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The DNA sequence of the human X chromosome.

Nature (2005-03-18)
Mark T Ross, Darren V Grafham, Alison J Coffey, Steven Scherer, Kirsten McLay, Donna Muzny, Matthias Platzer, Gareth R Howell, Christine Burrows, Christine P Bird, Adam Frankish, Frances L Lovell, Kevin L Howe, Jennifer L Ashurst, Robert S Fulton, Ralf Sudbrak, Gaiping Wen, Matthew C Jones, Matthew E Hurles, T Daniel Andrews, Carol E Scott, Stephen Searle, Juliane Ramser, Adam Whittaker, Rebecca Deadman, Nigel P Carter, Sarah E Hunt, Rui Chen, Andrew Cree, Preethi Gunaratne, Paul Havlak, Anne Hodgson, Michael L Metzker, Stephen Richards, Graham Scott, David Steffen, Erica Sodergren, David A Wheeler, Kim C Worley, Rachael Ainscough, Kerrie D Ambrose, M Ali Ansari-Lari, Swaroop Aradhya, Robert I S Ashwell, Anne K Babbage, Claire L Bagguley, Andrea Ballabio, Ruby Banerjee, Gary E Barker, Karen F Barlow, Ian P Barrett, Karen N Bates, David M Beare, Helen Beasley, Oliver Beasley, Alfred Beck, Graeme Bethel, Karin Blechschmidt, Nicola Brady, Sarah Bray-Allen, Anne M Bridgeman, Andrew J Brown, Mary J Brown, David Bonnin, Elspeth A Bruford, Christian Buhay, Paula Burch, Deborah Burford, Joanne Burgess, Wayne Burrill, John Burton, Jackie M Bye, Carol Carder, Laura Carrel, Joseph Chako, Joanne C Chapman, Dean Chavez, Ellson Chen, Guan Chen, Yuan Chen, Zhijian Chen, Craig Chinault, Alfredo Ciccodicola, Sue Y Clark, Graham Clarke, Chris M Clee, Sheila Clegg, Kerstin Clerc-Blankenburg, Karen Clifford, Vicky Cobley, Charlotte G Cole, Jen S Conquer, Nicole Corby, Richard E Connor, Robert David, Joy Davies, Clay Davis, John Davis, Oliver Delgado, Denise Deshazo
RESUMEN

The human X chromosome has a unique biology that was shaped by its evolution as the sex chromosome shared by males and females. We have determined 99.3% of the euchromatic sequence of the X chromosome. Our analysis illustrates the autosomal origin of the mammalian sex chromosomes, the stepwise process that led to the progressive loss of recombination between X and Y, and the extent of subsequent degradation of the Y chromosome. LINE1 repeat elements cover one-third of the X chromosome, with a distribution that is consistent with their proposed role as way stations in the process of X-chromosome inactivation. We found 1,098 genes in the sequence, of which 99 encode proteins expressed in testis and in various tumour types. A disproportionately high number of mendelian diseases are documented for the X chromosome. Of this number, 168 have been explained by mutations in 113 X-linked genes, which in many cases were characterized with the aid of the DNA sequence.

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