Genetic variability

<h2 id="causes">Causes</h2>
There are many sources of genetic variability in a population:

<ul><li><a href="/facts/Homologous_recombination/WU0IIVVv">Homologous recombination</a> is a significant source of variability. During <a href="/facts/Meiosis/Pj5Q6nGN">meiosis</a> in sexual organisms (<a href="/facts/Sexual_reproduction/hmsXy53s">sexual reproduction</a>), two <a href="/facts/Homologous_chromosomes/hktsBhyx">homologous chromosomes</a> cross over one another and exchange genetic material. This random process of exchanging genetic material is known as recombination, and it is governed by its own set of genes.<a class="footnote-ref" id="fnref:3" href="#fn:3">3</a> Being controlled by genes means that recombination is variable in frequency. Generally, it is more common in areas on the chromosome where there are a higher number of genes. It creates more combinations of genes.<a class="footnote-ref" id="fnref:4" href="#fn:4">4</a> After this occurs, the chromosomes are split apart and are ready to contribute to forming an offspring.</li>
<li><a href="/facts/Immigration/8vNxfBhT">Immigration</a>, <a href="/facts/Emigration/TINd6wC0">emigration</a>, and <a href="/facts/Species_translocation/jYyVod10">translocation</a> – each of these is the movement of an individual into or out of a population. When an individual enters a new population after coming from a genetically isolated one, they will increase the genetic variability of the next generation, provided that they reproduce.<a class="footnote-ref" id="fnref:5" href="#fn:5">5</a></li>
<li><a href="/facts/Polyploidy/L7xyKHdK">Polyploidy</a> – having more than two homologous chromosomes. This allows for more recombination during meiosis and more genetic variability in one's offspring. However, this phenomenon can also prove difficult for <a href="/facts/Cell_division/n5MrunWj">cell division</a>.<a class="footnote-ref" id="fnref:6" href="#fn:6">6</a></li>
<li>Diffuse centromeres – in <a href="/facts/Asexual_reproduction/HpovW0VS">asexual</a> organisms where the offspring is an exact genetic copy of the parent, there are limited sources of genetic variability. One thing that increases variability, however, is having diffused centromeres instead of localized <a href="/facts/Centromeres/AWxF1ClY">centromeres</a>. Being diffused allows the <a href="/facts/Chromatids/fQ68yxMn">chromatids</a> to split apart in many different ways, which produces chromosome fragmentation and polyploidy.<a class="footnote-ref" id="fnref:7" href="#fn:7">7</a></li>
<li>Genetic <a href="/facts/Mutations/Ee4NnWbY">mutations</a> – contribute to the genetic variability within a population and can have positive, negative, or neutral effects on a fitness.<a class="footnote-ref" id="fnref:8" href="#fn:8">8</a> This variability can be easily propagated throughout a population by <a href="/facts/Natural_selection/JXTte6en">natural selection</a> if the mutation increases the affected individual's <a href="/facts/Fitness_(biology)/MYpAGGey">fitness</a> and its effects will be minimized/hidden if the mutation is deleterious. If the individual can survive with the mutations they have, those mutations will likely be passed down to offspring. However, the smaller a population and its genetic variability are, the more likely the recessive/hidden deleterious mutations will show up causing <a href="/facts/Genetic_drift/lvoEEctX">genetic drift</a>.<a class="footnote-ref" id="fnref:9" href="#fn:9">9</a></li></ul>
DNA damages are very frequent, occurring more than 60,000 times a day per cell on average in humans. This is due to <a href="/facts/Metabolism/WxDrm8k5">metabolic</a> or <a href="/facts/Hydrolysis/JTvwIHPs">hydrolytic</a> processes as summarized in <a href="/facts/DNA_damage_(naturally_occurring)/CjGTLKGl">DNA damage (naturally occurring)</a>. Most DNA damages are accurately repaired by various natural <a href="/facts/DNA_repair/hsURuYYq">DNA repair</a> mechanisms. However, some DNA damages remain and give rise to mutations.
Additionally, not all types of mutations occur as much as others do. Some mutations might have a huge impact on the human body, and some might not. It depends on what combination of base pairs is changed.<a class="footnote-ref" id="fnref:10" href="#fn:10">10</a>
Most spontaneously arising mutations result from error prone replication (translesion synthesis) past a DNA damage in the template strand. For example, in yeast more than 60% of spontaneous single-base pair substitutions and deletions are likely caused by <a href="/facts/DNA_repair/hsURuYYq">translesion synthesis</a>.<a class="footnote-ref" id="fnref:11" href="#fn:11">11</a> Another significant source of mutation is an inaccurate DNA repair process, non-homologous end joining, that is often employed in repair of DNA double-strand breaks.<a class="footnote-ref" id="fnref:12" href="#fn:12">12</a> (Also see <a href="/facts/Mutation/Ee4NnWbY">Mutation</a>.) Thus, it seems that DNA damages are the underlying cause of most spontaneous mutations, either because of error-prone replication past damages or error-prone repair of damages.
<h2 id="factors-that-decrease-genetic-variability">Factors that decrease genetic variability</h2>
There are many sources that decrease genetic variability in a population:

<ul><li>Habitat loss, including:
<ul><li><a href="/facts/Habitat_fragmentation/uVIVdT70">Habitat fragmentation</a> produces discontinuity in an organism's habitat, so that interbreeding is limited. Fragmentation can be caused by many factors, including geological processes or a human-caused events. Fragmentation may further allow <a href="/facts/Genetic_drift/lvoEEctX">genetic drift</a> to lower local <a href="/facts/Genetic_diversity/GIymbUr8">genetic diversity</a>.</li>
<li><a href="/facts/Climate_change_(general_concept)/D3X6Ulbu">Climate change</a> is a drastic and enduring change in weather patterns. By driving species out of their <a href="/facts/Fundamental_niche/YnhNkL2e">fundamental niche</a>, climate change can lower population size and consequently lower genetic variation.</li></ul></li>
<li>The <a href="/facts/Founder_effect/5hRhkbSF">founder effect</a>, which occurs when a population is founded by few individuals.</li></ul>
<h2 id="see-also">See also</h2>
<ul><li><a href="/facts/Evolvability/xI5fGCTV">Evolvability</a></li>
<li><a href="/facts/Human_genetic_variation/bgU0WXSf">Human genetic variation</a>
<ul><li><a href="/facts/Personalized_medicine/rawUyWgd">Personalized medicine</a></li></ul></li>
<li><a href="/facts/Microevolution/Xwkz6zCf">Microevolution</a></li>
<li><a href="/facts/Mutation/Ee4NnWbY">Mutation</a></li>
<li><a href="/facts/Genetic_drift/lvoEEctX">Genetic drift</a></li>
<li><a href="/facts/Gene_flow/EuvXPhHt">Gene flow</a></li>
<li><a href="/facts/Glossary_of_genetics_and_evolutionary_biology/MXNShPhw">Glossary of genetics and evolutionary biology</a></li></ul>

<h2 id="references">References</h2>

<ol>
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<li id="fn:2">Sousa, P., Froufe, E., Harris, D.J., Alves, P.C. & Meijden, A., van der. 2011. Genetic diversity of Maghrebian Hottentotta (Scorpiones: Buthidae) scorpions based on CO1: new insights on the genus phylogeny and distribution. African Invertebrates 52 (1)."Archived copy". Archived from the original on 2011-10-04. Retrieved 2011-05-03.{{cite web}}: CS1 maint: archived copy as title (link) <a href="/wiki/African_Invertebrates" target="_blank">/wiki/African_Invertebrates</a> <a href="#fnref:2" class="footnote-back-ref">↩</a></li>
<li id="fn:3">Stapley J, Feulner PG, Johnston SE, Santure AW, Smadja CM (2017-12-19). "Recombination: the good, the bad and the variable". Philosophical Transactions of the Royal Society B: Biological Sciences. 372 (1736): 20170279. doi:10.1098/rstb.2017.0279. ISSN 0962-8436. PMC 5698631. PMID 29109232. <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698631" target="_blank">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698631</a> <a href="#fnref:3" class="footnote-back-ref">↩</a></li>
<li id="fn:4">Stapley J, Feulner PG, Johnston SE, Santure AW, Smadja CM (2017-12-19). "Recombination: the good, the bad and the variable". Philosophical Transactions of the Royal Society B: Biological Sciences. 372 (1736): 20170279. doi:10.1098/rstb.2017.0279. ISSN 0962-8436. PMC 5698631. PMID 29109232. <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698631" target="_blank">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698631</a> <a href="#fnref:4" class="footnote-back-ref">↩</a></li>
<li id="fn:5">Ehrich, Dorothy, Per Erik Jorde (2005). "High Genetic Variability Despite High-Amplitude Population Cycles in Lemmings". Journal of Mammalogy. 86 (2): 380–385. doi:10.1644/BER-126.1. <a href="https://doi.org/10.1644%2FBER-126.1" target="_blank">https://doi.org/10.1644%2FBER-126.1</a> <a href="#fnref:5" class="footnote-back-ref">↩</a></li>
<li id="fn:6">Zhang S, Lin YH, Tarlow B, Zhu H (2019-06-18). "The origins and functions of hepatic polyploidy". Cell Cycle. 18 (12): 1302–1315. doi:10.1080/15384101.2019.1618123. ISSN 1538-4101. PMC 6592246. PMID 31096847. <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6592246" target="_blank">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6592246</a> <a href="#fnref:6" class="footnote-back-ref">↩</a></li>
<li id="fn:7">Linhart, Yan, Janet Gehring (2003). "Genetic Variability and its Ecological Implications in the Clonal Plant Carex scopulurum Holm. In Colorado Tundra". Arctic, Antarctic, and Alpine Research. 35 (4): 429–433. doi:10.1657/1523-0430(2003)035[0429:GVAIEI]2.0.CO;2. ISSN 1523-0430. S2CID 86464133. <a href="/wiki/Doi_(identifier)" target="_blank">/wiki/Doi_(identifier)</a> <a href="#fnref:7" class="footnote-back-ref">↩</a></li>
<li id="fn:8">Wills, Christopher (1980). Genetic Variability. New York: Oxford University Press. ISBN 978-0-19-857570-2. <a href="978-0-19-857570-2" target="_blank">978-0-19-857570-2</a> <a href="#fnref:8" class="footnote-back-ref">↩</a></li>
<li id="fn:9">Wills, Christopher (1980). Genetic Variability. New York: Oxford University Press. ISBN 978-0-19-857570-2. <a href="978-0-19-857570-2" target="_blank">978-0-19-857570-2</a> <a href="#fnref:9" class="footnote-back-ref">↩</a></li>
<li id="fn:10">Eichler EE (2019-07-04). "Genetic Variation, Comparative Genomics, and the Diagnosis of Disease". New England Journal of Medicine. 381 (1): 64–74. doi:10.1056/NEJMra1809315. ISSN 0028-4793. PMC 6681822. PMID 31269367. <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6681822" target="_blank">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6681822</a> <a href="#fnref:10" class="footnote-back-ref">↩</a></li>
<li id="fn:11">Kunz BA, Ramachandran K, Vonarx EJ (April 1998). "DNA sequence analysis of spontaneous mutagenesis in Saccharomyces cerevisiae". Genetics. 148 (4): 1491–505. doi:10.1093/genetics/148.4.1491. PMC 1460101. PMID 9560369. <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1460101" target="_blank">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1460101</a> <a href="#fnref:11" class="footnote-back-ref">↩</a></li>
<li id="fn:12">Huertas P (January 2010). "DNA resection in eukaryotes: deciding how to fix the break". Nat. Struct. Mol. Biol. 17 (1): 11–6. doi:10.1038/nsmb.1710. PMC 2850169. PMID 20051983. <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2850169" target="_blank">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2850169</a> <a href="#fnref:12" class="footnote-back-ref">↩</a></li>
</ol>

Genetic variability open-in-new

Genetic variability