![]() |
| Figure 1: Genetic Inheritance of X Chromosome Sex Linked Conditions (Source: Boundless, 2019) |
Today’s blog post is dedicated to expanding on previously discussed Mendelian genetic content, specifically addressing sex-linked genetic inheritance. Prior to reading this post it is important that you have the appropriate background to understand this post’s content. You will need an understanding of Mendelian genetics, dominant and recessive alleles, as well as how genetic inheritance is understood through Punnett Squares. If you do not already understand these terms or have the required background please click on the hyperlinks provided in the previous sentence so you can read and catch up on these topics.
Sex linked traits are genes present on a sex chromosome (typically the X or Y chromosome). These chromosomes are often referred to as the sex chromosomes because they determine the sex of individuals. Males carry one X and one Y chromosome, whereas females carry two X chromosomes. These chromosomes not only determine biological sex of the individual, but they also genetically affect the individual in other ways since both chromosomes carry genetic information. The X chromosome, which is larger, carries approximately 1098 genes, while the smaller Y chromosome carries 26 genes, which largely relate to sperm production and other nominal activities.
There are a variety of X linked genetic conditions out there. These include but are not limited to hemophilia, red-green color blindness, congenital night blindness, some high blood pressure genes, Duchenne muscular dystrophy, and also Fragile X syndrome. Women can either display/present with these conditions or they can be carriers, the latter of which results in them having (or carrying) one recessive allele (or copy) of the gene, but men will always express the X chromosome genetic condition since they only carry one X chromosome.
Males receive their X chromosome from their mothers (a result of the fact that be born a male their father’s must provide the Y chromosome), which in turn explains why X chromosome conditions in males are often blamed on the mother. Since males only carry one X chromosome they are forced to express whichever allele of the gene (be it dominant or recessive) is present on the X chromosome. This means that males have a 50/50 chance of expressing either a dominant or recessive allele for X chromosome conditions, while women do not (Figure 1). Due to the presence of a Y chromosome in males they are the only individuals who can carry and pass on Y linked genes. Y chromosome conditions can only be present in females if and when they carry the Y chromosome, which is typically a third copy of a chromosome.
References
Boundless. (2019, November 19). 12.2E: Sex-Linked Traits . Retrieved from Biology: Libre Texts: https://bio.libretexts.org/Bookshelves/Introductory_and_General_Biology/Book%3A_General_Biology_(Boundless)/12%3A_Mendel%27s_Experiments_and_Heredity/12.2%3A__Patterns_of_Inheritance/12.2E%3A_Sex-Linked_Traits
Easter, C. (No Date). Sex Linked. Retrieved from National Human Genome Research Institute: https://www.genome.gov/genetics-glossary/Sex-Linked
O'Neil, D. (2012). Sex Linked Genes. Retrieved from Palomar Anthropology Biology Basics: https://www2.palomar.edu/anthro/biobasis/bio_4.htm


