Meiosis/mutation Flashcards

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1
Q

Codon def

A

a sequence of three nucleotides which together form a unit of genetic code

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2
Q

What do gene mutations involves?

A

-a change in the base sequence of chromosomes

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3
Q

when can gene mutations arise?

A

-spontaneously during DNA replication

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4
Q

Describe base substitution

A

-Base substitution
> a nucleotide in a DNA molecule is replaced by another nucleotide which has a different base

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5
Q

what are two possible consequences of a base substitution?

A

> the a/a coded for may be changed which could affect a protein ( see protein topic )
however, new triplet of bases may still code for same a/a due to degenerate nature of genetic code, in which most a/a have more than one codon

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6
Q

Describe base deletion + consequence

A

-A nucleotide is lost from the normal DNA sequence
-a/a sequence of polypeptide completely different as one deleted nucleotide causes all triplets in a sequence to be read differently as they are shifted to the left

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7
Q

What can increase the rate of mutation

A

mutagenic agents

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8
Q

When can mutations in the number of chromosomes arise

A

spontaneously by chromosome non-disjunction during meiosis

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9
Q

How to calculate the number of different diiferent combinations of chromosomes following meiosis, without crossing over?

A

2 to the power of n, where n=number of homologous chromosome pairs

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10
Q

What does meiosis produce?

A

-daughter cells that are genetically different from each other

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11
Q

What is the first stage of meiosis ?

A
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12
Q

What are three differences between meiosis and mitosis

A

-Mitosis produces cells with the same number of chromosomes as the parent cell, whereas meiosis produces cells with half the number of chromosomes as the parent cell
-Mitosis produces daughter cells that are genetically identical, meisosis produces daughter cells that are genetically different from each other and parent cell
-mitosis produces 2 daughter cells, meiosis produces four

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13
Q

When would meiosis occur in an organisms life cycle?

A

-before sexual reproduction, as meiosis produces gametes which have half the number of chromosomes of the parent cell

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14
Q

How does random fertilisation of haploid gametes further increase genetic variation within a species?

A

-as it creates genetic variation between zygotes (cell formed by the fusion of male and female gametes) as each will have a unique combination of alleles

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15
Q

haploid def

A

A cell which has half of the usual complete set of chromosomes

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16
Q

diploid def

A

A cell with a complete set of chromosomes

17
Q

What are the two stages prior to meiosis

A

-before meiosis, DNA unravels and replicates so there are two copies of each chromosome, chromatids
-The DNA condenses to form double armed chromosomes, called centromeres, each made of 2 sister chromatids, joined together by a centromere

18
Q

Describe meiosis 1 and the stage immediately after in terms of the chromosome content of cells

A

-Meiosis 1(first division), the chromosomes arrange themselves at random into homologous pairs
-these homologous pairs are then seperated, halving the chromosome number

19
Q

Describe meiosis 2, and the step immediately after in terms of the chromosome content of the cells

A

-Meiosis 2 (second division), the pairs of sister chromatids that make up each chromosome are seperated ( the centromere is divided)
-four haploid cells (gametes) that are genetically different from each other are produced

20
Q

gene

A

a length of DNA that codes for a polypeptide

21
Q

locus

A

the posistion of a gene on a chromosome or DNA molecule

22
Q

allele

A

one of the different forms of a particular gene

23
Q

homologous chromosome

A

a pair of chromosomes, one of maternal and one of paternal, that have the same gene loci

24
Q

Describe the independent segregation of of homologous chromosomes

A

-In meiosis 1 (first division) the chromosomes arrange themselves at random into homologous pairs
-one of each of these pairs will go to each daughter cell (depending on how the chromosomes are lined up)
-seeing as the pairs are lined up at random, the combination of chromosomes of maternal and paternal origin that goes into a daughter cell at meiosis 1 is also a matter of chance
-this is called independent segregation

25
Q

How does the independent segregation of homologous chromosomes result in genetic variation?

A

-each member of a homologous pair having the same genes and therefore determining the same characteristics
-but the alleles of these genes may differ
-the independent segregation of these chromosomes therefore results in new genetic combinations

26
Q

Describe the process of crossing over between homologous chromosomes and how it leads to further genetic variation among daughter cells.

A

-Meiosis 1(first division), the chromosomes arrange themselves at random into homologous pairs then:
>The chromatids of each pair become twisted around each other
> During this, tensions are created and portions of the chromatids break off
>these broken portions might rejoin with the chromatids of their homologous partner
> Usually it is the equivalent portions of homologous chromosomes that are exchanged
-in this way, genetic combinations of maternal and paternal alleles are produces
-