AI Article Synopsis

  • The proterminal region of human chromosome 3p is unusually GC-poor and gene-poor compared to other chromosomes, which may contribute to certain fatal diseases due to potential loss of heterozygosity.
  • Sequencing revealed this region has a GC content of 38.5%, the lowest among human proterminal regions, and contains 20 known and 22 predicted genes with a large average gene size of 97.5 kb.
  • Furthermore, interspersed repeats in this region are highly active, particularly (TA)n repeats, and a conserved synteny exists with a section of mouse chromosome 6, implying significant differences in nucleotide retention and repeat activity relative to the whole genome.

Article Abstract

Most proterminal regions of human chromosomes are GC-rich and gene-rich. Chromosome 3p is an exception. Its proterminal region is GC-poor, and likely to lose heterozygosity, thus causing a number of fatal diseases. Except one gap left in the telomeric position, the proterminal region of human chromosome 3p has been completely sequenced. The detailed sequence analysis showed: (i) the GC content of this region was 38.5%, being the lowest among all the human proterminal regions; (ii) this region contained 20 known genes and 22 predicted genes, with an average gene size of 97.5 kb. The previously mapped gene Cntn3 was not found in this region, but instead located in the 74 Mb position of human chromosome 3p; (iii) the interspersed repeats of this region were more active than the average level of the whole human genome, especially (TA)n, the content of which was twice the genome average; (iv) this region had a conserved synteny extending from 104.1 Mb to 112.4 Mb on the mouse chromosome 6, which was 8% larger in size, not in accordance with the whole genome comparison, probably because the 3pter-p26 region was more likely to lose nucleotides and its mouse synteny had more active interspersed repeats.

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http://dx.doi.org/10.1360/03yc0131DOI Listing

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