Why should you consider testing your older relatives before exploring your own genetic genealogy?
The answer lies in genetic inheritance patterns. There are four types of genetic inheritance patterns which genetic genealogists apply to family history research: mtDNA, Y-DNA, X-DNA, and autosomal DNA.
Mitochondrial DNA (mtDNA) is inherited from an individual’s mother. She, in turn, inherited it from her mother in a line of direct maternal inheritance. Your mitochondrial DNA will be similar, if not the same, as the mitochondrial DNA of your siblings, your maternal aunts and uncles, and many other maternal relatives. The Y-chromosome (Y-DNA) or the male sex chromosome is inherited by males from their father, who in turn inherited it from his father in a direct line of paternal inheritance. A male’s Y chromosome will be similar, if not identical, to the Y-DNA of his full brothers, paternal uncles, and other paternal relatives.
Because of the direct inheritance patterns of mitochondrial and Y-DNA, it is possible to determine the Y-DNA and mitochondrial DNA signatures of deceased ancestors by selectively testing known individuals. In this regard, it may not be as urgent that you test your older relatives for their Y-DNA and mtDNA unless they are the last living representatives who carry that DNA. For example, if your father had only daughters and he had no siblings, then it would be important to test his Y-DNA since he may be the last living close relative with that information. You may also want to test his mtDNA for the same reason. Even when there are other relatives who could stand in and represent the DNA of an older relative, occasionally mutations are introduced in Y-DNA and mtDNA lineages, so it is still a good idea to test older relatives.
While there may be situations in which you would prioritize testing older relatives for Y-DNA and mtDNA testing, it is more common to prioritize testing the autosomal DNA of elderly relatives.
An autosomal DNA test, such as the MyHeritage DNA test, will include information regarding X-DNA and autosomal DNA. The X chromosome is the female sex chromosome. Males inherit one X chromosome from their mother, whereas females inherit one from their mother and one from their father. Rather than inheriting a second X chromosome, males inherit a Y chromosome from their father. The remaining 22 pairs of chromosomes in human cells are known as the autosomal DNA. Each individual inherits 50% of their autosomal DNA from their mother and 50% from their father. Beyond that, they inherit approximately 25% from each grandparent and approximately half the previous amount from every subsequent generation of ancestry. Eventually, due to the random nature of autosomal DNA inheritance, there will be some ancestors from whom an individual does not inherit significant portions of their autosomal DNA.
Any autosomal or X-DNA you inherit from a specific ancestor has to be less than or equal to the amount of DNA that your parent inherited from that same ancestor which in turn is a subset of the DNA that your grandparent inherited from that same ancestor. While your grandmother may share 25% of her DNA with your great-great-grandparent, you will share only about 6% of your DNA with that same ancestor. The more DNA a test subject shares with an ancestor, the more matches they will have who are related through that same ancestor. The more matches they have who are related through an ancestor of interest, the higher the chance is that they will be able to make genealogical discoveries through collaboration, correspondence, and analysis. For these reasons, priority for your autosomal DNA testing should be given to older relatives who share more DNA in common with your ancestors than you do.
Another way to view this prioritization is through the concept of coverage. By testing yourself, 100% of your autosomal DNA will be represented in a database, 50% of your parents’ DNA will be represented, and 25% of each of your grandparents’ DNA will be represented. Though each individual inherits 50% of their DNA from each parent, siblings inherit different 50% portions. Though they will share some DNA in common with a sibling, they will also carry unique DNA. By testing a sibling, you could obtain approximately 75% coverage of your parents’ DNA and about 37% coverage of each of your grandparents’ DNA. To achieve 95% coverage of a deceased parent, on average, it is necessary to test four of their living children. If they had fewer than four children or if they do not have other living descendants, there are severe limitations on how much of their DNA can be recovered and represented in the database through testing of their descendants.
By testing your older relatives, you ensure that their DNA will be represented in the current databases and you increase the chance that future generations will be able to connect with them through these means.
If you’ve tested at another company, now is an ideal time to cast a wider net for possible genetic matches by uploading your raw data to MyHeritage. You’ll receive DNA Matches for free, which will help you discover more new relatives based on shared DNA.
Though we as genealogists have begun to treat DNA as we would other records in our analysis, correlation, and proof arguments, we also need to start thinking like archivists and dedicate time and effort to acquiring and preserving DNA records so that the information of our ancestors’ DNA will be available for future generations of researchers. Don’t wait until it’s too late. Test your older relatives today!
