How Small Genetic Differences Give Racial Divergency
Report; Posted on: 2005-11-02 14:07:40
DNA - building brick of life
by John Bean
When the Human Genome Project was completed in 2000, it was widely touted that its result showed no genetic basis for race. In fact some scientists of the liberal-left consensus went so far as to dub race a “biological fiction”. Developments since then have clearly demonstrated that quite small genetic differences can produce disproportionate results that substantiate the fact that racial differences are a reality and that they are more complex than just differences in skin colour and hair texture.
When we are told that as the difference in DNA between peoples from different parts of the globe is so small therefore there is really no such thing as ‘race’, let us first remember that the difference between humans and chimpanzees is only just over one per cent. Yet despite sharing 99 per cent of the same DNA how is it that we are so different in appearance, behaviour and, above all, in mental abilities? Our pet dogs and cats also share around 80 per cent of our DNA. Approximately 75 per cent of mouse genes so far identified have a firm counterpart in the human genome.
Furthermore, according to Prof Stylianos Antonarakis of the University of Geneva Medical School and Dr Ewen Kirkness of the Institute of Genomic Research, Maryland, latest DNA research shows that some DNA regions of humans, dogs, and species as distant as elephant and wallaby are nearly identical. 2 Importantly, they also found that huge tracts of human DNA, previously written off as meaningless junk, have been found to contain a hitherto unrecognised “genetic grammar”, making the language of our genes much more complex than previously thought. More on the importance of this DNA junk in carrying group, or racial, differences later. But for the moment let it be noted that small though DNA differences may be the effects they can have are considerable.
It starts In Your Genes
We appreciate that for some readers we may be preaching the art of egg-sucking for grandmothers. For those who have not really bothered about ‘genes’, ‘chromosomes’ and DNA, the following is a basic guide suitable for anyone with O level Science.
The characteristics you inherit from your parents and other ancestors are in your inherited genes. This genetic information forms part of the chromosomes which are carried in DNA, which is a chemical called deoxyribonucleic acid... The chromosomes, which exist in pairs, are threadlike structures, usually found in the cell nucleus of animals and plants carrying the genes. The DNA molecule takes the structure of a double helix, i.e. a pair of parallel helixes with a common axis, and it exists in the nucleus of every living cell. This was the revolutionary discovery made by the British scientists James Watson and Francis Crick in 1953, including the fact that the two strands were complementary. The complete DNA sequence housed in a cell of an organism is known as its genome.
DNA consists of long sequences of four chemical ‘letters’ – C,T,G, and A – strung together in different combinations like different coloured beads on a necklace 2. The information of DNA is encoded in the precise order of these four chemicals; like writing but using fewer symbols.
Genes are the smallest element of DNA and are the basis of heredity. There are many thousands of genes that create each chromosome. In the human body there are 46 pairs of chromosomes. They are sections of data that is received from our parents; one chromosome from each parent and they combine in the embryo to create a set. It was originally thought that the genetic message comes equally from each parent, but it now seems that some children might end up with three, four or even more copies of a gene from one parent. Although one can often see that offspring are related, even with large families each child, unless an identical twin, will be different in varying degrees. This is because the number of different offspring a pair of human parents could produce are to the power of 47 (remember there are 46 pairs of chromosomes that can be shuffled about) or 140,000,000,000,000.
It is the nuclear DNA that really makes us what we are. It consists of around 25,000 genes, compared with a paltry 37 that our mothers pass to us in mitochondria.
Mitochondria are the powerhouse of the cell. They consume the sugars that our bodies have converted from food and in return produce electricity with which to power the cell But it is considered to be separate from the cell, because it has its own DNA, and this DNA is unaffected by other genetic exchanges.
Although you may have inherited all manner of characteristics through your nuclear DNA from parents, grandparents and back many generations, there is one factor that remains constant: the mitochondrial DNA hasn’t altered at all. It remains intact through the female line. Male sperm contains only enough mitochondria to power the sperm to the surface of the egg – it does not enter the egg. The egg, however, contains mitochondria that have been passed from mother to daughter for countless generations. The only way for mitochondrial DNA to alter is by natural mutations, which occur very slowly when compared with the almost frantic gene mixing we and our parents take part in. Importantly, according to Adrian Woolfson 1 even the smallest DNA changes can result in significant changes to the structure and function of a living creature. In fact minute changes can have disproportionate results. It is this natural mutation of mitochondrial DNA occurring just occasionally over countless generations that has led to group differences and thereby the establishment of separate human races.
Because the rate of mitochondrial genetic mutation is slow it can be used as a clock to turn back time to a period before the mutations had crept in. The common belief at present is that modern Europeans originated from Africa (although some, such as Prof. Carleton S.Coon contend that homo sapiens evolved in several global areas). When mitochondrial DNA from modern sub-Saharan African populations are sampled they can be compared with European mitochondrial DNA. The mutation difference between the two populations can then be compared and a ‘clock’ can be produced to give a time-scale which indicates when modern Europeans first left Africa (assuming they did).
Another aspect of the slowness of mitochondrial genetic mutation is that the study of DNA samples from human skeletal remains (based on a branch of science known as ‘archeogenetics’) showed that the first human settlers arrived in Britain around 12000 BC as Britain was thawing from the last ice age. They were from what is now known as Western Germany, the Netherlands and Denmark. According to David Miles, formerly chief archaeologist at English Heritage and a research fellow at Oxford University 3 in his book, The Tribes of Britain, the genetic make-up of modern white indigenous Britons has hardly changed from those first Ice Age arrivals. He states that 80 per cent of the average white British person shares the same genetic characteristics as those early nomads.
Some nationalists have misinterpreted this important information by suggesting that the Anglo-Saxons and Vikings, and even the Celts, must have had a minimal racial contribution to white British stock if 80 per cent of us share the same genes as the first arrivals of 12000BC. The point here is that all these people were but different tribes of a common race (the first known homeland of the Celts was in Southern Germany) which once stretched from the Urals to the Atlantic north of the Alps, and were found even in modern day Turkey and Iraq. Genetic testing has been carried out on modern day white Danes, Dutchmen and Germans from Saxony and in nearly all cases no difference in DNA has been found.
Small Differences – Wide Ranging Results
The human DNA carries an estimated 25,000 genes and not much more than 0.1 per cent, i.e. 320 genes, account for the differences between individuals and races, whether it be freckles, Afro hair, ginger hair or hereditary in-growing toenails. Geneticist Steve Scherer, a senior scientist at Toronto’s Hospital for Sick Children, has said: “Based on what we now know it (the genetic difference) is probably in the 0.2 per cent range and in the end it may even be as high as one per cent.”4
Within the last five years scientists have carried out in-depth work to chart these genetic variations. One of these, Francis, a former leader of the Human Genome Project, had to admit that “well-intentioned statements” about the biological insignificance of race may have left the wrong impression: “It is not strictly true that race or ethnicity has no biological connection”.5
Again, the importance of the small genetic differences between people groups/races was suggested in a paper this year by Hua Tang and other scientists on “Genetic Structure, Self-Identified Race/Ethnicity”. 6 Hua Tang et al contended that in a study of Blacks, Whites, Hispanics and Asians in 12 different U.S. locations and three in Taiwan, that there are 326 genetic markers on racial differences.
A variation in a single gene may explain why some people can withstand pain – or other physical or emotional stress – better than others, a team from the University of Michigan and the National Institutes of Health reported in a recent issue of Science.
If we bear in mind that flies and worms have around half as many genes as humans and that fish, rats and mice have almost the same number as us, then it cannot be genes alone that account for the differences between us. As Woolfson explains 1, the main difference between the genes of ‘higher’ organisms, such as vertebrates, and those of ‘lower’ organisms is that they are ‘smarter’., which means simply that each gene is more complex, as are its behavioural patterns. As genes become smarter, the organisms they build and operate become more complex.
We also have to consider that as much as 98% of the human genome contains ‘junk’, which are DNA sequences that lack protein-coding genes and about which scientists still need to know much more. It is now being found that a huge amount of information lies outside genes, scattered throughout the ‘junk’ and is responsible for the maintenance, regulation and reprogramming of genetic processes.
Now pulling all the above information together, it can be seen, for example, that the difference between the complexity of a fly and a human can be explained not only by the extra 10,000 or so genes found in a humans, but in the number of different gene behavioural patterns each genome is capable of producing. The difference is a huge number, larger than the number of elementary particles in the known universe, according to Woolfson 1. This means that a relatively small variation in the number of genes between two species has the potential to generate a tremendous difference in biological complexity.
If one applies this to the 300 plus gene differences between, for example, the European and the African, it would explain the biological, physical and metaphysical differences between these two races of the common species homo sapiens.
Several laboratory investigations carried out on behalf of the Police and/or the FBI in the USA have confirmed that genetic testing can determine a persons exact racial profile. A classic report was that by Josh Noel, a staff writer for the the Advocate News, Florida, 06/04/03.
“A private genetics lab altered the hunt for the south Louisiana serial killer after telling investigators that the person they sought was a black man. For eight months the investigation had focussed on white men.
“Tony Frudakis, chief executive officer of DNAPrint Genomics said that he told the task force that the serial killer was 85% Sub-Saharan and 15% Native American based on analysis of the killer’s DNA.”
Eventually a black man was arrested as his DNA matched exactly the lab’s report. Frudakis has said his company can determine a person’s ancestral past by analysing 73 DNA markers and narrowing the result to proportions in four categories: East Asian, Indo-European, Native American and Sub-Saharan African.
The Guardian, 16/06/05, reported that a drug (BiDil) was now available in America which was aimed specifically at African-Americans to remedy heart failure. Among New Yorkers aged 45 to 54 the death rate from heart disease among black people is 55% higher than among whites. The Food & Drug Authority’s stamp of approval for the drug was being opposed by some liberals because it would “give the stamp of authority on racial biological differences”.
In an article on genetic medicines in The Times, 18/6/05, Kenan Malik said that according to the American Heart Association the death rate amongst Black Americans was five times that of Whites. Malek also pointed out that Northern Europeans are more likely to suffer from cystic fibrosis than other groups. Tay-Sachs, a fatal disease of the central nervous system, particularly affects Ashkenazi Jews. Beta-blockers appear to work less effectively for African-Americans than those of European descent.
The New Scientist, 20/1/05 reported that a length of DNA has been found in a fifth of Europeans which is very rare in Africans and non-existent in Asians. This DNA is said to be 3 million years old and can only have passed to modern Europeans in the last 50,000 years, otherwise it would be present today in all other races.
In 1992 Bo Rybeck, Director of the Swedish National Defence Research Institute, stated that as we became able to identify the DNA variations of different races and ethnic groups, we will be able to determine the difference between blacks and whites and Orientals and Jews and Swedes and Finns and develop an agent that will kill only a particular group.”
The Sunday Times, 15.11.1998, revealed in a report from Israel : “Israel is working on a biological weapon that would harm Arabs but not Jews, according to Israeli military and western intelligence sources. In developing their ‘ethno-bomb’, Israeli scientists are trying to exploit medical advances by identifying genes carried by some Arabs.”
A North Korean team of microbiologists are also said to be working on an ethno-bomb which would destroy white races.
Before the secrets of DNA began to be unravelled and showed clearly that there were many genetic markers indicating racial differences, ample evidence had existed but was ignored or suppressed by the Marxist-liberal intellectual ‘elite’ and its media mouthpieces. All differences were due to environmental factors, they said. This was the standard answer to the findings of countless IQ tests over the past century which have consistently shown that Eastern Asians (Chinese, Koreans, Japanese) have a higher IQ than Europeans, who in turn are some 15 % above people of African origin. The most in-depth investigation into IQ was probably that carried out by Herrnstein and Murray, the results of which were published in The Bell Curve, 1994, and greeted in the main with abuse by those who could not challenge their findings on racial IQ differences and that it was largely genetic and hereditary.
This may be connected with the fact that the Sub-Saharan African has a brain weighing just under 1 kg, compared with 1240 gms for Europeans and 1300 gms for East Asians.
We are frequently told that there is a shortage of West Indian, African and Asian blood donors in the UK, but at the same time we are told there is no difference in the ratio of the blood groups in the various racial groupings. Similarly, with kidney, heart and other organ transplants emphasis is given to matching the race of the donor and the recipient. More recently doctors have found, to their apparent surprise, that this also applies to the success of bone marrow transplants.
It has long been known that West Indians and African are almost exclusively susceptible to the hereditary blood characteristic, sickle cell anaemia. This makes them more receptive to jaundice, pneumonia and TB, sometimes leading to death.
The UK Prostate Cancer Charity issued a report in March 2005 that Prostate cancer among African Caribbean men is three times more prevalent than among whites. American Indians have a tendency to hypertension and high blood pressure and, like the Japanese, have a low tolerance to alcohol.
We could probably continue with another page of specific biological, physical and mental differences to support our view that all these minor differences add up to there being a substantial difference between the world’s main races. However, the emphasis is on difference, not on superiority of any one race over another because it would depend on the yardstick chosen to do this.
To end on a personal note, the human genome project revealed that there are some 1400 potential illnesses/diseases carried by single gene markers, and one of them I suffer from. This is Dupuytren’s Contracture, which causes one or more fingers to bend in towards the palm; a ‘disease’ which I shared with Margaret Thatcher. Prior to an operation my surgeon said that it only occurs among people of “North European descent” and is sometimes known as the “Scandinavian disease”. The highest rates of incidence world-wide are in Iceland, followed by Denmark, and in Britain, the Orkneys and Shetlands followed by the north east of England (where many of my ancestors came from). Of course, distorted fingers are of little concern for the future of the world’s races, but distorted reporting on the genetic evidence of each race’s distinctiveness is of great concern.
1. Adrian Woolfson, An Intelligent Person’s Guide to Genetics, published by Duckworth Overlook, London, 2004.
2. Science, October 2003.
3. David Miles, The Tribes of Britain, Oxford University Press
4. Paper by Professor Henry Harpending, University of Utah, June 2005.
5. Nature Genetics, Autumn 2004
6. American Journal of Human Genetics, Spring 2005
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