de Pauw E S D, Roelofs H, Zwinderman A, van Houwelingen J C, Fibbe W E, de Knijff P, Pearson P L, Tanke H J
Department of Haematology, Leiden University Medical Center, Leiden, The Netherlands.
Cytometry A. 2005 May;65(1):35-9. doi: 10.1002/cyto.a.20131.
Consistent average length differences between species and chromosome arm differences within species indicate that telomere length is genetically determined. This seems to contradict an observed large variation in lengths of the same human telomere between metaphases of the same individual. We examined the extent to which the variation in the telomeres of the human X and Y chromosomes is heritable, induced, or technical in origin.
Metaphase chromosomes were stained by fluorescence in situ hybridization with a telomere repeat-specific probe, and fluorescence intensities of the X and Y chromosomes were measured. If telomere length variation is predominantly genetically determined and a 50% probability of meiotic recombination between the pseudo-autosomal regions of Yp and Xp in the father is taken into account, one expects an equal chance that the Yp telomere of a son is derived from his father's Xp or Yp telomere. This implies that the Yp/Yq telomere ratios in fathers and sons will be identical in the absence of paternal meiotic recombination and different when recombination occurs.
Among five father-son pairs, four showed similar Yp/Yq ratios (P > 0.05), whereas one pair exhibited a large difference in the Yp/Yq ratio that was attributable to a significantly longer Xp than Yp telomere in the father and a presumptive meiotic exchange between X and Y during paternal meiosis. Further, the Xq telomere exhibited a generally shorter telomere length than the others.
The high variation in telomere length appeared to be intracellular (between sister chromatids) and, hence, technical in nature. We found no measurable induced variation in the cells studied, implying that, if induced variation exists, it is small compared with the technical variation.
物种间一致的平均长度差异以及物种内染色体臂差异表明端粒长度是由基因决定的。这似乎与在同一个体的中期相中观察到的相同人类端粒长度存在巨大差异相矛盾。我们研究了人类X和Y染色体端粒变异在多大程度上是可遗传的、诱导产生的或技术原因导致的。
用端粒重复序列特异性探针通过荧光原位杂交对中期染色体进行染色,并测量X和Y染色体的荧光强度。如果端粒长度变异主要由基因决定,并且考虑到父亲Yp和Xp的假常染色体区域之间减数分裂重组的概率为50%,那么可以预期儿子的Yp端粒来自其父亲的Xp或Yp端粒的机会均等。这意味着在没有父本减数分裂重组的情况下,父子的Yp/Yq端粒比率将相同,而当发生重组时则不同。
在五对父子中,四对的Yp/Yq比率相似(P>0.05),而有一对的Yp/Yq比率差异很大,这是由于父亲的Xp端粒比Yp端粒长得多,并且在父本减数分裂期间X和Y之间可能发生了减数分裂交换。此外,Xq端粒的长度通常比其他端粒短。
端粒长度的高度变异似乎是细胞内的(姐妹染色单体之间),因此本质上是技术原因导致的。我们在所研究的细胞中未发现可测量的诱导变异,这意味着如果存在诱导变异,与技术变异相比它很小。