Recombination or cross-overs is what occurs during meiosis when creating the reproductive cells. Instead of creating identical copies of each chromosome strand (or non-sister chromatid), a mixed or merged copy is created. That is, a parent does not simply pass one of their chromosomes as they got it from one of their parents, but a merge of the two chromosomes they have from each parent.
We each have a homologous pair of autosome chromosomes. That is, one copy or strand from our father and one from our mother. If recombining did not occur, that copy passed on to a child would be identical to the one they got from one of their parents. But this would lead to less genetic diversity. So during meiosis, when creating the copy of an autosome, a cut occurs where all of a sudden, instead of copying the paternal chromosome it starts copying the maternal one. And then vice-a-versa as it moves on down making a copy of the chromosome.
This is a key feature that greatly impacts the properties studied in genetic genealogy and is only more recently taught in schools. (That is, older adults may have missed this learning from their high school biology class as it was not generally known yet.)
Recombining causes a few key features:
Studies have shown that only 30 to 50 cross-overs occur across all the autosomes in each reproductive cell. Therefore maybe 2 to 3 cuts in chromosome 1 and maybe none in chromosome 22, on average. Or a cross-over every 100cM. (Get why the invention of the centiMorgan now?) For as yet not understood reasons, genetic genealogists are noticing that there are almost twice as many cross-overs in the chromosomes from a mother than come from a father. Hence the wider variance on cross-over measures.
Due to the statistical variance of these cuts, segments of DNA shorter than about 20cM have a small chance of being broken up by recombination. Hence, once shared segment lengths reach this size or smaller, they tend to stick around intact for a few generations and then simply disappear completely due to the chance of simply not being in the portion of DNA passed down. This it is not uncommon to see 3 tested generations to have a single, same length matching segment in common with a distant cousin. Realize it is more common to not share any segments at all with the more distant cousin than to share that same matching segment. For these small segments, the 50% probability of being passed down is much greater than the probability of being broken up smaller.
As an example, consider your mother's Chromosome 1. If she only passed one or the other copy she had, in its entirety, then the grandchild would only have all of the maternal grandmothers chromosome 1 or all of the maternal grandfathers chromosome 1. So if recombining did not occur, as the above implies, the "discreteness" in passing down the full chromosome or not would lead to a greater variation in DNA sharing between siblings and subsequent generations; thus a greater variance in features and such between them as well. But instead, because of recombination, the mother creates a unique chromosome 1 mixture of her two strands of chromosome 1 in each reproductive cell (i.e. the egg). This leads to a finer grain. more equitable mixing of the DNA passed down to a child from the grandparents.
Note: Even children have cross-overs when compared to their parents. But this is only evident if using phased results and looking at the phased-chromosome comparison. Children of a parent should have more than 22 segments but often, because all their DNA is coming from the parent on each chromosome, each chromosome appears as one long matching segment in pseudo-half-identical tools. Comparing siblings brings out the number of cross-overs each carries.
We each have a homologous pair of autosome chromosomes. That is, one copy or strand from our father and one from our mother. If recombining did not occur, that copy passed on to a child would be identical to the one they got from one of their parents. But this would lead to less genetic diversity. So during meiosis, when creating the copy of an autosome, a cut occurs where all of a sudden, instead of copying the paternal chromosome it starts copying the maternal one. And then vice-a-versa as it moves on down making a copy of the chromosome.
This is a key feature that greatly impacts the properties studied in genetic genealogy and is only more recently taught in schools. (That is, older adults may have missed this learning from their high school biology class as it was not generally known yet.)
Recombining causes a few key features:
- Chromosomes are broken up and mixed when the reproductive cells are created by each parent; thus giving a more even mixture of the DNA from the grandparents
- Full siblings chromosome matching segments are more homogeneous and average tightly around 50% total sharing because of this finer grain mixing that occurs
- ...
Studies have shown that only 30 to 50 cross-overs occur across all the autosomes in each reproductive cell. Therefore maybe 2 to 3 cuts in chromosome 1 and maybe none in chromosome 22, on average. Or a cross-over every 100cM. (Get why the invention of the centiMorgan now?) For as yet not understood reasons, genetic genealogists are noticing that there are almost twice as many cross-overs in the chromosomes from a mother than come from a father. Hence the wider variance on cross-over measures.
Due to the statistical variance of these cuts, segments of DNA shorter than about 20cM have a small chance of being broken up by recombination. Hence, once shared segment lengths reach this size or smaller, they tend to stick around intact for a few generations and then simply disappear completely due to the chance of simply not being in the portion of DNA passed down. This it is not uncommon to see 3 tested generations to have a single, same length matching segment in common with a distant cousin. Realize it is more common to not share any segments at all with the more distant cousin than to share that same matching segment. For these small segments, the 50% probability of being passed down is much greater than the probability of being broken up smaller.
As an example, consider your mother's Chromosome 1. If she only passed one or the other copy she had, in its entirety, then the grandchild would only have all of the maternal grandmothers chromosome 1 or all of the maternal grandfathers chromosome 1. So if recombining did not occur, as the above implies, the "discreteness" in passing down the full chromosome or not would lead to a greater variation in DNA sharing between siblings and subsequent generations; thus a greater variance in features and such between them as well. But instead, because of recombination, the mother creates a unique chromosome 1 mixture of her two strands of chromosome 1 in each reproductive cell (i.e. the egg). This leads to a finer grain. more equitable mixing of the DNA passed down to a child from the grandparents.
Note: Even children have cross-overs when compared to their parents. But this is only evident if using phased results and looking at the phased-chromosome comparison. Children of a parent should have more than 22 segments but often, because all their DNA is coming from the parent on each chromosome, each chromosome appears as one long matching segment in pseudo-half-identical tools. Comparing siblings brings out the number of cross-overs each carries.
External References
- Wikipedia Homologous Recombination
- UCDavis Coop Lab paper on simulation of segment inheritance.