- Open Access
© Gabriel et al; licensee BioMed Central Ltd. 2010
- Received: 20 October 2010
- Accepted: 21 October 2010
- Published: 26 October 2010
Several recent papers, including one in BMC Evolutionary Biology, examine the colonization history of house mice. As well as background for the analysis of mouse adaptation, such studies offer a perspective on the history of movements of the humans that accidentally transported the mice.
See research article: http://www.biomedcentral.com/1471-2148/10/325
- House Mouse
- Colonization History
- Northeastern Atlantic Ocean
- Western Subspecies
- Overland Route
Hardouin et al.'s study  involved 437 mice from Kerguelen, an unprecedented coverage for the analysis of colonization history of such a small area. They found remarkable consistency in the mitochondrial DNA (mtDNA) sequences on Grande Terre and most of the surrounding small islands, suggesting that these populations are the product of a single relatively recent colonization (ultimately deriving from Europe). This fits with the recorded discovery of the archipelago in 1772 (by a Frenchman called Kerguelen-Trémarec) and settlement by mice either at the time or with subsequent human arrivals. Two of the other small islands in the archipelago (Cochons and Cimetière) may have been colonized in a second, separate introduction, as their mice belong to a different mtDNA lineage (also ultimately European). Over the archipelago as a whole there was no evidence of within-island heterogeneity in terms of mtDNA lineage. This is surprising given the large number of ships carrying mice that would have visited the islands (coming from many different places and therefore carrying mice of many different mtDNA lineages). These results are consistent with other data  suggesting that mouse populations are resistant to secondary invasion by females (mtDNA is a maternally inherited marker). Presumably, newly arriving females coming into an established population are generally unable to survive or gain mates, and in consequence do not contribute to the population's gene pool. All of this means that mtDNA may be a very good marker for initial colonization by house mice within a given area.
Studies by ourselves and others have looked at the mtDNA lineages of house mice in northern Europe. A different lineage from those typically seen in Mediterranean Europe has been found further north in the area between Britain and Germany [2, 5]. The mouse mtDNA again matches a regional sphere of influence of Iron Age people , and, unlike other mouse mtDNA lineages, it appears that this Anglo-German lineage did not arrive in northern Europe by an overland route; instead it probably came along the Atlantic coast (Figure 1).
mtDNA studies suggest another pulse of detectable mouse colonizations during Viking times (Figure 1). Like the Phoenicians, the Vikings were impressive seafarers, carrying substantial cargoes ideal for stowaway mice, and there are mtDNA signals of maritime colonization events [2, 5, 7, 8].
How did Mus musculus domesticus get from Europe to Kerguelen? This subspecies had been in the right place at the right time to make use of the first storage of grain by Neolithic humans in the Fertile Crescent in the Middle East, and to adapt to changing human cultural practices. Good fortune struck again when the subspecies found itself in western Europe at the time that British, Dutch, French and Iberian seafarers were 'discovering', exploiting and taking settlers to the rest of the world. Kerguelen-Trémarec and his crew may have been the first humans to see the archipelago that now bears his name, but the colonization route of the first mice to arrive there is still uncertain, although their starting point was certainly western Europe (Figure 1).
It is intriguing how far the linkage between human history and mouse history may go. Jones et al.  found a correlation between mouse genetic diversity and human population size (proportional to amount of mouse habitat) in discrete areas of the Faroe Islands in the northeastern Atlantic Ocean, another archipelago where house mice have been studied. This supports the expectation that the population genetics (in terms of genetic response to population expansions and contractions) of house mice is likely to reflect rather closely the population genetics of humans.
We have been considering how the history of humans impacts on the genetics of the house mouse, but that can be turned around. If the history of house mice is so intimately determined by humans, then the genetics of house mice may be useful to answer human historical questions; for example, the details of human affiliations in the Iron Age are sometimes imprecise - might house mice be able to indicate associations between Iron Age people from different geographical areas? House mice are equivalent to an artifact that an archeologist discovers and uses to determine human colonization or trading routes. The provenance of the mice is established from their DNA sequence and that is a very powerful tool, given its extraordinary information content. Not only can the DNA sequence help to establish the source of the mice found in a particular place but it can be used to date the original colonization and subsequent population history (including secondary colonizations), following approaches used for human DNA (see, for example )). However, it is clear from all the recent papers considered here [1, 3, 5, 7, 8] that archeogenetics using house mice is at an early stage, and that, in particular, calibrations to generate an accurate mouse mtDNA molecular clock are urgently needed. Hardouin et al.  comment that, for the mtDNA region analyzed, they found a much higher mutation rate than suggested by previous studies. Further work should follow up this finding and also use other subspecies to globalize the opportunities for applying mice as a proxy to study humans, following the lead of another recent paper .
SIG was funded by the scholarship SFRH/BD/21437/2005 from Fundação para a Ciência e a Tecnologia (Portugal), FJ and JBS by Cornell University (USA) and EPJ by the Carl Trygger Foundation (Sweden). We are grateful to Angela Douglas for her comments on the manuscript.
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