topic 1 Flashcards

1
Q

whats a function of the non-conding dna in the genome

A

they regulate transcription

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2
Q

genome

A

total genetic material present in an organism

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3
Q

what is a genome made of

A

made up of genes (coding regions) and other DNA sequences that do not code for a protein (non-coding regions)

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4
Q

whats the repeated strand in a dna

A

nucleotide - sugar base phosphate

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5
Q

whats a dna nucleotide made of

A

deoxyribose sugar, phosphate, base

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6
Q

what carbon does the base attach to

A

carbon 1

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7
Q

whats the backbone of a dna made of

A

the phosphate of one nucleotide and the carbon 3 of another , joined by strong chemical bonds

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8
Q

what holds the bases together

A

weak hydrogen bonds

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9
Q

what is needed for the leading strand during pcr

A

dna polymerase , primer

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10
Q

what does a lagging strand need during pcr and why

A

needs primer, its a short strand of nucleotides to start the dna replication
needs dna polymerase to add dna nucleotides
ligase is needed to put the fragments together

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11
Q

how does PCR happen

A
  • heated to 95, hydrogen bonds break, dna unzips
  • cooled to 55 allows primers to bind to their specific target sequences at the 3’ end
  • heaed to 75, allows the heat tolerant dna polymerase to replicate the original dna
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12
Q

what is gene expression

A

is the activation of certain genes in a cell to produce a particular proteins, only a fraction of the genes in a cell are expressed

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13
Q

whats an rna made of

A

single stranded
made of nucleotide
ribose sugar, phosphate, base

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14
Q

mRNA

A

it carries a copy of the DNA code from the nucleus to ribosome

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15
Q

what r the rna bases

A

uracil-adenine
cytosine - guanine

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16
Q

tRNA

A

found in cytoplasm
binds to specific amino acids and transports them to ribosome

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17
Q

rRNA

A

forms a complex with protein molecules to make the ribosome

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18
Q

what happens during transcription

A

-rna polymerase moves along and unwinds double helix
rna polymerase synthesises a primary transcript of mrna from rna nucleotides by complementary base pairing
they pair up
and rna splicing occurs

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19
Q

codon

A

a triplet of three bases on mRNA each codes for a specific amino acid

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20
Q

what happens in translation

A

begins at mRNA start and stop codon
tRNA brings specific amino acids
the tRNA anti codons bind by complementary base pairing
peptide bonds join amino acid together
tRNA leaves

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21
Q

alternative rna splicing

A

happens when a different mature mRNA transcript is produced by the same primary transcript depending on which exons r retained

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22
Q

polypeptide structure

A

amino acids bonded by peptide bonds
three dimensial shape
held by hydrogen bonds

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23
Q

cellular differentiation

A

the process by which a cell expresses certain genes to produce proteins characteristics for that type of cell.
this allows a cell to carry out specialised functions

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24
Q

meristem cells

A

unspecialised cells in plants

25
Q

embroyonic stem cells

A

pluripotent

26
Q

tissue stem cells

A

multipotent can only differentiate into a cell related to tissue/muscle

27
Q

mutations definition

A

mutations are changes to the dna
they arise spontaneously and at random but occur rarely

28
Q

what is substitution mutation

A

single nucleotide substitution which can bring about only a minor change

29
Q

what are the three types of substitution mutations

A

missense - little affect
nonsense - amino acids becomes into a stop codon, causes it to form a shorter polypeptide chain
splice site - results in some introns being retained or some exons been taken out

30
Q

insertion definition

A

an extra nucleotide is added into the sequence
this alters all the codons

31
Q

deletion definition

A

a nucleotide is removed from the sequence this alters al the codons

32
Q

what mutation is classified as a frame-shift mutations

A

insertion and deletion as it alters all the amino acids from the mutation and onwards

33
Q

what are the 4 types of chromosome mutations

A

involves the chromosome structure being altered
deletion
duplication
translocation
inversion

34
Q

what is deletion chromosome structure mutation

A

a section of chromosome is removed

35
Q

what is duplication chromosome structure mutation

A

a section of a chromosome is added from its homologous partner

36
Q

what is translocation chromosome structure mutation

A

a section of chromosome is added from its non homologous partner

37
Q

what is inversion chromosome structure mutation

A

a section of chromosome is reversed within itself

38
Q

what is evolution

A

evolution is the change that occurs in organisms over generations as a result of genomic variation.
these variations take the form of changes in the frequencies of certain genetic sequences

39
Q

vertical inheritance

A

genes are transferred from parent to offspring as a result of sexual or a sexual reproduction

40
Q

horizontal inheritance

A

genes are transferred between individuals in the same generations
prokaryotic can transfer genetic materical (plasmids) from one cell to another horizontally

41
Q

natural selection

A

is the non-random increase in frequency of DNA sequences that increase survival and the non-random reduction in deleterious (harmful) sequences

42
Q

what are the types of selections that can occur for a quantitative trait

A

stabilising selection
directional selection
disruptive selection

43
Q

whats a quantitative trait

A

a quantitative trait is polygenic, it is controlled by many genes working together

44
Q

species definition

A

is a group of organisms that are able to interbreed with one another to produce fertile offspring

45
Q

speciation

A

is the formation of a new species bought about by evolution as a result of isolation, mutation and selection

46
Q

what is allopatric speciation

A

population becomes separate by a geographical barrier

47
Q

what is a sympatric speciation

A

when 2 populations live in the same environment but become isolation due to behavioural or ecological barriers

48
Q

genomic sequencing

A

is the sequence of nucleotide bases can be determined for an individual and entire genomes

49
Q

bioinformatics

A

are computer programs that can be used to identify base sequences by looking for a sequences and similar to known genes

50
Q

phylogenetics

A

is the study of evolutionary history and relationships

51
Q

molecular clocks

A

molecular clocks are used to show when species diverged during evolution

52
Q

what are the three domains of life

A

bacteria
archaea
eukaryotes (fungi plants n animals)

53
Q

pharmacogenetics

A

is the use of genome information in the choice of drugs it could lead to personalised medication

54
Q

suggest how a change in the sequence
of bases in DNA transcribed to rRNA in the mutated cultures resulted in a
decrease in protein synthesis.

A

Change in the sequence may change
the structure/function/shape of the
ribosome
Translation can no longer occur

55
Q

A molecular clock was used to estimate the dates of the divergence of
each species.
Give one example of the type of data required to generate a molecular
clock.

A

-mutation rate
-dna sequence data
-fossils

56
Q

species

A

is a group of organism that can produce off spring

58
Q

when comparing genomic sequence data, bioinformatics is the use of

A

computer analysis, and statistical anaylsis