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test 3 term 2
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DNA
Deoxyribonucleic acid - the chemical compound that carries the inherited information in the cell, codes for protein production
Nucleotide
The basic structural unit of DNA, consisting of a deoxyribose sugar, a phosphate and a nitrogen base.
Gene
A section of DNA, that codes for a particular trait
Chromatin
Highly coiled DNA molecule
Chromosome
Super coiled chromatin (DNA) to form a rod-like structure that contains the genes of an individual
DNA Replication
to carry the genetic code accurately and be able to pass it onto future generations, every cell must have identical DNA to the original body cell.
1.A representative portion of DNA, which is about to undergo replication
2.the two strands of the DNA separate. The hydrogen bonds between the bases break
3.Free nucleotides are attracted to their complementary bases
4.Once the new nucleotides have lined up, they are joined together by the enzyme DNA polymerase
5.finally, all the nucleotides are joined to form a complete polynucleotide chain using DNA polymerase. In this way, two identical strands of DNA are formed. As each strand retains half of the original DNA material, this method of replication is called the semi-conservative method
Protein
An organic compound made of amino acids that controls chemical reactions in the body.
Helicase
Enzyme responsible for separating the two sides of the
DNA molecule
DNA Polymerase
Enzyme involved in attaching loose nucleotides
to the exposed DNA strand
DNA Ligase
Enzyme involved in repairing the bonds that hold the backbone of the nucleotides together to form DNA
Allele
An alternative form of a gene that occurs at a given point in a chromosome
Dominant
Where one allele masks the effect of the alternative allele
Recessive
The allele which is only shown if it is not masked by the effects of a dominant allele
Genotype
The genes present in an individual, usually represented by letters eg. RR, Rr, rr
Phenotype
The physical appearance of an individual as determined by its genotype. eg. Tongue rolling and non tongue rolling
Homozygous
Where an individual has two identical alleles for a given gene
Heterozygous
Where an individual has two different alleles for a given gene
Punnett square
A table used to solve genetic problems
Sex-linked trait
A trait controlled by a gene found on a sex chromosome (usually the X chromosome).
X chromosome
One of the sex chromosomes; carries many genes.
Y chromosome
The smaller sex chromosome; carries fewer genes.
X-linked inheritance
When a gene is located on the X chromosome.
Carrier
A person who has one copy of a faulty gene but does not show symptoms.
Affected
A person who shows the trait or disease.
Dominant
A gene that only needs one copy to be expressed.
Recessive
A gene that needs two copies to be expressed (in females).
Pedigree
A diagram that shows how a trait is passed through a family.
Generation
A level in a pedigree (e.g. grandparents, parents, children).
Individual
One person in the pedigree.
Trait
A characteristic that can be inherited.
Inheritance pattern
The way a trait is passed from parents to offspring.
Cell cycle
The series of stages a cell goes through as it grows and divides.
Mitosis
The process where one cell divides to make two identical cells.
Interphase
The stage before mitosis where the cell grows and copies its DNA.
Chromosome
A structure made of DNA that carries genetic information.
Chromatid
One half of a duplicated chromosome (two identical halves joined together).
Sister chromatids
The two identical copies of a chromosome joined in the middle.
Centromere
The point where sister chromatids are attached.
Cytokinesis
The cell splits into two identical daughter cells.
Daughter cells
The two new cells formed after mitosis (genetically identical).
Nucleus
The part of the cell that contains DNA.
Spindle fibres
Thin structures that pull chromatids apart during mitosis.
Prophase
Chromosomes become visible and the nucleus starts to break down.
Metaphase
Chromosomes line up in the middle of the cell.