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Flashcards for Year 10 Biology DNA lecture notes.
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Deoxyribonucleic acid (DNA)
A molecule that determines the genetic characteristics of most living things; it makes you who you are. Contains coded instructions that tell cells how to make proteins.
Nucleotides
Smaller molecules that make up DNA. They have three parts: a phosphate group, a deoxyribose sugar, and one of four nitrogen-rich bases.
Sugar-phosphate backbone
The backbone of a DNA strand, formed by nucleotides bonded together via the sugar and the phosphate group.
Nitrogenous bases
The bases that point inwards in DNA, forming a 'ladder' structure. There are 4 different nitrogenous bases: Adenine, Thymine, Cytosine, and Guanine.
Complementary binding
The way nitrogen bases bind together: Adenine only binds with thymine, and cytosine only binds with guanine.
DNA double helix
The twisted structure of DNA, like a twisted rope ladder, with sugar and phosphate molecules as the backbones and bases forming the rungs.
Gene
A section of DNA that contains the instructions for a specific protein.
Genetic code
The order of the nucleotide bases along the DNA strand, which codes for a specific protein.
Alleles
Different versions of genes; variations of genes that code for the same characteristic but have small changes in the way they are expressed.
Chromosomes
Long, thin, thread-like structures found in the nucleus of all cells, consisting of DNA wrapped around proteins. They are made of chromatin, which is DNA coiled tightly around proteins.
Somatic cells
Body cells that contain 46 chromosomes in humans.
Gametes
Eggs and sperm, which have only half as many chromosomes as body cells (23 chromosomes in humans).
Haploid nucleus
Nucleus has one chromosome of each type i.e. no homologous pairs. The cell contains 1 copy of every chromosome found in that species. A human haploid cell contains 23 chromosomes.
Diploid nuclei
Nuclei have 2 chromosomes of each type . The cell contains 2 copies of every chromosome found in that species. A human diploid cell contains 46 chromosomes.
Homologous chromosomes
Pairs of chromosomes that are similar in length, centromere position, shape, and contain the same genes (but may have different alleles). One is maternal, and one is paternal.
Autosomes
The 22 homologous pairs of chromosomes that code for all other genetic characteristics of the organism (not sex chromosomes).
Mutation
Changes to gene nucleotide sequences.
Mutagen
A factor that can increase the rates of mutations in cells (e.g., radiation, chemicals, carcinogens).
Replication
The process of copying DNA in the nucleus before a cell divides. Each DNA strand is copied exactly, creating 2 identical copies of the DNA double helix from the 1 original strand.
Sister chromatids
Identical copies of a chromosome; these are 2 identical strands of DNA joined by a centromere.
Mitosis
A form of cell division in eukaryotic cells that produces 2 genetically identical daughter cells.
Meiosis
A form of cell division in eukaryotic cells that produces gametes (egg and sperm) that have half the number of chromosomes than the parent cell.
Cell cycle
Cell cycle is the set of events that results in the creation of 2 daughter cells from 1 parent cell.
Interphase
The time between cell division.
Prophase
The first stage of mitosis.
Metaphase
Chromosomes align along the metaphase plate of the cell.
Anaphase
Sister chromatids break apart and move towards the poles of the cell.
Telophase
The final stage of mitosis, chromosomes un-condense to the state prior to prophase.
Cytokinesis
The dividing of the cell with the 2 nuclei into 2 separate cells with 1 nucleus each.
Crossing over
Crossing over: exchange of segments between non-sister chromatids of homologous chromosomes occurred during Meiosis; contributes to genetic variation.
Independent Assortment
During Metaphase I, each pair of homologous chromosomes orientates itself independently of all other pairs; contributes to genetic variation.
Fertilisation
In sexual reproduction, fertilisation results in the fusion of gametes to produce a zygote.