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Science Friday
Women's chromosome division different from men's
Error more likely as human eggs prepare genetic material
Web edition : Wednesday, November 12th, 2008
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A HUMAN OOCYTEA human oocyte in meiosis. Protein complexes that bind homologous (partner) chromosomes are shown in red, proteins that mark sites of cross-overs are in yellow, and proteins associated with centromeric regions are in blue. Other "splashes" of color come from DNA probes that recognize specific human chromosomes.Hassold, et al.

PHILADELPHIA — Women and men sometimes do things differently, right down to divvying up their genetic legacies.

This divvying up is known as meiosis, a process that cuts the number of chromosomes in half during the production of eggs and sperm. Men do meiosis by the textbook, but women play it looser with the process, scientists from Washington State University and the University of Washington reported Nov. 12 in Philadelphia at the annual meeting of the American Society of Human Genetics.

The finding could help explain why women sometimes pass along the wrong number of chromosomes to their children, the researchers suggest. “The male doesn’t contribute to chromosome abnormality in any way,” says Terry Hassold, a geneticist at Washington State University in Pullman who presented the findings.

Some genetic disorders, such as Down syndrome, are caused by having an extra copy of a chromosome. Humans normally have two copies of each chromosome, one inherited from mom and one from dad. About one in every 700 babies born has an extra copy of chromosome 21, a surplus that causes Down syndrome. About one in every 1,000 babies born may have an extra X or Y chromosome, and one in every 1,000 girls may have only one X chromosome. Abnormalities in the number of other chromosomes often lead to miscarriage or to death soon after birth.

Humans are the only species known to have a high rate of error in the number of chromosomes they pass along, Hassold says. About 25 percent of all fertilized human eggs have the wrong number of chromosomes, he says.

“It’s a major problem and it’s only getting worse” as more older women have children, he adds. Such genetic mistakes happen more often after about age 35.

Hassold and colleague Edith Cheng from the University of Washington in Seattle decided to examine human meiosis to find a possible source for the high rate of error.

Fluorescent antibodies that latch on to proteins involved in meiosis allowed the researchers to see how the process happens. Hassold and his colleagues had already examined the earliest phase of meiosis in men and found that it follows the steps laid out in every biology textbook: a chromosome finds its match and the two pair up, gluing themselves together. Then the chromosomes swap some genetic information, a process known either as recombination or crossing over. Next, the chromosomes go through two rounds of division to form four sperm, each with one copy of each chromosome.

Previously, scientists did not have the tools to study human meiosis the way Hassold and Cheng have, says Stephen Warren, a human geneticist at Emory University in Atlanta. The new results provide insight about why humans tend to have higher rates of chromosomal mistakes, but the data fail to account for a large number of recombination events that scientists know must happen, he says.

Women may use more than one system for recombination, only one of which is visible using the technique in the new study, Warren speculates.

While still in the womb, female embryos accumulate all of the eggs they will ever have. Each cell is in a state of suspended animation until it is released, some time between puberty and menopause, making a mature egg. Some eggs might remain on hold for more than 40 years.

That suspended animation was known, but Hassold and Cheng found that, in addition, women’s chromosomes don’t behave the way men’s do.

In men, chromosome pairs zip themselves tightly together all along their length. But in women, Hassold saw “split ends” and “bubbles” where the chromosomes were not tightly joined. And women’s chromosomes had fewer recombination points than expected. About 5 percent of the chromosome 21 pairs the researchers examined had no evidence of recombination.

Recombination is necessary for proper chromosome segregation so failure to cross over could account for some of the errors in women, including passing along the wrong number of chromosomes.

The error-prone recombination process in women may have some evolutionary advantage, the researchers say, but they don’t know yet what that might be.

Warren suggests that one advantage of high rates of chromosomal mistakes is to help keep human family sizes small. Smaller families could allow parents to focus more attention and resources on offspring, increasing survival.


Found in: Body & Brain and Humans
Comments 6
  • Perhaps the female half of the chomasome material is supposed to more closely resemble the "host" of the embryo in order that the body doesn't reject the embryo. Could that be why mitochondrial DNA in the baby is always identical to the mother's mitochondrial DNA?
    luv2teach luv2teach
    Nov. 12, 2008 at 8:45pm
  • We actually know one reason for recombination -- it provides greater diversity. Diversity, in turn, provides the raw material which enables evolution to adapt species to changes in the environment. Many mutations are indeed errors, but seem to improvements and are thus passed along to future generations. We also know that some errors, such as the one that causes Down's syndrome, are more likely to occur when the eggs (and the mother) are older. In very ancient times, few women lived long enough to continue giving birth into their 50s. So it didn't matter that the process wasn't very tidy at that point. We evolved to have our last child around 35, I imagine, which is when the process begins not to work so well. Jane Goodall noted that older chimpanzee mothers sometimes died when their last baby was not yet old enough to fend for itself, too (1986), with tragic results for that last infant, even if that last offspring was normal. So in "olden times" these sorts of things tended to work themselves out in a very rough and tumble fashion.
    Diana Gainer Diana Gainer
    Nov. 13, 2008 at 10:38am
  • If, as stated, fathers NEVER pass along any chromosome abnormality, how is an XYY or XY(n) male created, then? Surely this chromosome abnormality cannot be the result of nondisjunction in the mother's oogonia, considering there are only X's there. In these cases, it MUST be the father who is passing on the problematic Y's. And if the father is passing on two Y's in one gamete, surely they may also be the reason for some Turner females lacking a second sex chromosome? Perhaps the sperm lacking the sex chromosome was the sister cell to the double Y sperm.
    k g k g
    Nov. 15, 2008 at 8:58pm
  • women frequently died in child birth.
    families were large and aunts and uncles took over raising the dead mother's children unless the older siblings did this for their brothers. Girls frequently had sexual relations with men who looked after them. Back in our old times, children as well as women were property and in case of debt they were used for payment of these debts. Becoming children in a richer family was often an advantage for them.
    Heinz  Gf. Matuschka Heinz Gf. Matuschka
    Nov. 16, 2008 at 10:11pm
  • Organism Replication Is Its Accelerated Re-Genesis-Evolution
    Roots Of Sex And Replication


    A. Women's chromosome division different from men's
    http://www.sciencenews.org/view/generic/id/38528/title/Womens_chromosome_division_different_from_mens
    Using fluorescent markers, scientists are discovering that men and women divide chromosomes differently.


    B. Replication of organisms, in

    http://www.biology.arizona.edu/Cell_BIO/tutorials/pev/main.html

    a. RNA Viruses: reproduce in host cells, no growth on artificial media, no division by binary fission, no protein synthesis machinery, not sensitive to antibiotics.

    b. Binary fission: the process in which a parent cell splits into two daughter cells of approximately equal size. Simple cell division in single-celled organisms.

    c. Prokaryotes: DNA chromosomal ring, plasmid extrachromosomal ring autonomous replication, the
    plasmids are self-replicating circular molecules of DNA in many bacterial, archaeal, fungal, algal, and plant species.


    C. Sex in prokaryotes, bacteria

    http://www.biology.arizona.edu/Cell_BIO/tutorials/pev/page2.html

    In prokaryotes, bacteria, you can have sex, with males possessing a sexual apparatus for transferring 'genetic information' to receptive females. However, since you are both always going 30 mph it is difficult to find each other. Furthermore, if you are male, nature gave you a severe problem. Every time you mate with a female, she turns into a male. In bacteria, "maleness" is an infective venereal disease. Also, at fairly high frequencies, spontaneous mutations cause you to turn into a female.

    Some bacteria have sex pili which are responsible for bacteria recognizing one another and the consequent formation of a conjugation tube which allows the transfer of DNA from a "male" cell to a "female" cell. In this way, recombination occurs and the resulting cell will contain a combination of genes from each parent cell. 'Male' and 'female' are donnor and receiver.


    D. Sex: process of recombining genes to form new and unique combinations

    - Every organism's replication is an accelerated re-run of its genesis-plus-evolution.

    - Male-female divisions and relationships and all sex forms are evolutionary developments of prokaryotes' sex, driven by the need to recombine the genes held in the double-helixed DNA, in order to maintain life on Earth (... within the human body about 3 billion cells die every minute...).

    Suggesting,

    Dov Henis

    (A DH Comment From The 22nd Century)
    http://blog.360.yahoo.com/blog-P81pQcU1dLBbHgtjQjxG_Q--?cq=1

    Dov Henis Dov Henis
    Nov. 18, 2008 at 10:04pm
  • Recurrent spontaneous abortion (RSA), which is defined as two or more consecutive pregnancy losses before 22 weeks of gestation, is a prevalent disorder. It has been estimated to occur in 1-2% of couples wishing to have children. Although known causes of RSA include anatomic (15%), infectious (1-2%), hormonal (20%), immunologic (20%), and genetic (2-5%) disorders, 37-79% of those couples will not receive an explanation for their pregnancy losses. Recently, the finding was reported that skewed X chromosome inactivation was increased in women with RSA. X chromosome inactivation is defined as one of the two X chromosomes in each somatic cell of healthy human females becomes inactivated very early in embryonic development. This inactivation occurs randomly, on both the maternal and paternal X chromosome. Several studies have suggested that X-linked mutations underlie between RSA and skewed X chromosome inactivation. This hypothesis proposes that male lethal X-linked mutations cause skewed inactivation in female carriers. Many X-linked syndromes have been described in which carrier females exhibit highly skewed X inactivation. Such mutations are lethal to hemizygous male offsprings who inherit them, resulting in increased frequencies of spontaneous abortion in carrier females. To investigate whether skewed X chromosome inactivation is the potential cause of RSA or not, we studied DNA methylation patterns of the X-linked AR gene in patients experienced at least two losses as compared with reproductive women. To read more about this article, check out at: http://personalmoneystore.com/moneyblog/2009/03/19/payday-loans-money-urgently/
    Mya D Mya D
    Mar. 27, 2009 at 12:01am
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