Genes on the X chromosome, which regulate embryonic development, are the focus of the current publication in the journal Genome Research. Men have only one X chromosome, and therefore mutations on this chromosome disproportionately affect males, frequently leading to serious diseases such as hemophilia, muscular dystrophy and mental retardation.
Scientists of Helmholtz Zentrum München led by Dr. Heiko Lickert, principal investigator at the Institute of Stem Cell Research, in cooperation with the group led by Professor Janet Rossant at the Hospital for Sick Children in Toronto, investigated which X-linked genes are relevant to disease. They reported their findings in Genome Research, a leading journal on human genetics.
In cooperation with the Gene Trap Consortium coordinated by Professor Wolfgang Wurst of the Institute of Developmental Genetics, 58 genes were tested. That corresponds to 10 percent of the syntenic* genes on the X chromosome. 17 of these 58 genes are essential for embryonic development and for 9 of these genes, mouse models for human diseases were generated. These models will be studied in detail in follow-up studies in order to gain new insights about the causes of human diseases.
For the first time, the effect of the respective mutation on embryonic development could be shown without generating individual mouse models. Until now, mutation screens were essential to close such knowledge gaps, but such screens are associated with much effort and expense. "This study brings us much closer to our goal of understanding the genetic causes of all X-linked diseases," Dr. Lickert said.
Background
Except for the sex chromosomes, the chromosomes in the human genome occur in pairs. While women have two X chromosomes, men have only one X chromosome and one considerably smaller Y chromosome. That is why for a multitude of genes, men do not have a second copy which could inactivate mutations. In men, X-linked mutations lead to an above-average number of diseases.
* Synteny: Commonalities in the sequence of genes or gene fragments on different chromosome segments when comparing different species (here human and mouse).
Scientists of Helmholtz Zentrum München led by Dr. Heiko Lickert, principal investigator at the Institute of Stem Cell Research, in cooperation with the group led by Professor Janet Rossant at the Hospital for Sick Children in Toronto, investigated which X-linked genes are relevant to disease. They reported their findings in Genome Research, a leading journal on human genetics.
In cooperation with the Gene Trap Consortium coordinated by Professor Wolfgang Wurst of the Institute of Developmental Genetics, 58 genes were tested. That corresponds to 10 percent of the syntenic* genes on the X chromosome. 17 of these 58 genes are essential for embryonic development and for 9 of these genes, mouse models for human diseases were generated. These models will be studied in detail in follow-up studies in order to gain new insights about the causes of human diseases.
For the first time, the effect of the respective mutation on embryonic development could be shown without generating individual mouse models. Until now, mutation screens were essential to close such knowledge gaps, but such screens are associated with much effort and expense. "This study brings us much closer to our goal of understanding the genetic causes of all X-linked diseases," Dr. Lickert said.
Background
Except for the sex chromosomes, the chromosomes in the human genome occur in pairs. While women have two X chromosomes, men have only one X chromosome and one considerably smaller Y chromosome. That is why for a multitude of genes, men do not have a second copy which could inactivate mutations. In men, X-linked mutations lead to an above-average number of diseases.
* Synteny: Commonalities in the sequence of genes or gene fragments on different chromosome segments when comparing different species (here human and mouse).
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