Mitochondrial Eve

Last updated

Haplogroup L
Early diversification.PNG
Possible time of originc. 100–230 kya [note 1] [note 2]
Possible place of originEast Africa
Ancestorn/a
Descendants Mitochondrial macro-haplogroups L0, L1, and L5
Defining mutationsNone

In human genetics, the Mitochondrial Eve (more technically known as the Mitochondrial-Most Recent Common Ancestor, shortened to mt-Eve or mt-MRCA) is the matrilineal most recent common ancestor (MRCA) of all living humans. In other words, she is defined as the most recent woman from whom all living humans descend in an unbroken line purely through their mothers and through the mothers of those mothers, back until all lines converge on one woman.

Contents

In terms of mitochondrial haplogroups, the mt-MRCA is situated at the divergence of macro-haplogroup L into L0 and L1–6. As of 2013, estimates on the age of this split ranged at around 155,000 years ago, [note 3] consistent with a date later than the speciation of Homo sapiens but earlier than the recent out-of-Africa dispersal. [4] [1] [5]

The male analog to the "Mitochondrial Eve" is the "Y-chromosomal Adam" (or Y-MRCA), the individual from whom all living humans are patrilineally descended. As the identity of both matrilineal and patrilineal MRCAs is dependent on genealogical history (pedigree collapse), they need not have lived at the same time. As of 2015, estimates of the age of the Y-MRCA range around 200,000 to 300,000 years ago, roughly consistent with the emergence of anatomically modern humans. [6]

The name "Mitochondrial Eve" alludes to the biblical Eve, which has led to repeated misrepresentations or misconceptions in journalistic accounts on the topic. Popular science presentations of the topic usually point out such possible misconceptions by emphasizing the fact that the position of mt-MRCA is neither fixed in time (as the position of mt-MRCA moves forward in time as mitochondrial DNA (mtDNA) lineages become extinct), nor does it refer to a "first woman", nor the only living female of her time, nor the first member of a "new species". [note 4]

History

Early research

Early research using molecular clock methods was done during the late 1970s to early 1980s. Allan Wilson, Mark Stoneking, Rebecca L. Cann and Wesley Brown found that mutation in human mtDNA was unexpectedly fast, at 0.02 substitution per base (1%) in a million years, which is 5–10 times faster than in nuclear DNA. [8] Related work allowed for an analysis of the evolutionary relationships among gorillas, chimpanzees (common chimpanzee and bonobo) and humans. [9] With data from 21 human individuals, Brown published the first estimate on the age of the mt-MRCA at 180,000 years ago in 1980. [10] A statistical analysis published in 1982 was taken as evidence for recent African origin (a hypothesis which at the time was competing with Asian origin of H. sapiens). [11] [12] [13]

1987 publication

By 1985, data from the mtDNA of 145 women of different populations, and of two cell lines, HeLa and GM 3043, derived from an African American and a ǃKung respectively, were available. After more than 40 revisions of the draft, the manuscript was submitted to Nature in late 1985 or early 1986 [13] and published on 1 January 1987. The published conclusion was that all current human mtDNA originated from a single population from Africa, at the time dated to between 140,000 and 200,000 years ago. [14]

The dating for "Eve" was a blow to the multiregional hypothesis, which was debated at the time, and a boost to the theory of the recent origin model. [15]

Cann, Stoneking and Wilson did not use the term "Mitochondrial Eve" or even the name "Eve" in their original paper. It is however used by Cann in an article entitled "In Search of Eve" in the September–October 1987 issue of The Sciences. [16] It also appears in the October 1987 article in Science by Roger Lewin, headlined "The Unmasking of Mitochondrial Eve". [17] The biblical connotation was very clear from the start. The accompanying research news in Nature had the title "Out of the garden of Eden". [18]

Wilson himself preferred the term "Lucky Mother" [19] and thought the use of the name Eve "regrettable". [17] [20] But the concept of Eve caught on with the public and was repeated in a Newsweek cover story (11 January 1988 issue featured a depiction of Adam and Eve on the cover, with the title "The Search for Adam and Eve"), [21] and a cover story in Time on 26 January 1987. [22]

Criticism and later research

Shortly after the 1987 publication, criticism of its methodology and secondary conclusions was published. [23] Both the dating of mt-Eve and the relevance of the age of the purely matrilineal descent for population replacement were subjects of controversy during the 1990s; [24] [25] [26] [27] Alan Templeton (1997) asserted that the study did "not support the hypothesis of a recent African origin for all of humanity following a split between Africans and non-Africans 100,000 years ago" and also did "not support the hypothesis of a recent global replacement of humans coming out of Africa." [28]

The placement by Cann, Stoneking & Wilson (1987) of a relatively small population of humans in sub-Saharan Africa was consistent with the hypothesis of Cann (1982) and lent considerable support for the "recent out-of-Africa" scenario.

In 1999, Krings et al. eliminated problems in molecular clocking postulated by Nei (1992) [29] when it was found that the mtDNA sequence for the same region was substantially different from the MRCA relative to any human sequence. [30] [31]

In 1997, Parsons et al. (1997) published a study of mtDNA mutation rates in a single, well-documented family (the Romanov family of Russian royalty). In this study, they calculated a mutation rate upwards of twenty times higher than previous results. [32]

Although the original research did have analytical limitations, the estimate on the age of the mt-MRCA has proven robust. [33] [34] More recent age estimates have remained consistent with the 140–200 kya estimate published in 1987: A 2013 estimate dated Mitochondrial Eve to about 160 kya (within the reserved estimate of the original research) and Out of Africa II to about 95 kya. [3] Another 2013 study (based on genome sequencing of 69 people from 9 different populations) reported the age of Mitochondrial Eve between 99 and 148 kya and that of the Y-MRCA between 120 and 156 kya. [2]

Female and mitochondrial ancestry

Through random drift or selection the female lineage will trace back to a single female, such as Mitochondrial Eve. In this example over five generations colors represent extinct matrilineal lines and black the matrilineal line descended from mtDNA MRCA. MtDNA-MRCA-generations-Evolution.svg
Through random drift or selection the female lineage will trace back to a single female, such as Mitochondrial Eve. In this example over five generations colors represent extinct matrilineal lines and black the matrilineal line descended from mtDNA MRCA.

Without a DNA sample, it is not possible to reconstruct the complete genetic makeup (genome) of any individual who died very long ago. By analysing descendants' DNA, however, parts of ancestral genomes are estimated by scientists. Mitochondrial DNA (mtDNA, the DNA located in mitochondria, different from the one in the cells nucleus) and Y-chromosome DNA are commonly used to trace ancestry in this manner. mtDNA is generally passed un-mixed from mothers to children of both sexes, along the maternal line, or matrilineally. [35] [36] Matrilineal descent goes back through mothers, to their mothers, until all female lineages converge.

Branches are identified by one or more unique markers which give a mitochondrial "DNA signature" or "haplotype" (e.g. the CRS is a haplotype). Each marker is a DNA base-pair that has resulted from an SNP mutation. Scientists sort mitochondrial DNA results into more or less related groups, with more or less recent common ancestors. This leads to the construction of a DNA family tree where the branches are in biological terms clades, and the common ancestors such as Mitochondrial Eve sit at branching points in this tree. Major branches are said to define a haplogroup (e.g. CRS belongs to haplogroup H), and large branches containing several haplogroups are called "macro-haplogroups".

Simplified human mitochondrial phylogeny Mitochondrial eve tree.gif
Simplified human mitochondrial phylogeny

The mitochondrial clade which Mitochondrial Eve defines is the species Homo sapiens sapiens itself, or at least the current population or "chronospecies" as it exists today. In principle, earlier Eves can also be defined going beyond the species, for example one who is ancestral to both modern humanity and Neanderthals, or, further back, an "Eve" ancestral to all members of genus Homo and chimpanzees in genus Pan . According to current nomenclature, Mitochondrial Eve's haplogroup was within mitochondrial haplogroup L because this macro-haplogroup contains all surviving human mitochondrial lineages today, and she must predate the emergence of L0.

The variation of mitochondrial DNA between different people can be used to estimate the time back to a common ancestor, such as Mitochondrial Eve. This works because, along any particular line of descent, mitochondrial DNA accumulates mutations at the rate of approximately one every 3,500 years per nucleotide. [1] [37] [note 5] A certain number of these new variants will survive into modern times and be identifiable as distinct lineages. At the same time some branches, including even very old ones, come to an end when the last family in a distinct branch has no daughters.

Mitochondrial Eve is the most recent common matrilineal ancestor for all modern humans. Whenever one of the two most ancient branch lines dies out (by producing only non-matrilinear descendants at that time), the MRCA will move to a more recent female ancestor, always the most recent mother to have more than one daughter with living maternal line descendants alive today. The number of mutations that can be found distinguishing modern people is determined by two criteria: first and most obviously, the time back to her, but second and less obviously by the varying rates at which new branches have come into existence and old branches have become extinct. By looking at the number of mutations which have been accumulated in different branches of this family tree, and looking at which geographical regions have the widest range of least related branches, the region where Eve lived can be proposed.

Newsweek reported on Mitochondrial Eve based on the Cann et al. study in January 1988, under a heading of "Scientists Explore a Controversial Theory About Man's Origins". The edition sold a record number of copies. [38]

The popular name "mitochondrial Eve", of 1980s coinage, [17] has contributed to a number of popular misconceptions. At first, the announcement of a "mitochondrial Eve" was even greeted with endorsement from young earth creationists, who viewed the theory as a validation of the biblical creation story. [39] [40] [41] [ non-primary source needed ]

Due to such misunderstandings, authors of popular science publications since the 1990s have been emphatic in pointing out that the name is merely a popular convention, and that the mt-MRCA was not in any way the "first woman". [42] Her position is purely the result of genealogical history of human populations later, and as matrilineal lineages die out, the position of mt-MRCA keeps moving forward to younger individuals over time.

In River Out of Eden (1995), Richard Dawkins discussed human ancestry in the context of a "river of genes", including an explanation of the concept of Mitochondrial Eve. [43] The Seven Daughters of Eve (2002) presented the topic of human mitochondrial genetics to a general audience. [44] The Real Eve: Modern Man's Journey Out of Africa by Stephen Oppenheimer (2003) [38] was adapted into a 2002 Discovery Channel documentary. [45]

Not the only woman

One common misconception surrounding Mitochondrial Eve is that since all women alive today descended in a direct unbroken female line from her, she must have been the only woman alive at the time. [42] However, nuclear DNA studies indicate that the effective population size of ancient humans never dropped below tens of thousands. [46] Other women living during Eve's time may have descendants alive today but not in a direct female line. [47]

Not a fixed individual over time

The definition of Mitochondrial Eve is fixed, but the woman in prehistory who fits this definition can change. That is, not only can our knowledge of when and where Mitochondrial Eve lived change due to new discoveries, but the actual Mitochondrial Eve can change. The Mitochondrial Eve can change, when a mother-daughter line comes to an end. It follows from the definition of Mitochondrial Eve that she had at least two daughters who both have unbroken female lineages that have survived to the present day. In every generation mitochondrial lineages end – when a woman with unique mtDNA dies with no daughters. When the mitochondrial lineages of daughters of Mitochondrial Eve die out, then the title of "Mitochondrial Eve" shifts forward from the remaining daughter through her matrilineal descendants, until the first descendant is reached who had two or more daughters who together have all living humans as their matrilineal descendants. Once a lineage has died out it is irretrievably lost and this mechanism can thus only shift the title of "Mitochondrial Eve" forward in time. [48]

Because mtDNA mapping of humans is very incomplete, the discovery of living mtDNA lines which predate our current concept of "Mitochondrial Eve" could result in the title moving to an earlier woman. This happened to her male counterpart, "Y-chromosomal Adam", when an older Y line, haplogroup A-00, was discovered. [49]

Not necessarily a contemporary of "Y-chromosomal Adam"

Sometimes Mitochondrial Eve is assumed to have lived at the same time as Y-chromosomal Adam (from whom all living males are descended patrilineally), and perhaps even met and mated with him. Even if this were true, which is currently regarded as highly unlikely, this would only be a coincidence. Like Mitochondrial "Eve", Y-chromosomal "Adam" probably lived in Africa. A recent study (March 2013) concluded however that "Eve" lived much later than "Adam" – some 140,000 years later. [50] (Earlier studies considered, conversely, that "Eve" lived earlier than "Adam".) [51] More recent studies indicate that Mitochondrial Eve and Y-chromosomal Adam may indeed have lived around the same time. [52]

Not the most recent ancestor shared by all humans

Mitochondrial Eve is the most recent common matrilineal ancestor, not the most recent common ancestor. Since the mtDNA is inherited maternally and recombination is either rare or absent, it is relatively easy to track the ancestry of the lineages back to a MRCA; however, this MRCA is valid only when discussing mitochondrial DNA. An approximate sequence from newest to oldest can list various important points in the ancestry of modern human populations:

See also

Phylogenetic tree of human mitochondrial DNA (mtDNA) haplogroups

  Mitochondrial Eve (L)  
L0 L1–6 
L1 L2   L3    L4 L5 L6
M N  
CZ D E G Q   O A S R   I W X Y
C Z B F R0   pre-JT   P   U
HV JT K
H V J T

Notes

  1. "the synonymous mutation rate of Kivisild et al. [...] estimates the coalescence time of the mtDNA tree overall at ~160,000 kya [...] We present a revised chronology using the complete mtDNA genome rate and an ML approach for the mtDNA tree in Figure 6, with full details of the age estimates and associated 95% confidence regions in Table S5." [1] See: Supplemental Data.
  2. "we estimate the time to the most recent common ancestor (TMRCA) of the Y chromosome to be 120 to 156 thousand years and the mitochondrial genome TMRCA to be 99 to 148 thousand years. Our findings suggest that, contrary to previous claims, male lineages do not coalesce significantly more recently than female lineages." [2]
  3. Two studies published in 2013 had 95% confidence intervals barely overlapping in the neighbourhood of 15 ka, a third study had a 95% confidence interval intermediate between the two others: "99 to 148 ka" according to Poznik, 2013 [2] (ML whole-mtDNA age estimate: 178.8 [155.6; 202.2], ρ whole-mtDNA age estimate: 185.2 [153.8; 216.9], ρ synonymous age estimate: 174.8 [153.8; 216.9]), "134 to 188 ka", according to Fu, 2013, [3] and 150 to 234 ka (95% CI) from Soares, 2009. [1]
  4. "Caution: This does not make Mitochondrial Eve the first woman, or the first human, or the first member of a new species. Further Caution: This does not mean that other women alive when Eve was do not have descendants today; they simply do not have living descendants who are descended only through female links. Yet Further Caution: If a person were to be discovered whose mtDNA showed a pattern of mutations of greater time depth, then the status of Mitochondrial Eve would be reassigned to the most recent female ancestor shared by both that person and the person we now call Mitochondrial Eve." [7]
  5. There are sites in mtDNA (such as: 16129, 16223, 16311, 16362) that evolve more rapidly, have been noted to change within intragenerational timeframes – Excoffier & Yang (1999).

Related Research Articles

In human genetics, the Y-chromosomal most recent common ancestor is the patrilineal most recent common ancestor (MRCA) from whom all currently living humans are descended. He is the most recent male from whom all living humans are descended through an unbroken line of their male ancestors. The term Y-MRCA reflects the fact that the Y chromosomes of all currently living human males are directly derived from the Y chromosome of this remote ancestor. The analogous concept of the matrilineal most recent common ancestor is known as "Mitochondrial Eve", the most recent woman from whom all living humans are descended matrilineally. As with "Mitochondrial Eve", the title of "Y-chromosomal Adam" is not permanently fixed to a single individual, but can advance over the course of human history as paternal lineages become extinct.

In biology and genetic genealogy, the most recent common ancestor (MRCA), also known as the last common ancestor (LCA), of a set of organisms is the most recent individual from which all the organisms of the set are descended. The term is also used in reference to the ancestry of groups of genes (haplotypes) rather than organisms.

The Seven Daughters of Eve is a 2001 semi-fictional book by Bryan Sykes that presents the science of human origin in Africa and their dispersion to a general audience. Sykes explains the principles of genetics and human evolution, the particularities of mitochondrial DNA, and analyses of ancient DNA to genetically link modern humans to prehistoric ancestors.

Molecular anthropology, also known as genetic anthropology, is the study of how molecular biology has contributed to the understanding of human evolution. This field of anthropology examines evolutionary links between ancient and modern human populations, as well as between contemporary species. Generally, comparisons are made between sequences, either DNA or protein sequences; however, early studies used comparative serology.

Haplogroup T is a human mitochondrial DNA (mtDNA) haplogroup. It is believed to have originated around 25,100 years ago in the Near East.

<span class="mw-page-title-main">Haplogroup N (mtDNA)</span> Widespread human mitochondrial DNA grouping indicating common ancestry

Haplogroup N is a human mitochondrial DNA (mtDNA) clade. A macrohaplogroup, its descendant lineages are distributed across many continents. Like its sibling macrohaplogroup M, macrohaplogroup N is a descendant of the haplogroup L3.

Haplogroup I is a human mitochondrial DNA (mtDNA) haplogroup. It is believed to have originated about 21,000 years ago, during the Last Glacial Maximum (LGM) period in West Asia. The haplogroup is unusual in that it is now widely distributed geographically, but is common in only a few small areas of East Africa, West Asia and Europe. It is especially common among the El Molo and Rendille peoples of Kenya, various regions of Iran, the Lemko people of Slovakia, Poland and Ukraine, the island of Krk in Croatia, the department of Finistère in France and some parts of Scotland and Ireland.

Haplogroup A is a human Y-chromosome DNA haplogroup, which includes all living human Y chromosomes. Bearers of extant sub-clades of haplogroup A are almost exclusively found in Africa, in contrast with haplogroup BT, bearers of which participated in the Out of Africa migration of early modern humans. The known branches of haplogroup A are A00, A0, A1a, and A1b1; these branches are only very distantly related, and are not more closely related to each other than they are to haplogroup BT.

Haplogroup E-M96 is a human Y-chromosome DNA haplogroup. It is one of the two main branches of the older and ancestral haplogroup DE, the other main branch being haplogroup D. The E-M96 clade is divided into two main subclades: the more common E-P147, and the less common E-M75.

<span class="mw-page-title-main">Human mitochondrial DNA haplogroup</span> Haplogroup defined by differences in human mitochondrial DNA

In human genetics, a human mitochondrial DNA haplogroup is a haplogroup defined by differences in human mitochondrial DNA. Haplogroups are used to represent the major branch points on the mitochondrial phylogenetic tree. Understanding the evolutionary path of the female lineage has helped population geneticists trace the matrilineal inheritance of modern humans back to human origins in Africa and the subsequent spread around the globe.

<span class="mw-page-title-main">Human Y-chromosome DNA haplogroup</span> Human DNA groupings

In human genetics, a human Y-chromosome DNA haplogroup is a haplogroup defined by mutations in the non-recombining portions of DNA from the male-specific Y chromosome. Many people within a haplogroup share similar numbers of short tandem repeats (STRs) and types of mutations called single-nucleotide polymorphisms (SNPs).

Haplogroup L0 is a human mitochondrial DNA (mtDNA) haplogroup.

<span class="mw-page-title-main">Haplogroup Y</span> Human mitochondrial DNA grouping indicating common ancestry

In human mitochondrial genetics, Haplogroup Y is a human mitochondrial DNA (mtDNA) haplogroup.

In human mitochondrial genetics, Haplogroup G is a human mitochondrial DNA (mtDNA) haplogroup.

Haplogroup L5 is a human mitochondrial DNA (mtDNA) clade. It was previously known as L1e.

<span class="mw-page-title-main">Haplogroup S-M230</span> Human Y-chromosome DNA haplogroup

Haplogroup S-M230, also known as S1a1b, is a Y-chromosome DNA haplogroup. It is by far the most numerically significant subclade of Haplogroup S1a.

<span class="mw-page-title-main">Macro-haplogroup L</span> Human mitochondrial lineage

In human mitochondrial genetics, L is the mitochondrial DNA macro-haplogroup that is at the root of the anatomically modern human mtDNA phylogenetic tree. As such, it represents the most ancestral mitochondrial lineage of all currently living modern humans, also dubbed "Mitochondrial Eve".

The human mitochondrial molecular clock is the rate at which mutations have been accumulating in the mitochondrial genome of hominids during the course of human evolution. The archeological record of human activity from early periods in human prehistory is relatively limited and its interpretation has been controversial. Because of the uncertainties from the archeological record, scientists have turned to molecular dating techniques in order to refine the timeline of human evolution. A major goal of scientists in the field is to develop an accurate hominid mitochondrial molecular clock which could then be used to confidently date events that occurred during the course of human evolution.

<span class="mw-page-title-main">Recent African origin of modern humans</span> "Out of Africa" theory of the early migration of humans

In paleoanthropology, the recent African origin of modern humans or the "Out of Africa" theory (OOA) is the most widely accepted model of the geographic origin and early migration of anatomically modern humans. It follows the early expansions of hominins out of Africa, accomplished by Homo erectus and then Homo neanderthalensis.

<span class="mw-page-title-main">Genetic history of the Iberian Peninsula</span> Ancestry of Spanish and Portuguese people

The ancestry of modern Iberians is consistent with the geographical situation of the Iberian Peninsula in the South-west corner of Europe, showing characteristics that are largely typical in Southern and Western Europeans. As is the case for most of the rest of Southern Europe, the principal ancestral origin of modern Iberians are Early European Farmers who arrived during the Neolithic. The large predominance of Y-Chromosome Haplogroup R1b, common throughout Western Europe, is also testimony to a sizeable input from various waves of Western Steppe Herders that originated in the Pontic-Caspian Steppe during the Bronze Age.

References

  1. 1 2 3 4 Soares P, Ermini L, Thomson N, Mormina M, Rito T, Röhl A, et al. (June 2009). "Correcting for purifying selection: an improved human mitochondrial molecular clock". American Journal of Human Genetics. 84 (6): 740–759. doi:10.1016/j.ajhg.2009.05.001. PMC   2694979 . PMID   19500773.
  2. 1 2 3 Poznik GD, Henn BM, Yee MC, Sliwerska E, Euskirchen GM, Lin AA, et al. (August 2013). "Sequencing Y chromosomes resolves discrepancy in time to common ancestor of males versus females". Science. 341 (6145): 562–565. Bibcode:2013Sci...341..562P. doi:10.1126/science.1237619. PMC   4032117 . PMID   23908239.
  3. 1 2 Fu Q, Mittnik A, Johnson PL, Bos K, Lari M, Bollongino R, et al. (April 2013). "A revised timescale for human evolution based on ancient mitochondrial genomes". Current Biology. 23 (7): 553–559. doi:10.1016/j.cub.2013.02.044. PMC   5036973 . PMID   23523248.
  4. Endicott P, Ho SY, Metspalu M, Stringer C (September 2009). "Evaluating the mitochondrial timescale of human evolution". Trends in Ecology & Evolution. 24 (9): 515–521. doi:10.1016/j.tree.2009.04.006. PMID   19682765.
  5. "New 'molecular clock' aids dating of human migration history". University of Leeds. 3 June 2009. Retrieved 23 December 2019.
  6. Karmin; et al. (2015). "A recent bottleneck of Y chromosome diversity coincides with a global change in culture". Genome Research . 25 (4): 459–66. doi:10.1101/gr.186684.114. PMC   4381518 . PMID   25770088. "we date the Y-chromosomal most recent common ancestor (MRCA) in Africa at 254 (95% CI 192–307) kya and detect a cluster of major non-African founder haplogroups in a narrow time interval at 47–52 kya, consistent with a rapid initial colonization model of Eurasia and Oceania after the out-of-Africa bottleneck. In contrast to demographic reconstructions based on mtDNA, we infer a second strong bottleneck in Y-chromosome lineages dating to the last 10 ky. We hypothesize that this bottleneck is caused by cultural changes affecting variance of reproductive success among males."
  7. "Jordan: 'Mitochondrial Eve'". weber.ucsd.edu. 2011. Retrieved 7 January 2012.
  8. Brown WM, George M, Wilson AC (April 1979). "Rapid evolution of animal mitochondrial DNA". Proceedings of the National Academy of Sciences of the United States of America. 76 (4): 1967–1971. Bibcode:1979PNAS...76.1967B. doi: 10.1073/pnas.76.4.1967 . PMC   383514 . PMID   109836.
  9. Ferris SD, Wilson AC, Brown WM (April 1981). "Evolutionary tree for apes and humans based on cleavage maps of mitochondrial DNA". Proceedings of the National Academy of Sciences of the United States of America. 78 (4): 2432–2436. Bibcode:1981PNAS...78.2432F. doi: 10.1073/pnas.78.4.2432 . PMC   319360 . PMID   6264476.
  10. Brown WM (June 1980). "Polymorphism in mitochondrial DNA of humans as revealed by restriction endonuclease analysis". Proceedings of the National Academy of Sciences of the United States of America. 77 (6): 3605–3609. Bibcode:1980PNAS...77.3605B. doi: 10.1073/pnas.77.6.3605 . PMC   349666 . PMID   6251473.
  11. Cann RL, Brown WM, Wilson AC (1982). "Evolution of human mitochondrial DNA: a preliminary report". Progress in Clinical and Biological Research. 103 Pt A (Pt A): 157–165. PMID   6298804.
  12. Cann RL, Wilson AC (August 1983). "Length mutations in human mitochondrial DNA". Genetics. 104 (4): 699–711. doi:10.1093/genetics/104.4.699. PMC   1202135 . PMID   6311667.
  13. 1 2 Cann R (May 2010). "All about mitochondrial eve: an interview with Rebecca Cann. Interview by Jane Gitschier". PLOS Genetics. 6 (5): e1000959. doi: 10.1371/journal.pgen.1000959 . PMC   2877732 . PMID   20523888.
  14. Cann RL, Stoneking M, Wilson AC (1987). "Mitochondrial DNA and human evolution". Nature. 325 (6099): 31–36. Bibcode:1987Natur.325...31C. doi:10.1038/325031a0. PMID   3025745. S2CID   4285418.
  15. Vigilant L, Stoneking M, Harpending H, Hawkes K, Wilson AC (September 1991). "African populations and the evolution of human mitochondrial DNA". Science. 253 (5027): 1503–1507. Bibcode:1991Sci...253.1503V. doi:10.1126/science.1840702. PMID   1840702.
  16. Cann RL (1987). "In Search of Eve". The Sciences. 27 (5): 30–37. doi:10.1002/j.2326-1951.1987.tb02967.x. ISSN   2326-1951.
  17. 1 2 3 Lewin R (October 1987). "The unmasking of mitochondrial Eve". Science. 238 (4823): 24–26. Bibcode:1987Sci...238...24L. doi:10.1126/science.3116666. PMID   3116666.
  18. Wainscoat J (1987). "Human evolution. Out of the garden of Eden". Nature. 325 (6099): 13. Bibcode:1987Natur.325...13W. doi: 10.1038/325013a0 . PMID   3796736. S2CID   13187170.
  19. Wilkins A (27 January 2012). "The scientists behind Mitochondrial Eve tell us about the 'lucky mother' who changed human evolution forever". Gizmodo. Retrieved 23 December 2019.
  20. Cann RL (1997). "Chapter 4: Mothers, Labels, and Misogyny". In Hager LD (ed.). Women in Human Evolution. London: Routledge. pp. 75–89. ISBN   9780415108331.
  21. Tierney J (1992). "The Search for Adam and Eve". Newsweek. Carter G. Woodson Institute for Afro-American and African Studies. Archived from the original on 20 March 2015. Retrieved 21 July 2019 via Internet Archive.
  22. Lemonick MD (26 January 1987). "Everyone's Genealogical Mother". Time. Archived from the original on 23 September 2008. Retrieved 13 May 2013.
  23. Darlu P, Tassy P (1987). "Disputed African origin of human populations". Nature. 329 (6135): 111–112. Bibcode:1987Natur.329..111D. doi: 10.1038/329111b0 . PMID   3114640. S2CID   4313392.
  24. Maddison DR (1991). "African Origin of human mitochondrial DNA reexamined". Systematic Zoology. 40 (3): 355–63. doi:10.2307/2992327. JSTOR   2992327.
  25. Nei M (November 1992). "Age of the common ancestor of human mitochondrial DNA". Molecular Biology and Evolution. 9 (6): 1176–1178. doi: 10.1093/oxfordjournals.molbev.a040785 . PMID   1435241.
  26. Ayala FJ (December 1995). "The myth of Eve: molecular biology and human origins". Science. 270 (5244): 1930–1936. Bibcode:1995Sci...270.1930A. doi: 10.1126/science.270.5244.1930 . PMID   8533083. S2CID   42801341.
  27. Templeton A (March 2002). "Out of Africa again and again". Nature. 416 (6876): 45–51. Bibcode:2002Natur.416...45T. doi:10.1038/416045a. PMID   11882887. S2CID   4397398.
  28. Templeton AR (December 1997). "Out of Africa? What do genes tell us?". Current Opinion in Genetics & Development. 7 (6): 841–847. doi:10.1016/S0959-437X(97)80049-4. PMID   9468796.
  29. Nei M (1992). "Age of the common ancestor of human mitochondrial DNA". Molecular Biology and Evolution. 9 (6): 1176–1178. doi: 10.1093/oxfordjournals.molbev.a040785 . PMID   1435241.
  30. Krings M, Salem AE, Bauer K, Geisert H, Malek AK, Chaix L, et al. (April 1999). "mtDNA analysis of Nile River Valley populations: A genetic corridor or a barrier to migration?". American Journal of Human Genetics. 64 (4): 1166–1176. doi:10.1086/302314. PMC   1377841 . PMID   10090902.
  31. Krings M, Stone A, Schmitz RW, Krainitzki H, Stoneking M, Pääbo S (July 1997). "Neandertal DNA sequences and the origin of modern humans". Cell. 90 (1): 19–30. doi: 10.1016/S0092-8674(00)80310-4 . hdl: 11858/00-001M-0000-0025-0960-8 . PMID   9230299. S2CID   13581775.
  32. Parsons TJ, Muniec DS, Sullivan K, Woodyatt N, Alliston-Greiner R, Wilson MR, et al. (April 1997). "A high observed substitution rate in the human mitochondrial DNA control region". Nature Genetics. 15 (4): 363–368. doi:10.1038/ng0497-363. PMID   9090380. S2CID   32812244.
  33. Holsinger K (29 September 2012). "(Mathematics of the coalescent) An example: Mitochondrial Eve". Holsinger Lab. Retrieved 16 May 2013.
  34. Cyran KA, Kimmel M (November 2010). "Alternatives to the Wright-Fisher model: the robustness of mitochondrial Eve dating". Theoretical Population Biology. 78 (3): 165–172. doi:10.1016/j.tpb.2010.06.001. PMID   20600209.
  35. Giles RE, Blanc H, Cann HM, Wallace DC (November 1980). "Maternal inheritance of human mitochondrial DNA". Proceedings of the National Academy of Sciences of the United States of America. 77 (11): 6715–6719. Bibcode:1980PNAS...77.6715G. doi: 10.1073/pnas.77.11.6715 . PMC   350359 . PMID   6256757.
  36. Birky CW (August 2008). "Uniparental inheritance of organelle genes". Current Biology. 18 (16): R692–R695. doi: 10.1016/j.cub.2008.06.049 . PMID   18727899. S2CID   9866662.
  37. Gibbons A (January 1998). "Calibrating the mitochondrial clock". Science. 279 (5347): 28–29. Bibcode:1998Sci...279...28G. doi:10.1126/science.279.5347.28. PMID   9441404. S2CID   29855766.
  38. 1 2 Oppenheimer S (2003). The Real Eve: Modern Man's Journey Out of Africa. New York: Basic Books. ISBN   978-0-7867-1192-5.
  39. Wieland C (2005). "Mitochondrial Eve and biblical Eve are looking good: criticism of young age is premature". Journal of Creation. 19 (1): 57–59.
  40. Nelson CW (1 April 2003). "Genetics and Biblical Demographic Events". Answers in Genesis . Retrieved 16 May 2013.
  41. Oakes J (25 January 2007). "Can the human arguments about mitochondrial Eve and y-chromosome Adam be extended to the animal world to test the reality of the flood of Noah?". Evidence for Christianity. Answers in Genesis. Retrieved 16 May 2013.
  42. 1 2 Dawkins R (2004). The ancestor's tale: a pilgrimage to the dawn of evolution. Boston: Houghton Mifflin. ISBN   978-0-618-00583-3.
  43. Dawkins R (1995). River out of eden: a Darwinian view of life. Basic Books. ISBN   978-0-465-06990-3 . Retrieved 5 December 2011.
  44. Sykes B (2002). The Seven Daughters of Eve: The Science That Reveals Our Genetic Ancestry . W. W. Norton & Company. ISBN   978-0-393-32314-6.
  45. Oppenheimer, Stephen (2003). The Real Eve: Modern Man's Journey Out of Africa. Carroll & Graf. ISBN   978-0-7867-1192-5.
  46. Takahata N (January 1993). "Allelic genealogy and human evolution". Molecular Biology and Evolution. 10 (1): 2–22. doi: 10.1093/oxfordjournals.molbev.a039995 . PMID   8450756.
  47. "Are we all descended from a common female ancestor?". HowStuffWorks. 14 January 2008. Retrieved 17 May 2022.
  48. Learn JP. "No, a Mitochondrial 'Eve' Is Not the First Female in a Species". Smithsonian Magazine. Retrieved 23 February 2021.
  49. Mendez FL, Krahn T, Schrack B, Krahn AM, Veeramah KR, Woerner AE, et al. (March 2013). "An African American paternal lineage adds an extremely ancient root to the human Y chromosome phylogenetic tree". American Journal of Human Genetics. 92 (3): 454–459. doi:10.1016/j.ajhg.2013.02.002. PMC   3591855 . PMID   23453668.
  50. Barras C (6 March 2013). "The father of all men is 340,000 years old". New Scientist. Retrieved 13 March 2013.
  51. Cruciani F, Trombetta B, Massaia A, Destro-Bisol G, Sellitto D, Scozzari R (June 2011). "A revised root for the human Y chromosomal phylogenetic tree: the origin of patrilineal diversity in Africa". American Journal of Human Genetics. 88 (6): 814–818. doi:10.1016/j.ajhg.2011.05.002. PMC   3113241 . PMID   21601174.
  52. Callaway E (6 August 2013). "Genetic Adam and Eve did not live too far apart in time". Nature. doi:10.1038/nature.2013.13478. S2CID   170608686.
  53. 1 2 Rohde DL, Olson S, Chang JT (September 2004). "Modelling the recent common ancestry of all living humans". Nature. 431 (7008): 562–566. Bibcode:2004Natur.431..562R. CiteSeerX   10.1.1.78.8467 . doi:10.1038/nature02842. PMID   15457259. S2CID   3563900.
  54. Zhou, Jin; Teo, Yik-Ying (August 2016). "Estimating time to the most recent common ancestor (TMRCA): comparison and application of eight methods". European Journal of Human Genetics. 24 (8): 1195–1201. doi: 10.1038/ejhg.2015.258 . ISSN   1476-5438. PMC   4970674 . PMID   26669663. S2CID   965600.

Further reading

Listen to this article (9 minutes)
Sound-icon.svg
This audio file was created from a revision of this article dated 22 April 2005 (2005-04-22), and does not reflect subsequent edits.