The bases always join onto the sugar in the nucleotide, never the phosphate
Hydrogen bonds
Weak bonds that connect the bases to each other
Chromosomes inherited from parents
2 sex chromosomes
44 autosomes
Some traits don't have a phenotype such as colour blindness because you can't see it on a person like you can with eye colour
More common for males to have sex linked diseases because the y chromosome doesn't possess any matching alleles
Y chromosome
Only contains information relevant to male features eg. Body hair and are smaller than other chromosomes
Gametes join together in fertilisation to create a zygote
Hydrogen bonds join the bases to each other
Mitosis
1. Interphase
2. Prophase
3. Metaphase
4. Anaphase
5. Telophase
6. Daughter cells
Meiosis
1. DNA replicates
2. Cell divides into 2 daughter cells
3. Two daughter cells divide creating 4 daughter cells each with half the required chromosomes needed in a diploid cell
DNA
Deoxyribonucleic acid
Nucleotide
Made up of sugar, phosphate, and base
Complementary base pairing
Adenine and Thymine always pair, Cytosine and Guanine always pair
Sex linked inheritance
Where the y chromosome doesn't carry a gene to express, several sex-linked diseases are caused by recessive genes on the x chromosome, which makes them more common in males than females
Simple Human Inheritance
Where characteristics are under the control of a single gene
Homologous pair
Same type of chromosome (corresponding chromosome one from the father, one from the mother)
Diploid number
The number of chromosomes in normal cells (46 in humans)
Haploid number
The number of chromosomes that gametes have which is half of what is needed to create a human. In humans the haploid number is 23
Bases
Adenine, thymine, cytosine and guanine. They each have a pair that they always match with, eg: g and c, T and a
Hydrogen bond
Weak chemical bonds that connect the bases to each other
Covalent bond
Stronger than hydrogen bonds and connects the nucleotides to each other and are formed by sharing electrons
Chromosome
Made of DNA and protein, are long threadlike structures found in the nucleus of most cells
Chromatid
One of two sides of the chromosome pair, joined at the centromere
Centromere
The place where two sister chromosomes are joined
Replication
The process of copying DNA. Where a cell makes a new copy of each chromosome, now that it has twice as many chromosomes as it should have, its ready to divide
Division
The process of cells dividing and creating new cells to make up an organism
Gamete
The sex cells (sperm and eggs), undergo meiosis, are known as haploid cells, have half the number of chromosomes as regular cells
Autosomes
44 of the 46 chromosomes in human cells, they determine characteristics
Sex cells
2 of the 46 cells in humans, they determine the sex of the person
Mitosis
The process of cells dividing to create two daughter cells, the chromosomes in the cell replicate themselves and then divide to create two new cells with the same amount of chromosomes as the parent cell
Meiosis
Occurs in haploid cells (gametes), produces cells that half the number of chromosomes than regular cells
Karyotypes
A chart of all the chromosomes in a diploid cell ( not sperm or egg), arranged in homologous pairs in order of size, centromere position and banding pattern, sex chromosomes are at the end
Allele
An alternate form of a gene
Recessive gene
An allele which can be masked by another allele, can only be expressed when two copies are present, is always written with the lower case
Dominant gene
The dominant allele is always written with an upper case, will always be expressed because it can't be masked by another allele
Homozygous
If an individual has two copies of the same alleles, prefix "homo' means 'same'
Heterozygous
An individual has two different alleles of a gene, prefix 'hetero' means 'other'
Incomplete dominance
When both alleles aren't dominant, eg. Red and white flower making a pink flower