Genes and Inheritance Flashcards

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1
Q

Genome Definition:

A

All of the DNA found in an organism

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2
Q

Gene Definition:

A

A section of a molecule of DNA that codes for a specific protein

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3
Q

Where are genes located

A

On chromosomes in the nucleus

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4
Q

DNA structure

A

Double helix (2 strands)
Bases paired up (complementary base pairing) A-T, C-G

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5
Q

RNA structure

A

Single strand
A-U, C-G

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6
Q

Nucleotide made up of:

A

Phosphate
Sugar (Ribose/Deoxyribose)
Nitrogenous Base

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7
Q

5 types of bases

A

Adenine
Thymine (DNA)
Cytosine
Guanine
Uracil (RNA)

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8
Q

Codon/Anticodon

A

Triplet of (unpaired) bases

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9
Q

Transcription (nucleus)

A

Occurs in Nucleus
-Part of DNA unwinds, bonds between base pairs break
-Template strand exposed: ONLY ONE STRAND
-Free mRNA nucleotides in nucleus bind to complementary nucleotides
-mRNA nucleotides join together, forming mRNA strand
-mRNA leaves the nucleus via nuclear pore
-mRNA complementary copy of DNA code from original gene

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10
Q

Translation (cytoplasm)

A

Occurs in ribosomes
-mRNA attaches to ribosome
-Free tRNA molecules in cytoplasm have anticodons on one end, amino acid on the other
! - each specific anticodon corresponds to a specific amino acid
-The anticodon (tRNA) pairs to its complementary codon (mRNA)
-This repeats and peptide bonds are formed between AAs
-This continues until a ‘stop’ codon is reached on mRNA
-Amino acid chain folds to form protein

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11
Q

Why is RNA needed

A

DNA cannot leave the nucleus as it is a big molecule

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12
Q

Alleles Definition:

A

Variations of the same gene
e.g. blue/black eyes

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13
Q

Dominant Allele (A):

A

Allele that is always expressed

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14
Q

Recessive Allele (a):

A

Allele that is expressed only when there is no dominant allele

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15
Q

Homozygous and Heterozygous:

A

Both alleles are the same vs
Both alleles are different

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16
Q

Genotype and Phenotype

A

G: Alleles for a particular characteristic
Ph: Physical appearance caused by alleles

17
Q

Co-dominance

A

When neither allele is dominant, both are expressed in phenotype

18
Q

Polygenic Inheritance definition:

A

When 2 or more genes work together to control a characteristic

19
Q

Male Female genotype

A

XY, XX

20
Q

Diploid Definition

A

Cell containing 2 sets of chromosomes

21
Q

Mitosis (IPMAT)

A

-Produces diploid cells, identical to parent cell
Interphase: DNA in chromosomes replicate themselves for mitosis
Prophase: Chromatids condense and become visible, and nuclear membrane disappears
Metaphase: Spindle forms, chromatids line up in middle
Spindle attaches to their centromeres
Anaphase: Spindle fibres shorten and pull chromatids to poles, separating them
Telophase: New membrane form around chromosomes at each end of cells, forming 2 new nuclei. Cytoplasm divides to form 2 daughter cells that are diploid

22
Q

Meiosis

A

-Produces 4 genetically different haploid cells
Cells divide twice (IPMAT x 2)
Metaphase 1: Maternal and Paternal Chromosomes pair up along center but are not separated
Metaphase 2: Same as mitosis, seperated
All daughter cells are haploid

23
Q

Homologous Chromosome Definition:

A

Matching (but unidentical) pairs of a chromosome

24
Q

Mitosis vs Meiosis

A

2 cells prod. vs 4 cells prod.
diploid vs haploid
genetically identical vs different

25
Q

Mutation definition:

A

A random process in genes or chromosomes that changes a DNA sequence

26
Q

Insertion:

A

Extra nucleotide added
Frameshift mutation - whole amino acid sequence from this point onwards changes as each triple after is now different (every codon shifts)

27
Q

Deletion

A

Nucleotide deleted
Frameshift mutation - whole amino acid sequence from this point onwards changes

28
Q

Substitution

A

Different nucleotide used
Triplet of bases in which mutation occurs changes
Rest of the chain unaffected
! - new triplet could still code for same amino acid (AAs have more than one code)

29
Q

Inversion

A

Order of bases in a triplet is reversed e.g CCT -> TCC
Similar effects to substitution

30
Q

How can mutations be passed on to offspring?

A

Mutation in gametes

31
Q

Increases in risk of mutation

A

Mutagens:
Ionising radiation - Gamma, X-rays, UV
Chemicals in cigarettes, mustard gas, nitrous oxide, benzenes