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Playing Favorites: Two Illustrations of Rushton’s
Genetic Similarity Theory
Can humans distinguish
subtle genetic differences, even within the immediate family?
Apparently, grandmothers can do so, as
explained in Molly Fox, et al.,
Grandma plays favourites: X-chromosome
relatedness and sex-specific childhood mortality, published in
Proceedings of the Royal Society B, in
October of last year.
The “grandmother
hypothesis” has been invoked to explain why women live several decades past the
end of their reproductive years.
Older, post-menopausal women can enhance their biological fitness by
contributing to the survivability of their grandchildren, since there is
significant genetic relatedness between grandparent-grandchildren.
Thus, the grandmother hypothesis suggests that a long post-reproductive
lifespan for human women evolved because of the adaptive value of assisting in
the care of their children’s children.
However, due to the
specific mechanisms of the inheritance of the sex chromosomes, the genetic
relatedness of grandmother to grandchild will differ depending on whether the
grandchild is a boy or a girl, and whether the grandmother is the paternal
grandmother (father’s mother) or maternal grandmother (mother’s mother).
Let me explain.
Girls have two X
chromosomes, one from the mother and one from the father, while boys have one X
chromosome (from the mother) and one Y chromosome (from the father).
These X and Y chromosomes are, in turn, inherited from the grandparents.
Let us consider a maternal grandmother. She has two X chromosomes. One of these two X’s will be passed on to her daughter (the mother); thus the probability that any specific X chromosome gene will be passed from maternal grandmother to mother is 0.5. (See Figure.)

The figure shows that a paternal grandmother (PGM)
is more closely related to her granddaughter because the granddaughter carries a
more or less exact replica of one of her X Chromosomes (the blue X chromosome in
the figure) while her grandson carries neither or her X Chromosomes.
Theoretically, she should prefer her granddaughter to her grandson. The maternal
grandmother (MGM) is equally related to grandson and granddaughter, so she
should not show favoritism. The chromosomes with red and black parts result from
recombination (crossover) during meiosis.
The mother has two X
chromosomes herself, so the probability of the mother passing any specific X
chromosome gene to either a boy or a girl child is likewise 0.5.
Therefore, the probability of any specific X chromosome gene being passed
on from a maternal grandmother to a grandchild is 0.25 (0.5 x 0.5).
From the standpoint of the maternal grandmother, there is no difference
between grandson and granddaughter in X-chromosome relatedness and, hence,
approximate overall genetic relatedness.
The situation is markedly
different for a paternal grandmother,
the mother of the grandchildren’s father.
Again, she has two X chromosomes, one which can be passed on to her son
(the father); thus, there is a 0.5 chance of any X-chromosome gene being passed
from paternal grandmother to father. However,
the father has only that one X chromosome to be passed on to his own children.
If he has a girl (granddaughter), there is a probability of 100% (1.0)
that his X chromosome is passed on to his daughter; therefore, one of the two X
chromosomes in that girl must be
derived from the paternal grandmother.
What about the grandson of
a paternal grandmother? His only X
chromosome comes from his mother, not his father.
Therefore, the paternal grandmother does not contribute an X chromosome
to a grandson, implying an X-chromosome relatedness of 0.
Therefore (and this is the
important point), a paternal grandmother, all else being equal, is genetically
less related to a grandson than to a granddaughter, and less related to a
grandson than is a maternal grandmother.
Conversely, a paternal grandmother likely is more genetically related to
a granddaughter than is a maternal grandmother, given the certainty that the
granddaughter possesses an X chromosome from the paternal grandmother.
Further, genetic
recombination between the X and Y chromosomes in the formation of sperm is very
limited, meaning that a granddaughter inherits from her paternal grandmother a
more or less “intact” X chromosome. On the other hand, the X chromosome
inherited from the maternal grandmother will contain some amount of genes from
the maternal grandfather,
due to the extensive recombination between X chromosomes that occurs during the
formation of the human egg.
The bottom line is that
the highest degree of genetic relatedness is most likely to be between paternal
grandmother and granddaughter, the least between paternal grandmother and
grandson, with maternal grandmother-grandchildren exhibiting more intermediate
levels of relatedness. (See Figure above.)
The authors of this study
hypothesized that grandmothers’ investment in their grandchildren would mirror
the relative genetic relatedness.
They analyzed the effect of the presence of paternal or maternal grandmothers,
in the grandchildren’s household or in the grandchildren’s village, to childhood
survivability/mortality. The data
were obtained from seven populations: Japan, Germany, England, Ethiopia, The
Gambia, Malawi, and Canada dating in some cases as far back as the 17th
century (when available) and extending to the 21st century.
The findings are
remarkable. The presence of the
paternal grandmother was detrimental to the survivorship of grandsons.
In six out of the seven populations (Gambia being the exception) the
presence of the paternal grandmother was better for girls than for boys.
In all populations, boys survived better with the maternal, as opposed to
the paternal, grandmother; in four out of the seven populations, girls survived
better with the paternal, as opposed to the maternal, grandmother.
The findings essentially support the authors’ fundamental hypothesis.
What can be the mechanism
behind this phenomenon? Here the
authors speculate that a “behavioral adaption” may cause women to favor
grandchildren of a specific sex; alternatively, the grandchildren may be sending
out “signals” that represent relative genetic relatedness (e.g., physical
resemblance, pheromones, etc.).
The authors unfortunately
tend to dismiss a behavioral mechanism based upon negative results of
“questionnaires” that did not observe a relationship between preferential care
and genetic relatedness. However, in my opinion, these sorts of social science
analyses are very weak and highly dependent upon the types of questions asked
and the honesty of those answering the questions.
The authors instead
propose a purely genetic explanation in that genes related to phenotypes
influencing fitness are likely found on the X chromosome and thus variation in
the inheritance of these genes between grandmother and grandchild can influence
survivability. For example, if the
paternal grandmother carries particularly helpful genes on her X chromosome,
these would be present in the granddaughter, enhancing survivability, and absent
in the grandson, depressing survivability.
However, this explanation, and the related one involving “epigenetic
modifications” of X chromosome genes inherited from the paternal grandmother to
granddaughter, do not explain why the
presence of one or the other grandmother should have such a marked effect on
childhood outcomes and why the presence
of the paternal grandmother actually seems detrimental to grandson
survivability.
I believe that the social
science “questionnaire data” do not eliminate the possibility of a behavioral
mechanism predicated on the ability of the grandmothers to somehow become aware
of the differing levels of genetic relatedness of the grandchildren.
I do not suggest any sort of conscious activity — “that grandson of mine
is less related to me than his sister, so I’ll ignore him and help her.”
On the contrary, similar
to J.P Rushton’s “genetic
similarity theory” (GST) of which this phenomenon is likely a variant,
the grandmothers’ perception of genetic relatedness is probably more on the
unconscious level; there is a greater attraction to and affinity for the more
genetically related paternal granddaughter, resulting in a greater investment.
Likewise, there may be a subconscious aversion towards a paternal grandson which
results in a more careless attitude toward care and provisioning.
Averaged over large numbers of people, these subtle differences in
behavior would result in variant levels of childhood survivorship vs. mortality.
How exactly the genetic differences are being unconsciously detected is
as yet unknown.
Related to this, and also
likely associated with GST, is a fascinating analysis from the laboratory of
Neil Risch, who is one of the few population geneticists honest about the
biological reality of race (Risch
et al., Ancestry-related assortative mating in Latino populations,
Genome Biology, doi:
10.1186/gb-2009-10-11-r132).
Risch and colleagues set out to determine whether there was any correlation
between the ancestral proportions of spouses in either Mexican or Puerto Rican
populations. Assortative mating
(like with like) is a proven phenomenon, based on a number of characteristics,
including physical appearance, behavior, and other biological attributes.
Hispanic populations are well suited for analyzing whether genetic
ancestry influences mate choice, since “Latino” groups are heavily admixed and
exhibit a wide range of ancestries within single ethnic-national-cultural
groups. Both Mexicans and Puerto
Ricans are significantly triracial (European-sub-Saharan African-Amerindian),
with Mexicans characterized by greater Amerindian and minor African admixture,
and Puerto Ricans by significant African and somewhat lower, but still
significant, Amerindian ancestry.
Socioeconomic status (SES) and geographical origin (Mexico/Puerto Rico or the
USA) of the study participants was controlled for, strengthening the findings.
Risch
et al. discovered was that among
Mexicans there is a strong correlation between spousal European and Native
American, but not African, ancestry; in other words, Mexican husbands and wives
are well matched in percent European and Native American ancestry, significantly
beyond random chance. African
ancestry does not correlate significantly in Mexican spouses.
For Puerto Ricans, the spousal correlations were significant for European
and African, but not Amerindian, ancestry.
It seems that Mexicans are
somehow gauging the Amerindian admixture in their potential mates, while Puerto
Ricans concentrate on matching levels of African ancestry.
Analysis of the
distribution of gene alleles within and between individuals strongly suggests
that this “like with like” mating has been going on for quite some time, and
possibly was more pronounced in previous generations than today.
Given that SES and geographical origin do not seem to play any roles in
markers of ancestry, what is the mechanism by which this assortative mating
takes place?
Obviously, physical
features can serve as a proxy for ancestry; therefore, perhaps, Latinos are
hooking up with each other based upon who “looks Whiter” or “looks more
Amerindian or African.” However, the
authors note that to achieve the fairly high correlations of husband-wife
ancestry, a very marked association between physical traits and genetic
ancestral proportions is required.
The problem is that previous studies of Latin American groups have not shown
genotype-phenotype associations of the required levels.
Therefore, it is unlikely that physical appearance alone can suffice as
an explanation.
Perhaps a number of
different factors, including appearance, acting in concert can have a
synergistic effect on ancestral identification for assortative mating.
One must remember that a number of “Latino” cultures have historically
prized higher degrees of White ancestry, and perhaps older family members
“advertise” their “whiteness” so as to attract the “right sort” of mates for the
younger generation.
Both the grandmother and
Latino assortative mating stories are of relevance to us because they describe
real-life examples of GST-like behavior. They show the ability of individuals
to, at some level, recognize relative differences in genetic similarity.
This obviously has bearing
on the recognition of ethnic kin in multiracial, multicultural societies, and
the propensity to favor such kin, either consciously or unconsciously.
One may speculate that if people can perceive relative genetic ancestry
via some sets of cues, and if this influences behavior, then this may explain
some of the costs of diversity, including lower levels of societal investment.
Indeed, given that these
studies suggest the ability to distinguish genetic differences even within
immediate families, it is plausible that differences in ethnic kinship within
single ethnic groups can determine societal harmony and progress.
For example, one would expect that ethnic-national groups that are
relatively genetically homogenous would exhibit higher degrees of investment in
collective goods, such as public health insurance. On the other hand,
ethnic-national groups that are more genetically heterogeneous, for whatever
reason, would exhibit less societal investment and more focus on the family unit
and extended kin relationships.
The possibility that
relative genetic homogeneity could be part of the explanation for differences in
social structure and public goods investment in different European nations is a
provocative hypothesis. It is also
possible that different ethnic and racial groups exhibit these sorts of
behaviors to different degrees; more ethnocentric peoples may be better at
detecting subtle differences in genetic kinship than those who are more
tolerant.
And what if the mechanism
behind the Fox and Risch findings is discovered?
Will those opposed to our people’s survival attempt to find ways of
short-circuiting this mechanism, perhaps even to misdirect it so as to make
Westerners favor aliens over kin to an even greater extent than they already do?
Conversely, can we use these discoveries to our advantage?
Only time will tell.
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