diversity and selection (p1) Flashcards

include meiosis and mutations

1
Q

diploid body cells

A

normal body cells have a diploid number of chromosomes (2n). two of each chromosome one from mum and one from dad. .

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2
Q

Gene __________ involve a change in the base sequence of
chromosomes. They can arise spontaneously during DNA
__________ and include base deletion and base substitution. Due to
the ______ nature of the genetic code, not all base
substitutions cause a change in the sequence of encoded amino
acids.___________ agents can increase the rate of gene mutation.

A

Gene mutations involve a change in the base sequence of
chromosomes. They can arise spontaneously during DNA
replication and include base deletion and base substitution. Due to
the degenerate nature of the genetic code, not all base
substitutions cause a change in the sequence of encoded amino
acids. Mutagenic agents can increase the rate of gene mutation.

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3
Q

Mutations in the number of chromosomes can arise spontaneously
by chromosome ______-__________ during meiosis.

A

Mutations in the number of chromosomes can arise spontaneously
by chromosome non-disjunction during meiosis.

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4
Q

Meiosis produces daughter cells that are genetically __________ from
each other.

A

Meiosis produces daughter cells that are genetically different from
each other.

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5
Q

The process of meiosis only in sufficient detail to show how:
*_____ nuclear divisions result usually in the formation of four
_________ daughter cells from a single diploid parent cell
* genetically _________ daughter cells result from the
independent _________ of homologous chromosomes
* ________over between homologous chromosomes results in
further genetic variation among daughter cells

A

The process of meiosis only in sufficient detail to show how:
* two nuclear divisions result usually in the formation of four
haploid daughter cells from a single diploid parent cell
* genetically different daughter cells result from the
independent segregation of homologous chromosomes
* crossing over between homologous chromosomes results in
further genetic variation among daughter cells

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6
Q

homologous pairs

A

chromosomes that make up a pair are same size and have same genes although may have different alleles these pairs of matching chromosomes are homologous pairs

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7
Q

gametes

A

sperm cells in males egg cells in females. have a haploid number of chromosome (n). one copy of each chromosome . Haploid number in humans is 23.

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8
Q

in sexual reproduction 2 gametes fuse together to form a ______ which divides and develops into a new organism

A

in sexual reproduction 2 gametes fuse together to form a zygote which divides and develops into a new organism

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9
Q

at fertilisation ______ sperm fuses with ______ egg forming a cell with a diploid number of chromosomes. Half from father half from mother

A

at fertilisation haploid sperm fuses with haploid egg forming a cell with a diploid number of chromosomes. Half from father half from mother

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10
Q

during sexual reproduction any sperm can fuse with any egg (its ________). It produces zygotes with a random combination of chromosomes from the parents .mixing of genetic material in sexual reproduction increases genetic _________ within a species.

A

during sexual reproduction any sperm can fuse with any egg (its random). It produces zygotes with a random combination of chromosomes from the parents .mixing of genetic material in sexual reproduction increases genetic diversity within a species.

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11
Q

meiosis vs mitosis

A

meiosis: produces haploid cells, daughter cells genetically different from eachother and parent cell,produces 4 daughter cells
mitosis:produce diploid cell, daughter cells are genetically identical to each other and the parent cell,produces 2 daughter cells

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12
Q

meiosis

A

1.before meiosis starts DNA replicates, forming 2 copies of each chromosome called chromatids
2.DNA condenses to form a double armed chromosome,made of two sister chromatids, that are joined by a centromere.
3.Meiosis I-chromosomes arranged themselves in homologous pairs
4. these homologous pairs are then separated halving the chromosome number.
5.meiosis II-pair of sister chromotids that make up a pair are separated (centromere is divided.)
6.2 haploid cells that are genetically different are produced

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13
Q

what happens in first meiotic division

A

chiasmata are formed (cross overs)
gamete mother cell is present
homologous chromosomes form pairs

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14
Q

what happens in the second meiotic division

A

haploid gametes are produces
chromatids separate

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15
Q

what 2 main events during meiosis lead to genetic variation

A

1.crossing over of chromatids
2. independent segregation of chromosomes.

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16
Q

crossing over of chromatids

A

.during meiosis I chromosomes come together and pair up. the chromatids twist around eachother and bits of the chromatids swap over
.chromatids still contain the same genes but a different combination of alleles.
.means each of the 4 daughter cell produced in meiosis II contain chromatids with different alleles.

17
Q

dependant segregation of chromosomes.

A

-each homologous pair is made from one chromosome from mum and one from dad
-when homologous pairs are separated in meiosis I it is completely random what chromosome ends up in what daughter cell
-so each each of the 4 daughter cells produced in meiosis have completely combinations of maternal and paternal chromosomes.
-this is independent segregation of chromosomes
-this shuffling of chromosomes leads to genetic variation in any potential offspring

18
Q

Gene mutations

A

invlove a change in the DNA base sequence of chromosomes and include
substitution,deltion,addition,duplication,inversion and translocation.
order of DNA bases in a gene determines the order of amino acids in particular protein. if a mutation occurs in a gene it can effect the amino acid it codes for

19
Q

substitution

A

one base substituted with another

20
Q

deletion

A

one or more bases are deleted

21
Q

what can cause DNA mutations

A

errors in DNA replication

22
Q

addition

A

one or more bases are added.

23
Q

duplication

A

one or more bases are repeated

24
Q

inversion

A

sequence of bases are reversed

25
translocation
sequence of bases is removed from one location in the genome to another . it could be within the same chromosome or a different chromosome.
26
effects of genetic mutation
-due to genetic codes degenerate nature , some amino acids are coded for by more than one DNA triplet -some substitution reactions won't result in a change in the amino acid sequence- as they may code for the same amino acid -but deltions will effect order of amino acids as it will change the number of bases presnt which will cuase a shift in all the base triplets after it
27
frameshift mutations
-some mutations have a huge effect on base sequence of a gene -additions/duplication and deletions within a gene almost certainly change the amino acid sequence within a polypeptide -because the mutations change the number of bases in the DNA code -resulting in a frameshift in base triplets,so triplet code is read in a different way.
28
mutagenic agents
increase the rate of mutations mutations occur spontaneously e.g when DNA is misread in DNA replication, but somethings increase the rate of mutations-mutagenic agents. for example UV ,ionsiing radiation some chemicals and some viruses. they increasing the probability of a mutation occuring
29
effects of mutagenic agents
-acting as a base :chemicals called base analogs can substitute for bases during DNA replication changing base sequnce of new DNA -changing DNA structure: some types of radiation can change the stucture of DNA causing problems in DNA replication -altering bases:some chemicals can delete or alter bases
30
chromosome mutations
-sometimes meiosis goes wrong and cells produced contain variations in the number of chromosomes or parts of chromosomes -can lead to inherited conditions because the errors are present in the gametes -one type of chromosome mutation is chromosome non-disjunction
31
chromosome non-disjunction
failure of chromosome to separate properly