Zusammenfassung der Ressource
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Mutations are a change in an organisms [blank_start]DNA[blank_end]. DNA mutations can result in a change in protein structure or not, these are referred to as non-[blank_start]synonymous[blank_end] and [blank_start]synonymous[blank_end] mutations respectively. Mutations can involve the [blank_start]substitution[blank_end] of one base for another, or the [blank_start]deletion[blank_end]/[blank_start]insertion[blank_end] of a base.
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DNA
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synonymous
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synonymous
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substitution
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deletion
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insertion
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The reading frame of a piece of DNA determines which [blank_start]amino[blank_end] acids are assembled into a [blank_start]protein[blank_end] molecule. Insertions and deletions can cause [blank_start]frame[blank_end] shifts, [blank_start]changing[blank_end] the codons downstream of the mutation.
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amino
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protein
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frame
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changing
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Mutations are responsible for over 4000 [blank_start]genetic[blank_end] diseases in humans. Some of these diseases stem from just a single [blank_start]nucleotide[blank_end] mutation. One example of this is in cystic [blank_start]fibrosis[blank_end], which is caused by mutation of the gene encoding the CFTR protein. One of the most well known genetic diseases worldwide is [blank_start]cancer[blank_end].
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genetic
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nucleotide
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fibrosis
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cancer
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Cancer is caused by cells losing their ability to control cell [blank_start]division[blank_end], to undergo programmed cell [blank_start]death[blank_end] and many other hallmarks. Cancer progression occurs following a sequence of [blank_start]mutations[blank_end] in [blank_start]tumour[blank_end] [blank_start]suppressor[blank_end] [blank_start]genes[blank_end] and proto-[blank_start]oncogenes[blank_end].
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division
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death
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mutations
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tumour
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suppressor
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genes
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oncogenes
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Appropriately label the diagram below
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The likely hood of cancer is increased if you are exposed to [blank_start]mutagens[blank_end]. This is because mutagens increase the [blank_start]mutation[blank_end] [blank_start]rate[blank_end] of your cells.