Convergence - quantifying Parallel & Back Mutations (Part 1)

In a recent post I explored the concept of Convergence and made the point that the mechanism by which Convergence arises is via a combination of Parallel Mutations and Back Mutations in the STR marker values. These mutations are changes that occurred at some time in the past but because they remain hidden to us in the present, we cannot tell when they occurred or how frequently they occurred just by looking at two sets of STR results from people living today.

However, there is a way around this problem. Or at least a partial solution.

By using a combination of STR data and SNP data we have been able to build a Mutation History Tree for the North Tipperary Gleeson's (Lineage II of the Gleason DNA Project). This tree is a "best fit" tree, by which I mean a tree constructed in such a way as to explain the STR & SNP data in the most parsimonious way i.e. with the fewest number of branches that will accommodate or "fit" the data. This approach is also called the "maximum parsimony" approach and is often used when building cladograms or phylogenetic trees. The Mutation History Tree (MHT) is simply another type of cladogram.

But a key point here is that this "best fit" tree is likely to change as more data becomes available. And to illustrate this point, I'm going to compare the current version of the tree (Dec 2016) with the next version that is being prepared following the recent availability of new data from 12 sets of Z255 SNP Pack results.

Below is the current version of the MHT for Lineage II. By comparing each mutation in the tree with every other one, we can identify which mutations are Back Mutations (occurring on a single line of descent) and which are Parallel Mutations (occurring on two or more lines of descent). I have highlighted the Back Mutations in yellow and the Parallel Mutations in green.

Back Mutations in yellow, Parallel Mutations in green
from Gleeson Lineage II MHT (version Dec 2016)

Parallel Mutations occur in the following lines of descent:

• CDYb 40-39 ... A, E, D, F (4 times)
• CDYa 39-38 ... A, B, C, F (4 times)
• 464c 17-16 ... A x2, D (3 times)
• 461 12-11 ... A, B (2 times)
• 576 18-19 ... A, D (2 times)
• 390 23-24 ... A, B, C (3 times)
• 390 24-23 ... B, C (2 times)
• 456 16-15 ... B, D (2 times)
• and so on ...

Back Mutations are more difficult to count, and to conceptualise. Whether you consider the value as mutating forward or back is entirely dependant on your reference point. If our anchor is the upstream Z255 branch, then the original value of marker 390 (for example) is 24, mutating (forward) to 23 on the Z16438 branch, and then back to 24 (in parallel) on Branches A, B & C, and then back to 23 (again in parallel) on Branches B & C. So there are several points to make here:

• this is in fact a Back Mutation that occurs in parallel in 3 separate lines of descent. It is thus both a Back Mutation (relative to its earlier value of 24 on the Z255 branch) and a Parallel Mutation, occurring at (presumably) different time points in Branches A, B & C. It is thus coloured yellow and green.
• It can also be considered a Triple Mutation relative to the Z255 branch - in the sense that it mutates forward to 23 then back to 24, then back to 23 again. But what happens if it flips forward and back 5 times? What would we call that? And what do we call it if it goes two steps forward and one step back? This is where terminology fails us. I'm not sure if there is a standardised way of describing these different kinds of mutation (if there is, please leave a comment below).
• the mutation 390 24-23 occurs in Branches B & C ... relative to its value of 24 in the Z255 branch, this could be considered a Parallel Forward Back Forward Mutation ... for Pete's Sake!!

But if we just focus on the Back Mutations that occur downstream of the branch characterised by the STR mutation (710 36-37), just above the A5627 SNP Block. This "710 branch" incorporates all the Gleeson's of Lineage II, from Branch A to F.* On this overarching branch for Lineage II, the value of the STR marker 390 is 23 and Back Mutations are as follows:

• 390 24-23 ... B, C ... this is the only Back Mutation below the "710 branch"
• And it is also a Parallel Mutation
• All the other yellow Back Mutations are relative to the upstream Z255 branch, and not our downstream "710 branch", and so are not counted in this particular exercise.

So, let's generate some statistics from these numbers:

• The total number of mutations below the "710 branch" (irrespective of whether they are forward or back) is 71.
• There are 69 Forward Mutations (i.e. away from the original value of the relevant marker on the "710 branch")
• There are 2 Back Mutations 
• There are 26 Parallel Mutations
• Forward Mutations outnumber Back Mutations by a ratio of 35.5 : 1
• Parallel Mutations outnumber Back Mutations by a ratio of 13 : 1
• There are 16 people in this tree, and if we make the big assumption that the "710 branch" starts 1000 years ago (i.e. roughly at the time of the introduction of the Gleeson surname), then over the course of 1000 years, the rate of each type of mutation is (crudely) as follows:
• Forward Mutations = 69/16 = 4.3125 mutations per "line of descent" per 1000 years
• Back Mutations = 2/16 = 0.125 mutations per "line of descent" per 1000 years
• Parallel Mutations = 26/16 = 1.625 mutations per "line of descent" per 1000 years

These are crude estimates but they give some idea of the relative importance of Parallel Mutations compared to Back Mutations. And applying this information to the phenomenon of Convergence, it would seem that Back Mutations play a very minor role compared to Parallel Mutations.

In a subsequent post we will see how these calculations stand up when we add in additional data from 12 SNP Pack results and reconfigure the tree into the next version of the "best fit" model. And we will also attempt to quantify the total number of Back & Parallel Mutations below the upstream marker Z255.

Maurice Gleeson

May 2017

* the Big Y results of a 10th member of the group indicate that this branch is characterised by the SNP A5631 although this result is not reflected in this version of the MHT