4 Genetic Information & variation- Mutations & meiosis Flashcards

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1
Q

What are mutations?

A

Changes to the base sequence of DNA
Almost always harmful- interrupt normal functioning of a protein

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2
Q

What causes mutations?

A

Addition,deletion and substitution of bases

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3
Q

What is an addition mutation?

A

Where one or more bases are added to the DNA sequence
e.g. ATCGTT—> ATCCGTT

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4
Q

What is a deletion mutation?

A

Where one or more bases are removed from the DNA sequence
e.g. ATCGTT—> ATCTT

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5
Q

What is a substitution mutation?

A

Where one or more bases are changed in the DNA sequence
e.g. ATCGTT—> ACCGTT

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6
Q

What processes cause gene mutations?

A

DNA replication
-Bases in DNA sequence are read & copied; can be errors in replication process, causing mutation, which are spontaneous
Mutagenic agents
-Increase rate of gene mutations. Include chemicals, e.g bromine, and exposure to ionising and ultraviolet radiation
Chromosome mutation
-Arise spontaneously during meiosis, affect number of chromosomes in developing zygote (aneuploidy) Non-disjunction= chromosomes don’t separate properlyi

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7
Q

What is meiosis and its role?

A

The process that produces haploid (half number of chromosomes) gamete cells from diploid (full amount of chromosomes) cells. It is necessary for sexual reproduction to take place; gametes fusing together to make a new diploid organism, one copy of chromosome from each parent

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8
Q

How is meiosis genetically diverse?

A

-Makes 4 genetically diverse daughter cells, which receive different combination of chromosomes
-Random fertilisation means that any 2 gametes can fuse together to produce a random combination of chromosomes

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9
Q

What happens in the first stages of meiosis?

A

-Chromosomes in cells replicate, produce identical copy of each other- chromatids. These condense to form a double-armed chromosomes; each arm made from one chromatid and joined by a centromere, called sister chromatids
-Chromosomes are found in homologous pairs (chromosomes w/ identical genes, different alleles). They’re arranged in the centre of a cell, moved by spindle fibres
-Homologous chromosomes separate, pulled to opposite ends of cell by spindle fibres; the separation from each pair is random, and they’re pulled to each side of cell

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10
Q

What happens during cell division (meiosis I)?

A

-As homologous chromosomes separate, cell divides into two cells
-One chromosome from each pair is separated into each cell
-This is meiosis I, and produces 2 genetically different daughter cells
-Sister chromatids separated randomly by spindle fibres, pulled to opposite ends of cell

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11
Q

What happens during the 2nd cell division (meiosis II)?

A
  • As sister chromatids separate, cell divides into 2 new cells.
    -One chromatid from a chromosomes is separated into each cell; this is meiosis II
    -Produces four genetically different haploid cells
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12
Q

What are the 2 ways in which meiosis creates genetic variation?

A

Crossing over & independent segregation

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13
Q

What is crossing over?

A

-Chromosomes of a homologous pair are arranged down the middle of a cell before first division in meiosis I
-Sections of DNA are swapped between chromosomes in a pair; this is crossing over
-Produces new combinations of alleles; a key part of genetic recombination
-Increases genetic variation

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14
Q

What is independent segregation?

A

The process of separating chromosomes into random combinations
-Chromosomes in homologous pair are separated in meiosis I in random formation, producing 2 genetically different daughter cells
-Increases genetic variation

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15
Q

What is the difference between meiosis and mitosis?

A

Number of cells
-Meiosis; 4, mitosis; 2
Number of chromosomes
-Meiosis; haploid, 23 (half of parent cell), mitosis; diploid, 46
Genetic variation
-Meiosis; genetically different daughter cells, mitosis; genetically identical daughter cells
Products
-Meiosis; gametes only, Mitosis; replication of every body cell

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