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  2. Exonuclease 1 - Wikipedia

    en.wikipedia.org/wiki/Exonuclease_1

    Exonuclease 1 is an enzyme that in humans is encoded by the EXO1 gene. [ 5 ] [ 6 ] [ 7 ] This gene encodes a protein with 5' to 3' exonuclease activity as well as RNase activity (endonuclease activity cleaving RNA on DNA/RNA hybrid). [ 8 ]

  3. Meiotic recombination checkpoint - Wikipedia

    en.wikipedia.org/wiki/Meiotic_recombination...

    Meiotic sex chromosome inactivation only happens in male, which may partially be the reason why only Spo11 mutant spermatocytes but not oocytes fail to transition from prophase I to metaphase I. [3] [8] However the asynapsis does not happen only within sex chromosomes, and such transcription regulation was suspended until it was further ...

  4. Chromosomal crossover - Wikipedia

    en.wikipedia.org/wiki/Chromosomal_crossover

    Crossing over occurs between prophase I and metaphase I and is the process where two homologous non-sister chromatids pair up with each other and exchange different segments of genetic material to form two recombinant chromosome sister chromatids. It can also happen during mitotic division, [1] which may

  5. Genetic recombination - Wikipedia

    en.wikipedia.org/wiki/Genetic_recombination

    Most recombination occurs naturally and can be classified into two types: (1) interchromosomal recombination, occurring through independent assortment of alleles whose loci are on different but homologous chromosomes (random orientation of pairs of homologous chromosomes in meiosis I); & (2) intrachromosomal recombination, occurring through ...

  6. X chromosome - Wikipedia

    en.wikipedia.org/wiki/X_chromosome

    Klinefelter syndrome can also result from an extra X chromosome in only some of the body's cells. These cases are called mosaic 46,XY/47,XXY. Trisomy X. This syndrome results from an extra copy of the X chromosome in each of a female's cells. Females with trisomy X have three X chromosomes, for a total of 47 chromosomes per cell.

  7. Homologous recombination - Wikipedia

    en.wikipedia.org/wiki/Homologous_recombination

    During meiosis, homologous recombination can produce new combinations of genes as shown here between similar but not identical copies of human chromosome 1. Homologous recombination is a type of genetic recombination in which genetic information is exchanged between two similar or identical molecules of double-stranded or single-stranded ...

  8. Helicase - Wikipedia

    en.wikipedia.org/wiki/Helicase

    One label is a fluorescent lanthanide chelate, which serves as the label that is monitored through an adequate 96/384 well plate reader. The other label is an organic quencher molecule. The basis of this assay is the "quenching" or repressing of the lanthanide chelate signal by the organic quencher molecule when the two are in close proximity ...

  9. Bloom syndrome protein - Wikipedia

    en.wikipedia.org/wiki/Bloom_syndrome_protein

    Recombination during meiosis is often initiated by a DNA double-strand break (DSB). During recombination, sections of DNA at the 5' ends of the break are cut away in a process called resection. In the strand invasion step that follows, an overhanging 3' end of the broken DNA molecule then "invades" the DNA of an homologous chromosome that is ...