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Life Science Dictionary

Mendelian inheritance

Genetics · Medicine

Say it: men-DEE-lee-un in-HEH-rih-tuns

Mendelian inheritance is the pattern by which single genes pass from parents to offspring, following the laws of segregation and independent assortment.

Also: Mendelism, Mendel's laws

Definition

What is mendelian inheritance?

Mendelian inheritance describes how traits controlled by single genes are passed from one generation to the next, following rules first worked out by Gregor Mendel, a monk in Brno. From crosses of thousands of pea plants, published in 1866, Mendel showed that traits do not blend but are carried by separate units, now called genes, that come in pairs. His work was largely ignored until it was rediscovered in 1900.

Three principles sum up the pattern. Under dominance, one allele can hide the effect of another in a heterozygote. Under the law of segregation, the two alleles of a gene separate when gametes form, so each gamete gets just one. Under the law of independent assortment, alleles of different genes sort into gametes independently of each other. Both laws follow from how chromosomes behave in meiosis, and together they explain the 3:1 and 9:3:3:1 ratios that Punnett squares predict.

In human genetics, Mendelian conditions are those caused mainly by a single gene; they follow autosomal dominant, autosomal recessive or X-linked patterns in pedigrees. Linked genes, incomplete dominance and traits shaped by many genes all depart from Mendel's simple ratios.

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