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The Death of |
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By:
Brad Harrub, Ph.D.*It was not forbidden fruit that caused her demise this time. “Mitochondrial Eve,” as many knew her, has been dethroned and awaits her entombment due to new facts that have recently surfaced. For decades now men have been trying to determine the geographical origin of humans: whether we all came from one specific locale, or whether there were many small pockets of people placed all around the world. It appeared that the battle was won in the late 1980s when geneticists unleashed a startling discovery. They found that DNA located in the nucleus of a cell was different from the DNA found outside the nucleus, in organelles called mitochondria. Realizing that the DNA in mitochondria was not a product of procreation, and knowing that eggs destroy sperm following fertilization, scientists speculated that mitochondrial traits, including a variety of inherited disorders, were exclusively passed down from the mother. This discovery brought with it another
revelation. If humans received mitochondrial DNA (mtDNA) from only their
mothers, then researchers could “map” a family tree using that
information. Thus, a hypothesis was formed that included a “molecular
clock” of evolution, which emerged from early observations that DNA
tended to mutate linearly with time. If indeed, mtDNA evolved at
constant rates, then it could serve as a molecular clock for timing
evolutionary events and reconstructing the evolutionary history of
extant species. Given enough information, scientists believed they could
accurately show where humans had originated--thus “mitochondrial Eve.” A recent study noted: Women have struggled to gain equality in society, but biologists have long thought that females wield absolute power in a sphere far from the public eye: in the mitochondria, cellular organelles whose DNA is thought to pass intact from mother to child with no paternal influence. On page 2524 however, a study by Philip Awadalla of the University of Edinburgh and Adam Eyre-Walker and John Maynard Smith of the University of Sussex in Brighton, U.K. finds signs of mixing between maternal and paternal mitochondrial DNA (mtDNA) in humans and chimpanzees. Because biologists have used mtDNA as a
tool to trace human ancestry and relationships, the finding has
implications for everything from the identification of bodies to the
existence of a “mitochondrial Eve” 200,000 years ago (Strauss, 1999, p.
2436). Several recent papers, however, have suggested that elements of mtDNA may sometimes be inherited from the father. This hypothesis is based on evidence that mtDNA may undergo recombination. If this does occur, maternal mtDNA in the egg must cross over with homologous sequences in a different DNA molecule; paternal mtDNA seems the most likely candidate…. If mtDNA can recombine, irrespective of the mechanism, there are important implications for mtDNA evolution and for phylogenetic studies that use mtDNA (Morris and Mightowlers, 2000, p. 1290, emp. added). Just this past year a study was conducted that stirred these words: “Nevertheless, even a single validated example of paternal mtDNA transmission suggests that the interpretation of inheritance patterns in other kindreds thought to have mitochondrial disease should not be based on the dogmatic assumption of absolute maternal inheritance of mtDNA…. The unusual case described by Schwartz and Vissing is more than a mere curiosity” (Williams, 2002, p. 611, emp. added). And now we know that these are more than small “fractional” amounts of mtDNA coming from fathers. The New England Journal of Medicine recently noted one study in which, “[w]e determined that the mtDNA harboring the mutation was paternal in origin and accounted for 90 percent of the patient’s muscle mtDNA” (Schwartz and Vissing, 2002, p. 576). Ninety percent! And all this time we have been selectively shaping our family tree using only mothers?! As scientists begin to comprehend the finality of mitochondrial Eve, many have found themselves searching for alternatives that can maintain their beliefs on human origins. But this recombination ability in mtDNA makes the entire discussion a moot point. As Strauss noted: Such recombination could be a blow for researchers who have used mtDNA to trace human evolutionary history and migrations. They have assumed that the mtDNA descends only through the mother, so they could draw a single evolutionary tree of maternal descent--all the way back to an African “mitochondrial Eve,” for example. But “with recombination there is no
single tree,” notes Harpending. Instead, different parts of the molecule
have different histories. Thus, “there’s not one woman to whom we can
trace our mitochondria,” says Eyre-Walker (Strauss, 1999, p. 2436). Goodbye Eve. References:
* Dr. Brad Harrub serves as Director of Scientific Information, Apologetics Press. (Brad@apologeticspress.org) |
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