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X-CHROMOSOME INACTIVATION:
MOLECULAR MECHANISM AND
GENETIC CONSEQUENCES




               By: Ambaye, S. & Mujahed, H
INTODUCTION

   What makes a child a boy or a girl ?

   X-Chromosome and Y-chromosome
    are different.

   Males and Females should
    have the same amount
    X-chromsome genes
    product.
INTODUCTION

   Dosage Compensation
    A mechanism to equalize the dosage of X-
    chromosome gene products by means of
    inactivating one of female X-chromosomes in
    mammels.

   In Drosophila dosage Compensation
    accompleished by two fold transcriptional
    upregulation male X chromosome.
   The existence of XCI was first suggested by Mary
    Lyon in 1961.

   For this reason this suggestion was known as the
    `Lyon hypothesis,'
MOLECULAR MECHANISMS OF X INACTIVATION

   X-chromosome contains X Inactivation Center (XIC)
    which located in long arm.

   XIC contains an unusual gene called inactive X
    (Xi)-specific transcripts (XIST).

   XIST expresses a noncoding functional 17 (kb)
    RNA molecule.

   XIST expressed only when more than one X-
    chromosome found in same cell.
MOLECULAR MECHANISMS OF X INACTIVATION




                                   (Migeon, 1994)
MOLECULAR MECHANISMS OF X INACTIVATION

          XIST




                               (Brown, C. J. et al. 1991)
MOLECULAR MECHANISMS OF X INACTIVATION

   XIST transcripts remains in the nucleus.

   While Xist is being transcribed, blocking factors
    prevent the association with X chromosome.
MOLECULAR MECHANISMS OF X INACTIVATION

   Blocking factores are released, Xist RNA is
    stablized and upregulated.
MOLECULAR MECHANISMS OF X INACTIVATION

   Before inactivation the X chromosome coated with
    stabilized Xist RNA.
MOLECULAR MECHANISMS OF X INACTIVATION

   Genes on the X chromosome are silenced following
    Xist RNA coating using an unknown mechanism.
MOLECULAR MECHANISMS OF X INACTIVATION

    Chromatin modifications, including histone
    deacetylation and methylation of promoters of X-
    linked.




                                        (Avner, P., & Heard, 2001)
GENETIC IMPRINTING AND X INACTIVATION

   X-chromosome inactivation ocurres by two ways:
    Random and imprented.

Differes in:
     Developmental timing.
     Mechanism.
GENETIC IMPRINTING

    Paternal X-chromosome is preferentially silenced
    in the placenta.

   Extensive methylation of CpG islands on paternal
    X-chromosome.

   Suggested to take a place during spermatogenesis.
GENETIC IMPRINTING

       Summary of
       Fthl17 gene
          family
      expression in
     preimplantation
     stage embryos.




                Kobayashi S et al. Nucl. Acids Res. 2010;nar.gkq113
© The Author(s) 2010. Published by Oxford University Press.
RANDOM X INACTIVATION

   One of the two X-chromosomes is randomly
    inactivated in the early female embryo
    developmental stage.

   Cells ensure that one
    of the Xs still active.
RANDOM X INACTIVATION
CONSEQUENCES OF X CHROMOSOME
INACTIVATION

   The result is that the effective dosages of products
    of X-linked genes are equal in males and females.

   The X chromosome is large and with many genes,
    whereas the Y chromosome
    is much smaller and carries
     orthologs of only a few of the
     X-linked genes.
CONSEQUENCES OF X CHROMOSOME
INACTIVATION

   Inactivation in females results in cellular mosaicsim,
    one population of cells expresses the maternal
    allele; the other expresses the paternal one.
CONSEQUENCES OF X CHROMOSOME
INACTIVATION

   Females benefit from the presence of heterozygous
    populations of cells.

   In case of X-linked mutations that are detrimental
    and even lethal, sons may not be affected of the
    mutant gene they express.

   Also growth competition between the mosaic
    populations can result in elimination of cells that
    express the mutant allele.
CONSEQUENCES OF X CHROMOSOME
INACTIVATION

   X inactivation can create problems when cells with
    the mutation have a growth advantage (e.g: cancer
    cells).

   Elimination of normal cells occurs as the result of
    chromosomal abnormalities that arise by chance.

   As a consequence, females may manifest diseases
    usually found only in males
“It has been six weeks now. Six weeks of tireless,
  frenzied activity since that sperm jostled its way
  into that egg. So little time spent in this warm,
  dark, womby home, and so much achieved”


                             David Bainbridge, The X In Sex
REFERENSES

Avner, P. and Heard, E. (2001). X-chromosome inactivation: counting, choice
  and initiation. Nat Rev Genet 2, 59-67.
Brown, C. J., Ballabio, A., Rupert, J. L., Lafreniere, R. G., Grompe, M.,
  Tonlorenzi, R. and Willard, H. F. (1991). A gene from the region of the
  human X inactivation centre is expressed exclusively from the inactive X
  chromosome. Nature 349, 38-44.
Migeon, B. R. (1994). X-chromosome inactivation: molecular mechanisms and
  genetic consequences. Trends Genet 10, 230-235.
Yang, C., Chapman, A. G., Kelsey, A. D., Minks, J., Cotton, A. M. and Brown,
  C. J. (2011). X-chromosome inactivation: molecular mechanisms from the
  human perspective. Hum Genet.

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X chromosome inactivation ambaye, s. & mujahed, h.

  • 1. X-CHROMOSOME INACTIVATION: MOLECULAR MECHANISM AND GENETIC CONSEQUENCES By: Ambaye, S. & Mujahed, H
  • 2. INTODUCTION  What makes a child a boy or a girl ?  X-Chromosome and Y-chromosome are different.  Males and Females should have the same amount X-chromsome genes product.
  • 3. INTODUCTION  Dosage Compensation A mechanism to equalize the dosage of X- chromosome gene products by means of inactivating one of female X-chromosomes in mammels.  In Drosophila dosage Compensation accompleished by two fold transcriptional upregulation male X chromosome.
  • 4. The existence of XCI was first suggested by Mary Lyon in 1961.  For this reason this suggestion was known as the `Lyon hypothesis,'
  • 5. MOLECULAR MECHANISMS OF X INACTIVATION  X-chromosome contains X Inactivation Center (XIC) which located in long arm.  XIC contains an unusual gene called inactive X (Xi)-specific transcripts (XIST).  XIST expresses a noncoding functional 17 (kb) RNA molecule.  XIST expressed only when more than one X- chromosome found in same cell.
  • 6. MOLECULAR MECHANISMS OF X INACTIVATION (Migeon, 1994)
  • 7. MOLECULAR MECHANISMS OF X INACTIVATION XIST (Brown, C. J. et al. 1991)
  • 8. MOLECULAR MECHANISMS OF X INACTIVATION  XIST transcripts remains in the nucleus.  While Xist is being transcribed, blocking factors prevent the association with X chromosome.
  • 9. MOLECULAR MECHANISMS OF X INACTIVATION  Blocking factores are released, Xist RNA is stablized and upregulated.
  • 10. MOLECULAR MECHANISMS OF X INACTIVATION  Before inactivation the X chromosome coated with stabilized Xist RNA.
  • 11. MOLECULAR MECHANISMS OF X INACTIVATION  Genes on the X chromosome are silenced following Xist RNA coating using an unknown mechanism.
  • 12. MOLECULAR MECHANISMS OF X INACTIVATION  Chromatin modifications, including histone deacetylation and methylation of promoters of X- linked. (Avner, P., & Heard, 2001)
  • 13. GENETIC IMPRINTING AND X INACTIVATION  X-chromosome inactivation ocurres by two ways: Random and imprented. Differes in:  Developmental timing.  Mechanism.
  • 14. GENETIC IMPRINTING  Paternal X-chromosome is preferentially silenced in the placenta.  Extensive methylation of CpG islands on paternal X-chromosome.  Suggested to take a place during spermatogenesis.
  • 15. GENETIC IMPRINTING Summary of Fthl17 gene family expression in preimplantation stage embryos. Kobayashi S et al. Nucl. Acids Res. 2010;nar.gkq113 © The Author(s) 2010. Published by Oxford University Press.
  • 16. RANDOM X INACTIVATION  One of the two X-chromosomes is randomly inactivated in the early female embryo developmental stage.  Cells ensure that one of the Xs still active.
  • 18. CONSEQUENCES OF X CHROMOSOME INACTIVATION  The result is that the effective dosages of products of X-linked genes are equal in males and females.  The X chromosome is large and with many genes, whereas the Y chromosome is much smaller and carries orthologs of only a few of the X-linked genes.
  • 19. CONSEQUENCES OF X CHROMOSOME INACTIVATION  Inactivation in females results in cellular mosaicsim, one population of cells expresses the maternal allele; the other expresses the paternal one.
  • 20. CONSEQUENCES OF X CHROMOSOME INACTIVATION  Females benefit from the presence of heterozygous populations of cells.  In case of X-linked mutations that are detrimental and even lethal, sons may not be affected of the mutant gene they express.  Also growth competition between the mosaic populations can result in elimination of cells that express the mutant allele.
  • 21. CONSEQUENCES OF X CHROMOSOME INACTIVATION  X inactivation can create problems when cells with the mutation have a growth advantage (e.g: cancer cells).  Elimination of normal cells occurs as the result of chromosomal abnormalities that arise by chance.  As a consequence, females may manifest diseases usually found only in males
  • 22. “It has been six weeks now. Six weeks of tireless, frenzied activity since that sperm jostled its way into that egg. So little time spent in this warm, dark, womby home, and so much achieved” David Bainbridge, The X In Sex
  • 23. REFERENSES Avner, P. and Heard, E. (2001). X-chromosome inactivation: counting, choice and initiation. Nat Rev Genet 2, 59-67. Brown, C. J., Ballabio, A., Rupert, J. L., Lafreniere, R. G., Grompe, M., Tonlorenzi, R. and Willard, H. F. (1991). A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome. Nature 349, 38-44. Migeon, B. R. (1994). X-chromosome inactivation: molecular mechanisms and genetic consequences. Trends Genet 10, 230-235. Yang, C., Chapman, A. G., Kelsey, A. D., Minks, J., Cotton, A. M. and Brown, C. J. (2011). X-chromosome inactivation: molecular mechanisms from the human perspective. Hum Genet.