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  2. Chromosomal inversion - Wikipedia

    en.wikipedia.org/wiki/Chromosomal_inversion

    An inversion is a chromosome rearrangement in which a segment of a chromosome becomes inverted within its original position. An inversion occurs when a chromosome undergoes a two breaks within the chromosomal arm, and the segment between the two breaks inserts itself in the opposite direction in the same chromosome arm.

  3. Structural variation in the human genome - Wikipedia

    en.wikipedia.org/wiki/Structural_variation_in...

    The products of this mechanism from the sequence repeats is depicted in Figure 2. A study was done on the olfactory receptor gene clusters where they questioned if there was an association between normal rearrangement of 8p and the repeated inverted sequences. The researchers observed that the rearrangement of chromosomes was actually caused by ...

  4. Gene conversion - Wikipedia

    en.wikipedia.org/wiki/Gene_conversion

    Biased gene conversion (BGC) occurs when one allele has a higher probability of being the donor than the other in a gene conversion event. For example, when a T:G mismatch occurs, it would be more or less likely to be corrected to a C:G pair than a T:A pair. This gives that allele a higher probability of transmission to the next generation.

  5. Molecular drive - Wikipedia

    en.wikipedia.org/wiki/Molecular_drive

    The mechanisms involved include gene conversion, unequal crossing-over, transposition, slippage replication and RNA-mediated exchanges. Because mutations changing the sequence of one copy are less common than deletions , duplications and replacement of one copy by another, the copies gradually come to resemble each other much more than they ...

  6. Fusion gene - Wikipedia

    en.wikipedia.org/wiki/Fusion_gene

    The first fusion gene [1] was described in cancer cells in the early 1980s. The finding was based on the discovery in 1960 by Peter Nowell and David Hungerford in Philadelphia of a small abnormal marker chromosome in patients with chronic myeloid leukemia—the first consistent chromosome abnormality detected in a human malignancy, later designated the Philadelphia chromosome. [3]

  7. Position effect - Wikipedia

    en.wikipedia.org/wiki/Position_effect

    Position effect is the effect on the expression of a gene when its location in a chromosome is changed, often by translocation. This has been well described in Drosophila with respect to eye color and is known as position effect variegation (PEV). [1] The phenotype is well characterised by unstable expression of a gene that results in the red ...

  8. Position-effect variegation - Wikipedia

    en.wikipedia.org/wiki/Position-effect_variegation

    The classical example is the Drosophila w m4 (speak white-mottled-4) translocation. In this mutation , an inversion on the X chromosome placed the white gene next to pericentric heterochromatin, or a sequence of repeats that becomes heterochromatic. [ 3 ]

  9. Site-specific recombination - Wikipedia

    en.wikipedia.org/wiki/Site-specific_recombination

    The mechanism occurs in the framework of a synaptic complex (1) including both DNA sites in parallel orientation. While branch-migration explains the specific homology requirements and the reversibility of the process in a straightforward manner, it cannot be reconciled with the motions recombinase subunits have to undergo in three dimensions.