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Genetics (Mutations (Point mutations (chemical changes in just one…
Genetics
Mutations
Silent mutation
a change in a nucleotide pair transforms one codon into another that is translated into the same amino acid.
Point mutations
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f a point mutation occurs in a gamete or in a cell that produces gametes, it may be transmitted to future generations.
If the mutation has an adverse effect on the phenotype of an organism, the mutant condition is referred to as a genetic disorder or hereditary disease.
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Nonsense mutation
change an amino acid codon into a stop codon, causing premature termination of translation and nearly always leading to a nonfunctional protein.
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Translation
Steps
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Each time a new tRNA comes into the ribosome, the amino acid that it was carrying gets added to the elongating polypeptide chain.
The ribosome continues until it hits a stop sequence, then it releases the polypeptide and the mRNA.
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Types of RNA
mRNA
messenger RNA is a copy of a gene. It acts as a photocopy of a gene by having a sequence complementary to one strand of the DNA and identical to the other strand. The mRNA acts as a busboy to carry the information stored in the DNA in the nucleus to the cytoplasm where the ribosomes can make it into protein.
tRNA
transfer RNA is a small RNA that has a very specific secondary and tertiary structure such that it can bind an amino acid at one end, and mRNA at the other end. It acts as an adaptor to carry the amino acid elements of a protein to the appropriate place as coded for by the mRNA.
rRNA
ribosomal RNA is one of the structural components of the ribosome. Its sequence is the compliment of regions in the mRNA so that the ribosome can match with and bind to an mRNA it will make a protein from.
RNA splicing
The most remarkable stage of RNA processing occurs during the removal of a large portion of the RNA molecule in a cut-and-paste job of RNA splicing.
RNA splicing removes introns and joins exons to create an mRNA molecule with a continuous coding sequence.
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Polyribosomes
single mRNA may be used to make many copies of a polypeptide simultaneously as multiple ribosomes, polyribosomes or polysomes, trail along the same mRNA.
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Replication
DNA Structure
double helix
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the two sugar-phosphate backbones are antiparallel, with the subunits running in opposite directions.
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DNA replication
Prokaryotes
in the prokaryotic bacterium E. coli, replication can occur at a rate of 1,000 nucleotides per second.
Eukaryotes
in comparison, eukaryotic human DNA replicates at a rate of 50 nucleotides per second.
Steps
Step 3
After the primer is in place on a single, unwound polynucleotide strand, DNA polymerase wraps itself around that strand, and it attaches new nucleotides to the exposed nitrogenous bases.
Beginning at the primer sequence, DNA polymerase (shown in blue) attaches to the original DNA strand and begins assembling a new, complementary strand.
Step 4
As DNA polymerase makes its way down the unwound DNA strand, it relies upon the pool of free-floating nucleotides surrounding the existing strand to build the new strand.
The nucleotides that make up the new strand are paired with partner nucleotides in the template strand; because of their molecular structures, A and T nucleotides always pair with one another, and C and G nucleotides always pair with one another.
This phenomenon is known as complementary base pairing, and it results in the production of two complementary strands of DNA.
Step 2
Meanwhile, as the helicase separates the strands, another enzyme called primase briefly attaches to each strand and assembles a foundation at which replication can begin.
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Step 5
A new DNA strand is synthesized. This strand contains nucleotides that are complementary to those in the template sequence.
Step 1
First, a so-called initiator protein unwinds a short stretch of the DNA double helix.
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Then, a protein known as helicase attaches to and breaks apart the hydrogen bonds between the bases on the DNA strands, thereby pulling apart the two strands, forming a replication “bubble.”
As the helicase moves along the DNA molecule, it continues breaking these hydrogen bonds and separating the two polynucleotide chains
Telomeres
The ends of eukaryotic chromosomal DNA molecules have special nucleotide sequences called telomeres.
Telomeres do not contain genes. Instead, the DNA typically consists of multiple repetitions of one short nucleotide sequence.
Telomeric DNA acts as a kind of buffer zone that protects the organism’s genes. Telomeres become shorter during every round of replication.
Transcription
Steps
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During this process, an adenine (A) in the DNA binds to an uracil (U) in the RNA.
the addition of nucleotides to the mRNA strand. RNA polymerase reads the unwound DNA strand and builds the mRNA molecule, using complementary base pairs.
the ending of transcription, and occurs when RNA polymerase crosses a stop (termination) sequence in the gene
The mRNA strand is complete, and it detaches from DNA.
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