Bérubé M, Palsbøll P
Department of Population Biology, University of Copenhagen, Denmark,
Mol Ecol. 1996 Apr;5(2):283-7. doi: 10.1111/j.1365-294x.1996.tb00315.x.
We sequenced 540 nucleotides of the last exon in the ZFY/ZFX gene in two males and two females for eight cetacean species; four odontocetes (toothed whales) and four mysticetes (baleen whales). Based upon the obtained nucleotide sequences, we designed two sets of oligonucleotide primers for specific amplification of the ZFX and the ZFY sequence in odontocetes and mysticetes, respectively. Each primer set consisted of three oligonucleotides; one forward-orientated primer, which anneals to the ZFY as well as the ZFX sequence, and two reverse-orientated primers that anneal to either the ZFX or or the ZFY sequence. The resulting two amplification products (specific for the ZFY and ZFX sequences) can be distinguished by gel-electrophoresis through 2% NuSieve(TM). The accuracy of the technique was tested by determination of gender in 214 individuals of known sex. Finally we applied the technique to determine the sex of 3570 cetacean specimens; 2284 humpback whales, 315 fin whales, 37 blue whales, 7 minke whales, as well as 592 belugas, 335 narwhals and 25 harbour porpoises.
我们对8种鲸类动物(4种齿鲸和4种须鲸)的2只雄性和2只雌性个体的ZFY/ZFX基因最后一个外显子的540个核苷酸进行了测序。根据获得的核苷酸序列,我们分别设计了两组寡核苷酸引物,用于特异性扩增齿鲸和须鲸中的ZFX和ZFY序列。每组引物由三个寡核苷酸组成;一个正向引物,它可与ZFY以及ZFX序列退火,还有两个反向引物,它们分别与ZFX或ZFY序列退火。通过2% NuSieve(TM)凝胶电泳可以区分产生的两种扩增产物(分别针对ZFY和ZFX序列)。通过确定214个已知性别的个体的性别来测试该技术的准确性。最后,我们应用该技术来确定3570个鲸类标本的性别;其中包括2284头座头鲸、315头长须鲸、37头蓝鲸、7头小须鲸,以及592头白鲸、335头独角鲸和25头港湾鼠海豚。