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  2. Insertion (genetics) - Wikipedia

    en.wikipedia.org/wiki/Insertion_(genetics)

    Insertions can be particularly hazardous if they occur in an exon, the amino acid coding region of a gene. A frameshift mutation, an alteration in the normal reading frame of a gene, results if the number of inserted nucleotides is not divisible by three, i.e., the number of nucleotides per codon. Frameshift mutations will alter all the amino ...

  3. Frameshift mutation - Wikipedia

    en.wikipedia.org/wiki/Frameshift_mutation

    Hypertrophic cardiomyopathy is the most common cause of sudden death in young people, including trained athletes, and is caused by mutations in genes encoding proteins of the cardiac sarcomere. Mutations in the Troponin C gene are a rare genetic cause of hypertrophic cardiomyopathy. A recent study has indicated that a frameshift mutation (c ...

  4. Slipped strand mispairing - Wikipedia

    en.wikipedia.org/wiki/Slipped_strand_mispairing

    This expands the replication region with newly inserted nucleotides. The template and the daughter strand can no longer pair correctly. [4] Nucleotide excision repair proteins are mobilized to this area where one likely outcome is the expansion of nucleotides in the template strand while the other is the absence of nucleotides.

  5. DNA repair - Wikipedia

    en.wikipedia.org/wiki/DNA_repair

    A cell that has accumulated a large amount of DNA damage or can no longer effectively repair its DNA may enter one of three possible states: an irreversible state of dormancy, known as senescence; cell suicide, also known as apoptosis or programmed cell death; unregulated cell division, which can lead to the formation of a tumor that is cancerous

  6. Gene duplication - Wikipedia

    en.wikipedia.org/wiki/Gene_duplication

    If an ancestral gene is pleiotropic and performs two functions, often neither one of these two functions can be changed without affecting the other function. In this way, partitioning the ancestral functions into two separate genes can allow for adaptive specialization of subfunctions, thereby providing an adaptive benefit.

  7. Crick, Brenner et al. experiment - Wikipedia

    en.wikipedia.org/wiki/Crick,_Brenner_et_al...

    The Crick, Brenner et al. experiment (1961) was a scientific experiment performed by Francis Crick, Sydney Brenner, Leslie Barnett and R.J. Watts-Tobin. It was a key experiment in the development of what is now known as molecular biology and led to a publication entitled "The General Nature of the Genetic Code for Proteins" and according to the historian of Science Horace Judson is "regarded ...

  8. Transposons as a genetic tool - Wikipedia

    en.wikipedia.org/wiki/Transposons_as_a_genetic_tool

    When additional nucleotides are inserted near or into a locus, the locus can suffer a frameshift mutation that could prevent it from being properly expressed into polypeptide chain. Transposon-based Insertional inactivation is considered for medical research from suppression of antibiotic resistance in bacteria to the treatment of genetic ...

  9. Copy number variation - Wikipedia

    en.wikipedia.org/wiki/Copy_number_variation

    In addition, if these trinucleotide repeats are in the same reading frame in the coding portion of a gene, it may lead to a long chain of the same amino acid, possibly creating protein aggregates in the cell, [7] and if these short repeats fall into the non-coding portion of the gene, it may affect gene expression and regulation. On the other ...

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