A
germline mutation is any detectable and heritable variation in the lineage of
germ cells.
Mutations in these cells are transmitted to
offspring, while, on the other hand, those in
somatic cells are not. A germline mutation gives rise to a
constitutional mutation in the offspring, that is, a mutation that is present in virtually every cell. A constitutional mutation can also occur very soon after
fertilisation, or continue from a previous constitutional mutation in a parent.
This distinction is most important in
animals, where germ cells are distinct from somatic cells. However, in
plants, the reproductive cells in a particular flower will be derived from the same
meristem as the cells in that
flower and on the
stem leading to the flower, which is a different population of cells than those that give rise to the other flowers on the plant.
Single-celled organisms have no distinction between germline and somatic tissues.
In animals, mutations are more likely to occur in
sperm than in
ova, because a larger number of cell divisions are involved in the production of sperm.
Mutations that are not
germline are
somatic mutations, which are also called
acquired mutations.
See also
References
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