Blood type inheritance is a fundamental concept in human genetics that follows Mendelian inheritance patterns. The ABO blood group system, discovered by Karl Landsteiner in 1901, is controlled by three alleles: A, B, and O. These alleles determine the presence of specific antigens on red blood cells and corresponding antibodies in plasma. Understanding blood type inheritance is crucial for medical applications, including blood transfusions, organ transplants, and genetic counseling.
The ABO Blood Group System
The ABO system consists of four main blood types: A, B, AB, and O. Blood type A individuals have A antigens on their red blood cells and anti-B antibodies in their plasma. Blood type B individuals have B antigens and anti-A antibodies. Blood type AB individuals have both A and B antigens but no antibodies, making them universal recipients. Blood type O individuals have no A or B antigens but both anti-A and anti-B antibodies, making them universal donors.
Rh Factor and Its Genetic Basis
The Rh factor, discovered in 1940, is another important blood group system. Rh-positive (Rh+) individuals have the D antigen on their red blood cells, while Rh-negative (Rh-) individuals lack this antigen. The Rh factor is inherited independently of the ABO system, following simple dominant-recessive inheritance where Rh+ is dominant and Rh- is recessive. This creates eight possible blood types: A+, A-, B+, B-, AB+, AB-, O+, and O-.
Genetic Alleles and Inheritance Patterns
Blood type inheritance follows specific genetic rules. The A and B alleles are codominant, meaning both can be expressed simultaneously in AB individuals. The O allele is recessive to both A and B. Each person inherits one allele from each parent, resulting in six possible genotypes: AA, AO, BB, BO, AB, and OO. The Rh factor follows simple dominant-recessive inheritance, where Rh+ (D) is dominant over Rh- (d).