Abstract
It is widely accepted that only one of two X chromosomes present in the somatic cells of female mammals is active (Lyon 1961). This results in a similar dosage relationship between functional X chromosomes and autosomes in females and males. This compensation occurs early in development between the 2-cell stage (Hoppe and Whitten 1972) and the time of implantation of the embryo into the uterus (Gardner and Lyon 1971). An important issue concerning X-chromosome differentiation is the functional state of X chromosomes during early embryogenesis, before irreversible dosage compensation occurs. That is, does X-chromosome differentiation involve a process of X-chromosome inactivation or X-chromosome activation? Choosing between these alternatives is important for understanding a number of features of X-chromosome differentiation, including:
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(1)
the derivation of molecular and genetic models of this process, and
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(2)
the determination of the timing of this differentiation.
In the latter instance, activation and inactivation events may pose entirely different conditions for using biochemical variants of X-linked genes for studying the developmental timing of the event.
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References
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Chapman, V.M., West, J.D., Adler, D.A. (1978). Bimodal Distribution of α-Galactosidase Activities in Mouse Embryos. In: Russell, L.B. (eds) Genetic Mosaics and Chimeras in Mammals. Basic Life Sciences, vol 12. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-3390-6_17
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DOI: https://doi.org/10.1007/978-1-4684-3390-6_17
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