Komaki Haruna, Oi Maya, Suzuki Hiroshi
Research Unit for Functional Genomics, National Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Inada, Obihiro, Japan.
Research Unit for Functional Genomics, National Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Inada, Obihiro, Japan; Department of Basic Veterinary Science, The United Graduate School of Veterinary Sciences, Gifu University, Gifu, Japan.
Theriogenology. 2014 Sep 1;82(4):652-6. doi: 10.1016/j.theriogenology.2014.05.018. Epub 2014 May 27.
With the development of a direct visualization of sex chromosome in a single sperm by fluorescence in situ hybridization (FISH) technique, the frequency of aberration (aneuploidy) in spermatozoa in several mammals has been investigated. However, there is no report in the incidence of X-Y aneuploidy in the sperm population of dogs. Therefore, in this study, the aneuploidy in dog spermatozoa was examined by multicolor FISH using specific molecular probes for canine sex chromosomes and autosome. Semen from eight male Labrador retrievers was used as specimen. For decondensation of sperm nuclei, the specimen was treated with 1 M NaOH for 4 minutes at room temperature. Probes for chromosomes X, Y, and 1, labeled with SpectrumGreen, Cy3 and Cy5, respectively, were hybridized with decondensed spermatozoa. Fluorescence in situ hybridization signals in sperm heads were clearly detected in each specimen, regardless of the sperm donor. The FISH signal of at least one of the three probes was detected in all sperm heads examined. There was no significant difference between the theoretical ratio (50:50) and the observed ratio of X and Y chromosomes in spermatozoa of all the eight dogs. Mean percentage of sex chromosome aneuploidy was 0.127% (ranged between 0% and 0.316%). This percentage of canine sex chromosome aneuploidy was lower than the one reported in cattle, horses, river buffalo, and goats sperm, but higher than that observed in mice and sheep.
随着荧光原位杂交(FISH)技术在单个精子中对性染色体进行直接可视化的发展,已对几种哺乳动物精子中的畸变(非整倍体)频率进行了研究。然而,关于犬精子群体中X-Y非整倍体发生率尚无报道。因此,在本研究中,使用针对犬性染色体和常染色体的特异性分子探针,通过多色FISH检测犬精子中的非整倍体。以8只雄性拉布拉多猎犬的精液作为样本。为使精子核去浓缩,样本在室温下用1 M NaOH处理4分钟。分别用SpectrumGreen、Cy3和Cy5标记的X、Y和1号染色体探针与去浓缩的精子进行杂交。在每个样本中均能清晰检测到精子头部的荧光原位杂交信号,与精子供体无关。在所检测的所有精子头部均检测到三种探针中至少一种的FISH信号。在所有8只犬的精子中,X和Y染色体的理论比例(50:50)与观察比例之间无显著差异。性染色体非整倍体的平均百分比为0.127%(范围在0%至0.316%之间)。犬性染色体非整倍体的这一百分比低于牛、马、河水牛和山羊精子中报道的比例,但高于小鼠和绵羊中观察到的比例。