intro to Molecular bio Flashcards

1
Q

what is molecular biology

A

field of science studying the chemical structures & processes that involve the basic units of life( molecules)

there are many molecules but the term is usually used to describe the study of nucleic acids

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2
Q

why study molecular biology

A

nucleic acids form the information of hereditary genes

the sequence of nucleotides is the basis for normal & pathological traits in all species

  • provides info to what is happening
  • provides info to predict what could happen
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3
Q

DNA

A

A nucleic acid that stores information
DNA is inherited

has a deoxyribose sugar, a phosphate group & base pairs ( adenine, tyrosine, guanine & cytosine)

usually double stranded

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4
Q

RNA

A

there are many types
- can serve as an intermediate for protein production ( coding RNA)
- can serve a direct biological function ( non coding RNA; ncRNA)
RNA is transcribed from DNA

has ribose sugar, a phosphate, & base pairs ( Adenine, uracil, guanine & cytosine )

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5
Q

gene

A

segment of DNA that encodes for a product with a biological function
- products are either proteins or RNA

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6
Q

meaning of an expressed gene

A

when the information in a gene has been used by the cell to make a gene product

“switched on “

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7
Q

amino acids

A

proteins are made up of amino acids

  • each amino acids is encoded by a triplet nucleotide code called a codon
  • the human genetic code compromises 64 codons which encode for 21 amino acids & 3 stop codons
  • mRNA codons are read by anticodon regions of transfer RNA ( tRNA)
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8
Q

tRNA

A

transfer RNA brings the corresponding amino acid to the growing polypeptide chain

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9
Q

ribosomes

A

the polypeptide chain is synthesized by ribosomes which are macromolecular complexes containing ribosomal RNA ( rRNA) & a protein component

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10
Q

transcription

A

taking information from a gene ( DNA) to an RNA molceule

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11
Q

Translation

A

info in the mRNA molecule is used to make a protein

  • mRNA sequence forms an amino acid sequence
  • occurs on the cytoplasmic ribosomes
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12
Q

Genome

A

complete set of chromosomes

total complement of hereditary information

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13
Q

genetic code

A

complete list of nucleotide codons & the amino acids or actions for which they “code”

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14
Q

human cells

A

contain 2 full copies of the haploid human genome organized into 23 pairs of chromosomes to form diploid genome

  • one full set of chromosomes is inherited from each parent
  • human genomes has 2 copies of each gene - terms alleles*
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15
Q

chromosome

A

highly ordered structure of a single DNA molecule with specialized structural features including one centromere & two telomeres

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16
Q

Allele

A

Alternative version of a gene at a given location ( locus) along a gene

  • you get 2 alleles of each gene ( one from each parent)
  • if the 2 alleles are the same, the individual is homozygous for that gene
  • if the 2 alleles are different, they are heterozygous for that gene
17
Q

Genotype

A

primary nucleotide sequence of the two gene alleles

genetic makeup - genotype codes for the phenotype

18
Q

Phenotype

A

expressed function of biological effect of the gene product

observable physical or biochemical characteristics of an individual

19
Q

Human disease - genotyping or phenotyping

A

human disease can be studied at the genetic level through determination of the allelic sequence of a gene by genotyping

or at the functional level by phenotyping
ex of phenotyping
- enzyme concentration or activity
- ABO blood groups
- electrophoretic mobility of hemoglobin variants
- RNA expression levels

choice of genotyping or phenotyping for making a diagnosis depends on the specific diagnostic application & the strength of association between a genotype & its sequential phenotype