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Sex linked describes the sex-specific reading patterns of inheritance and presentation when a gene mutation is present on a sex chromosome (allosome) rather than a non-sex chromosome . In humans, these are termed X-linked recessive , X-linked dominant and Y-linked .
X-linked recessive inheritance. X-linked recessive inheritance is a mode of inheritance in which a mutation in a gene on the X chromosome causes the phenotype to be always expressed in males (who are necessarily hemizygous for the gene mutation because they have one X and one Y chromosome) and in females who are homozygous for the gene mutation, see zygosity.
Genetic linkage is the tendency of DNA sequences that are close together on a chromosome to be inherited together during the meiosis phase of sexual reproduction.Two genetic markers that are physically near to each other are unlikely to be separated onto different chromatids during chromosomal crossover, and are therefore said to be more linked than markers that are far apart.
The pattern of inheritance in which a single recessive allele is inherited but is still expressed is known as pseudodominance. This mainly occurs with sex-linked genes (i.e., those on the sex chromosomes). The homogametic sex (females in humans) receive two of each sex chromosome and therefore need to be homozygous to show a recessive trait.
Y-linked inheritance Pedigree tree showing the inheritance of a Y-linked trait. Y linkage, also known as holandric inheritance (from Ancient Greek ὅλος hólos, "whole" + ἀνδρός andrós, "male"), [1] describes traits that are produced by genes located on the Y chromosome. It is a form of sex linkage. Y linkage can be difficult to detect.
Offspring of the males with the trait don't inherit the trait. Offspring of the females with the trait always inherit the trait (independently from their own sex). Extranuclear inheritance (also known as cytoplasmic inheritance) is a form of non-Mendelian inheritance also first discovered by Carl Correns in 1908. [9]
Mutations inherited through the chromosomes can be autosomal dominant or recessive and can also be sex-linked dominant or recessive. Chromosomal inheritance follows normal Mendelian laws, despite the fact that the phenotype of the disease may be masked.
Sex linkage was first reported by Doncaster and Raynor in 1906 [2] who studied the inheritance of a colour mutation in a moth, Abraxas grossulariata. Thomas Hunt Morgan later showed that a new white-eye mutation in Drosophila melanogaster was also sex-linked. He found that a white-eyed male crossed with a red-eyed female produced only red-eyed ...