DNA:
- short & circular
- isn’t wound around histones, condenses to fit by supercoiling
- held in cytoplasm
What is a gene?
Base sequence of DNA that codes for polypeptide or functional RNA.
- Order of bases in a gene determine order of amino acids in polypeptide
- Each amino acid coded by sequence of three bases in a gene = triplet
What is a genome?
Complete set of genes in the cell
What is a proteome?
Full range of proteins that the cell is able to produce
What is the genetic code?
Sequence of bases in length of DNA code for sequence of amino acids in polypeptide or functional RNA
What are characteristics of the genetic code?
Degenerate- more than one codon can code for the same amino acid
Universal- same specific base triplets code for the same amino acids in all living things
What are exons?
Areas that code for amino acids within the genes
What are introns?
Areas that are non-coding, do not code for a polypeptide
What is a mutation?
- Any change to the quantity or base sequence of the DNA of an organism
- If mutation occurs during formation of gametes, it may be inherited and cause a dramatic change to a species
What is a gene mutation?
Any change to 1 or more nucleotide bases or a change in the sequence of bases of the DNA
What is a base substitution and what is its effect?
- If a base is replaced with another nucleotide that has a different base
- Effect depends on base that’s changed. If it changed the amino acid, the polypeptide will be a different shape so no longer have its function.
- Sometimes there’s no change in amino acid due to degenerate nature of genetic code
What is a base deletion / addition and what is its effect?
- A gene mutation caused when a nucleotide is lost from or added to the normal DNA sequence
- Causes a frame shift, all the triplets from that point on will be affected
What is a chromosome mutation and what are the 2 types?
Changes in the structure or number of whole chromosomes
- Changes in whole sets of chromosomes
- condition called polyploidy, organism has 3 or more sets of chromosomes rather than the normal 2 - Changes in number of individual chromosomes
- where homologous pairs of chromosomes do not separate during meiosis (non-disjunction), so one gamete gets 1 extra chromosome and one gets 1 less
What is variation?
- Means ‘differences’ between individuals in a species
- Helps a species adapt to a changing environment for survival
How do you get variation?
- Sexual reproduction
- Mutations
What is meiosis and what does it produce?
Cell division to form a gamete (sex cell)
- forms 4 daughter cells that are haploid (half the number of chromosomes of the parent cell), only containing 1 set of chromosomes so when fertilisation occurs the normal amount of chromosomes is restored
What is the process of meiosis?
FIRST DIVISION
Interphase:
- Chromosomes are not visible
- Chromosomes start to replicate & become visible
Prophase 1:
- Chromosomes condense
- Nuclear envelope breaks down
- Crossing over occurs between homologous chromosomes
Metaphase 1:
- Pairs of homologous chromosomes move to equator of cell, attached via centromeres on spindle fibres
- Arrange themselves randomly (independent assortment)
Anaphase 1:
- Homologous chromosomes move to opposite poles of cell as spindle fibres contract
Telophase 1:
- Nuclear membrane starts to reform
- Chromosomes gather at poles of cells
Cytokinesis 1:
- Cytoplasm divides, 2 daughter cells are formed
SECOND DIVISION
Prophase 2:
- Nuclear membrane disappears
- Centreioles produce new spindle fibres which form around chromosomes and attach to centromeres
Metaphase 2:
- Chromosomes randomly line up at equator
Anaphase 2:
- Centromeres divide
- Spindle fibres contract, pulling sister chromatids to opposite poles of cell
Telophase 2:
- Nuclear envelop reforms around chromatids
- Cytoplasm begins to divide
Cytokinesis 2:
- Cytoplasm divides
- 4 genetically different haploid daughter cells are produced
What is non-disjunction and what are its effects?
‘Failure to separate’
- Where homologous chromosomes or sister chromatids don’t separate properly during meiosis
- The effects vary depending on chromosomes affected, but often very serious
How does non-disjunction lead to downs syndrome?
- Non-disjunction of chromosome 21 (2 copies of chromosome 21)
- During fertilisation, if 1 gamete within 2 copies of chromosome 21 fuses with a gamete with a normal number of chromosomes, the result is a cell with 3 copies of chromosome 21, resulting in downs syndrome