US Environmental Protection Agency, Office of Research and Development, National Health and Environmental Effects Research Laboratory, Mid-Continent Ecology Division, 6201 Congdon Blvd, Duluth, MN, United States.
Aquat Toxicol. 2010 Jun 1;98(1):60-6. doi: 10.1016/j.aquatox.2010.01.012. Epub 2010 Jan 25.
Endocrine disrupting compounds have been shown to alter gonad differentiation in both male and female individuals in amphibian, avian, fish, invertebrate, and reptile species. In some cases, these affected individuals are completely sex reversed and are morphologically indistinguishable from normal individuals of the opposite sex. Detecting shifts in sex ratios following chemical exposure often requires large numbers of organisms to achieve the necessary statistical power, especially in those species with genetic sex determination and homomorphic sex chromosomes (such as amphibians and many fish). The ability to assess the genetic sex of individuals would allow for detection of sex reversal (genotype-phenotype mismatches) that have greater statistical power compared to examining changes in sex ratios. Utilizing amplified fragment length polymorphisms (AFLPs), we developed a method for genotyping sex in the amphibian, Xenopus (Silurana) tropicalis, that can be incorporated into endocrine disruptor screening assays that examine the effects of chemicals on gonad differentiation. AFLPs from 512 primer pairs were assessed in one spawn of X. tropicalis. Each primer pair yielded, on average, 100 fragments. In total 17 sex-linked AFLPs were identified, isolated, and sequenced. A recombination map of these AFLPs was generated using over 300 individuals with four AFLPs having a recombination rate of 0% with regard to sex. A BLASTn search of the X. tropicalis genome using these AFLP sequences resulted in identification of sex-linked scaffolds. Areas of these scaffolds were searched for additional polymorphisms that could be utilized for genotyping sex. Retrospective and prospective strategies for incorporating genotyping sex in endocrine disruptor bioassays with X. tropicalis were developed. A Monte Carlo simulation comparing analyzing data as sex ratio shifts versus assessment of sex reversal using genotyping demonstrates the increase in statistical power that can be obtained by genotyping sex in studies dealing with altered gonad differentiation. This approach to identifying sex-linked markers and developing sex genotyping methods is applicable to other species with genetic sex determination.
内分泌干扰化合物已被证明会改变两栖动物、鸟类、鱼类、无脊椎动物和爬行动物的雌雄个体的性腺分化。在某些情况下,这些受影响的个体完全发生了性反转,在形态上与异性的正常个体无法区分。在化学暴露后检测性别比例的变化通常需要大量的生物来获得必要的统计能力,特别是在那些具有遗传性别决定和同形性染色体的物种中(如两栖动物和许多鱼类)。评估个体遗传性别的能力将能够检测到性反转(基因型-表型不匹配),与检查性别比例变化相比,这具有更大的统计能力。我们利用扩增片段长度多态性(AFLP)技术,开发了一种在两栖动物 Xenopus (Silurana) tropicalis 中进行基因分型的方法,该方法可用于内分泌干扰物筛选试验中,以检查化学物质对性腺分化的影响。在 X. tropicalis 的一次产卵中评估了 512 对引物的 AFLP。每个引物平均产生 100 个片段。总共鉴定、分离和测序了 17 个与性别相关的 AFLP。使用超过 300 个个体生成了这些 AFLP 的重组图谱,其中 4 个 AFLP 的重组率与性别无关,为 0%。使用这些 AFLP 序列对 X. tropicalis 基因组进行 BLASTn 搜索,结果鉴定出了与性别相关的支架。在这些支架的区域中搜索了其他可以用于基因分型的多态性。制定了将基因分型性别纳入以 Xenopus tropicalis 为模型的内分泌干扰物生物测定的回顾性和前瞻性策略。将分析数据作为性别比例变化与使用基因分型评估性别反转的比较的蒙特卡罗模拟表明,通过在研究性腺分化改变时进行基因分型,可获得统计能力的提高。这种识别与性别相关的标记和开发性别基因分型方法的方法适用于具有遗传性别决定的其他物种。