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The DNA sequence and comparative analysis of human chromosome 5
Authors:Schmutz Jeremy  Martin Joel  Terry Astrid  Couronne Olivier  Grimwood Jane  Lowry Steve  Gordon Laurie A  Scott Duncan  Xie Gary  Huang Wayne  Hellsten Uffe  Tran-Gyamfi Mary  She Xinwei  Prabhakar Shyam  Aerts Andrea  Altherr Michael  Bajorek Eva  Black Stacey  Branscomb Elbert  Caoile Chenier  Challacombe Jean F  Chan Yee Man  Denys Mirian  Detter John C  Escobar Julio  Flowers Dave  Fotopulos Dea  Glavina Tijana  Gomez Maria  Gonzales Eidelyn  Goodstein David  Grigoriev Igor  Groza Matthew  Hammon Nancy  Hawkins Trevor  Haydu Lauren  Israni Sanjay  Jett Jamie  Kadner Kristen  Kimball Heather  Kobayashi Arthur  Lopez Frederick
Affiliation:Stanford Human Genome Center, Department of Genetics, Stanford University School of Medicine, 975 California Ave, Palo Alto, California 94304, USA. jeremy@shgc.stanford.edu
Abstract:
Chromosome 5 is one of the largest human chromosomes and contains numerous intrachromosomal duplications, yet it has one of the lowest gene densities. This is partially explained by numerous gene-poor regions that display a remarkable degree of noncoding conservation with non-mammalian vertebrates, suggesting that they are functionally constrained. In total, we compiled 177.7 million base pairs of highly accurate finished sequence containing 923 manually curated protein-coding genes including the protocadherin and interleukin gene families. We also completely sequenced versions of the large chromosome-5-specific internal duplications. These duplications are very recent evolutionary events and probably have a mechanistic role in human physiological variation, as deletions in these regions are the cause of debilitating disorders including spinal muscular atrophy.
Keywords:
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