{Reference Type}: Journal Article
{Title}: Molecular characterization of the Yp11.2 region deletion in the Chinese Han population.
{Author}: Pang Q;Lin Q;Wang D;Sun Z;Wang J;
{Journal}: Int J Legal Med
{Volume}: 135
{Issue}: 4
{Year}: Jul 2021
{Factor}: 2.791
{DOI}: 10.1007/s00414-021-02596-x
{Abstract}: The Y chromosome is male-specific and is important for spermatogenesis and male fertility. However, the Y chromosome is poorly characterized due to massive palindromes and inverted repeats, which increase the likelihood of genomic rearrangements, resulting in short tandem repeats on the Y chromosome or long fragment deletions. The present study reports a large-scale (2.573~2.648 Mb) deletion in the Yp11.2 region in a Chinese population based on the analysis of 34 selected Y-specific sequence-tagged sites and subsequent sequencing of the breakpoint junctions on the Y chromosome from 5,068,482-5,142,391 bp to 7,715,462-7,716,695 bp. The results of sequence analysis indicated that the deleted region included part or all of the following five genes: PCDH11Y, TSPY, AMELY, TBL1Y, and RKY. These genes are associated with spermatogenesis or amelogenesis and various other processes; however, specific physiological functions and molecular mechanisms of these genes remain unclear. Notably, individuals with this deletion pattern did not have an obvious pathological phenotype but manifested some degree of amelogenesis imperfecta.