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Nucleic acids (RNA and DNA) are polymers formed when nucleotides join by phosphodiester bonds. Nucleotides have three components: a phosphate group, a pentose sugar and a nitrogenous base.
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DNA undergoes semi-conservative replication. During replication, errors may occur through transition, transversion or strand slippage. Both transition and transversion lead to single nucleotide polymorphisms (SNPs).
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Protein synthesis is a multi-stage process (transcription; splicing; amino acid activation; translation; post-translational modification) requiring both DNA and RNA. DNA is the molecular code which determines the types and sequence of amino acids within a protein. RNA is crucial to the assembly of proteins.
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The cell cycle is a multi-stage process during which the cell increases in size (G1), replicates its DNA (S), prepares to divide (G2) and then divides (M). The cell cycle is regulated by cyclin-dependent kinases (CDKs) and negative regulatory molecules, whose actions create three main checkpoints in the cell cycle: G1 (restriction) checkpoint; G2 checkpoint and metaphase checkpoint.
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During mitotic cell division, which can be subdivided into prophase, metaphase, anaphase and telophase, identical copies of genes are passed to diploid (2n) daughter cells.
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Daughter cells formed during meiosis, which takes place during gametogenesis, are not genetically identical and are haploid (n). Meiosis, which is also known as reduction division, has two main phases: meiosis I (reduction) and meiosis II (division). In humans, spermatogenesis takes place in the testes and oogenesis takes place in the ovaries. Haploid (n) gametes fuse during fertilisation to form a diploid (2n) zygote.
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Genetic information is passed to the next generation in the form of alleles, which are variant forms of genes. Inheriting two identical alleles leads to a homozygous genotype whereas inheriting different alleles leads to a heterozygous genotype. The resulting phenotype depends on whether alleles are dominant, codominant or recessive. The Chi-squared test can be used to assess whether the observed outcome of a genetic cross matches the expected ratio.
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The genome is the genetic information of an organism. The genome includes coding (exons) and non-coding (introns and intergenic DNA) regions, as well as mitochondrial DNA. Genomes can be modified using gene technologies; products of genetically modified organisms (GMOs) are used in medicine, agriculture and industry.
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