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December 19, 2017 Journal: What is the difference between how nucleotides are added to the leading and lagging strands in DNA replication?
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Mutations, Chromosomes, and Karyotypes
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Eukaryotic Chromosomes
Made of DNA and protein Function is to pass on traits
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When a cell is not dividing, chromosomes are long, thin strands
Before division, they get short & thick and form chromosomes
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Each organism has a characteristic # of chromosomes
Ex. Humans have 46 chromosomes Sexually reproducing organisms have 2 sets with same type of genetic info
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Arranged in a karyotype that shows all our 46 chromosomes as 23 pairs
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Genes: Sections of chromosomes
Vocabulary Genes: Sections of chromosomes Chromatin: DNA + Proteins that make up chromosomes Centromere: The middle of the chromosome that holds the two sister chromatids together
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Genes are Sections of Chromosomes
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Mutations involve Changes in DNA
May be caused by environmental factors called mutagens
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Chromosome mutations – affect whole chromosome
Mutations may be Chromosome mutations – affect whole chromosome Ex. Trisomy 21 aka Down Syndrome Gene mutations – affect a single gene
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Types of gene mutations
Substitution - Substitute 1 nucleotide base for another Insertion - Add one or more extra nucleotides Deletion- Remove 1 or more nucleotides
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Substitutions are known as point mutations
Possibly change 1 amino acid May be “silent” May introduce stop codon Insertion/Deletion result in Frameshift Can change the whole reading frame of the mRNA
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Mutations may be Helpful Harmful Neutral
Give organism new trait beneficial to their survival Harmful Make them less likely to survive Neutral No affect
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Evolution Link: Mutations are the ultimate source of variation
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