Manno Francis Anthony Michael
Department of Biology, Virginia Wesleyan College, Norfolk, Va 23502-5599, USA.
Physiol Behav. 2008 Jan 28;93(1-2):364-8. doi: 10.1016/j.physbeh.2007.09.011. Epub 2007 Sep 26.
In humans, research has demonstrated the ratio of the 2nd to 4th digit lengths (2D:4D) are: (i) sexually dimorphic with males having a lower ratio than females, the latter having near equidistant lengths [J. Manning, D. Scutt, J. Wilson, & D. Lewis-Jones, (1998). The ratio of 2nd to 4th digit length: a predictor of sperm numbers and concentrations of testosterone, luteinizing hormone and oestrogen. Hum Reprod. 13(11):3000-3004], and are theorized to be (ii) determined in utero during gestational development [J. Manning, & P. Bundred, (2000). The ratio of 2nd to 4th digit length: a new predictor of disease predisposition? Med Hypotheses. 54(5):855-857], and (iii) correlated with prenatal androgen levels [J. Manning, & P. Bundred, (2000). The ratio of 2nd to 4th digit length: a new predictor of disease predisposition? Med Hypotheses. 54(5):855-857; J. Manning, R. Trivers, D. Singh, & R. Thornhill, (1999). The mystery of female beauty. Nature. 399:214-215; T. Williams, M. Pepitone, S. Christensen, B. Cooke, A. Huberman, N. Breedlove, et al., (2000). Finger-length ratios and sexual orientation: measuring people's finger patterns may reveal some surprising information. Nature. 404:455-456]. These phenotypes correspond to the hormonal effects of testosterone (i.e. androgens) in utero in both sexes. In mice, testosterone in utero is associated in males and females with the anogenital distance (AGD), a phenotype where AGD is greater in males and females contiguous with two males (2M) have a masculinized AGD phenotype whereas those juxtaposed to fewer males, one or zero (1M or 0M), have a more feminine phenotype, i.e. shorter AGD [F. vom Saal, & F. Bronson, (1980). Sexual characteristics of adult female mice are correlated with their blood testosterone levels during prenatal development. Science. 208:597-599; R. Gandelman, F. vom Saal, & J. Reinisch, (1977). Contiguity to male foetuses affects morphology and behaviour of female mice. Nature. 266:722-724; A. Hotchkiss, & J. Vandenbergh, (2005). The anogenital distance index of mice (Mus musculus domesticus): an analysis. Contem Top Lab Anim Sci. 44(4):46-48; C. Kinsley, J. Miele, C. Wagner, L. Ghiraldi, J. Broida, B. Svare, (1986). Prior intrauterine position influences body weight in male and female mice. Horm Behav. 20:201-211; S. Graham, R. Gandelman, (1986). The expression of ano-genital distance data in the mouse. Physiol Behav. 36(1):103-104; B. Ryan, & J. Vandenbergh, (2002). Intrauterine position effects. Neurosci Biobehav Rev. 26(6):665-678; J. Vandenbergh, & C. Huggett, (1995). The anogenital distance index, a predictor of the intrauterine position effects on reproduction in female house mice. Lab Anim Sci. 45(5):567-573]. Furthermore, in humans AGD is sexually dimorphic with neonate males having a greater distance than females [E. Salazar-Martinez, P. Romano-Riquer, E. Yanez-Marquez, M. Longnecker, M. Hernandez-Avila, (2004). Anogenital distance in human male and female newborns: a descriptive, cross-sectional study. Environmental Health: A Global Access Science Source. 2004:3:(8) (doi:10.1186/1476-069X-3-8) [12]]. Recently, research has concluded that the digit lengths of mice have the same phenotypic pattern seen in humans, with the 2D:4D ratio being sexually dimorphic, i.e. lower in males and greater in females [W. Brown, C. Finn, & S. Breedlove, (2002). Sexual dimorphism in digit-length ratios of laboratory mice. Anat Rec. 267(3):231-234; J. Manning, M. Callow, & P. Bundred, (2003). Finger and toe ratios in humans and mice: implications for the aetiology of diseases influenced by HOX genes. Med Hypotheses. 60(3):340-343; W. Brown, C. Finn, & S. Breedlove, (2001). A sex difference in the digit length ratio in mice. Horm Behav. 39:325]. The following study was conducted to determine whether the digit length ratios in mice are correlated with a known in utero testosterone-dependent effect, the distance from the anus to the genital papilla, the AGD. The results of the experiment demonstrate that there is no correlation between AGD and the 2D:4D ratio in mice of either sex. Furthermore, no sexual dimorphism in the digit lengths was found as opposed to previous studies [W. Brown, C. Finn, & S. Breedlove, (2002). Sexual dimorphism in digit-length ratios of laboratory mice. Anat Rec. 267(3):231-234; J. Manning, M. Callow, & P. Bundred, (2003). Finger and toe ratios in humans and mice: implications for the aetiology of diseases influenced by HOX genes. Med Hypotheses. 60(3):340-343; W. Brown, C. Finn, & S. Breedlove, (2001). A sex difference in the digit length ratio in mice. Horm Behav. 39:325]. Although testosterone has been implicated in the digit length ratios, the present study would suggest that androgens do not have a causal relationship with testosterone-dependent phenotypes [J. Manning, D. Scutt, J. Wilson, & D. Lewis-Jones, (1998). The ratio of 2nd to 4th digit length: a predictor of sperm numbers and concentrations of testosterone, luteinizing hormone and oestrogen. Hum Reprod. 13(11):3000-3004; J. Manning, & P. Bundred, (2000). The ratio of 2nd to 4th digit length: A new predictor of disease predisposition?. Med Hypotheses. 54(5):855-857; J. Manning, R. Trivers, D. Singh, & R. Thornhill, (1999). The mystery of female beauty. Nature. 399:214-215]. The attribution of nature (i.e. genetic) and nurture (i.e. environment) in the development of life (i.e. resultant phenotype) is exceedingly complex and the correlation of one trait to another physical characteristic does not preclude there is a causal relationship.
在人类中,研究表明第二与第四指长度之比(2D:4D)具有以下特点:(i)具有性别二态性,男性的该比例低于女性,后者的两指长度近乎相等[J. 曼宁、D. 斯卡特、J. 威尔逊和D. 刘易斯 - 琼斯,(1998年)。第二与第四指长度之比:精子数量以及睾酮、促黄体生成素和雌激素浓度的预测指标。《人类生殖》。13(11):3000 - 3004],并且从理论上来说,(ii)在孕期发育的子宫内就已确定[J. 曼宁和P. 邦德雷德,(2000年)。第二与第四指长度之比:疾病易感性的新预测指标?《医学假说》。54(5):855 - 857],以及(iii)与产前雄激素水平相关[J. 曼宁和P. 邦德雷德,(2000年)。第二与第四指长度之比:疾病易感性的新预测指标?《医学假说》。54(5):855 - 857;J. 曼宁、R. 特里弗斯、D. 辛格和R. 桑希尔,(1999年)。女性美的奥秘。《自然》。399:214 - 215;T. 威廉姆斯、M. 佩皮托内、S. 克里斯滕森、B. 库克、A. 休伯曼、N. 布雷德洛夫等人,(2000年)。手指长度比例与性取向:测量人们的手指模式可能会揭示一些惊人信息。《自然》。404:455 - 456]。这些表型对应于两性在子宫内睾酮(即雄激素)的激素效应。在小鼠中,子宫内的睾酮与雄性和雌性的肛门生殖距离(AGD)相关,对于这一表型,雄性的AGD更大,与两只雄性相邻的雌性(2M)具有男性化的AGD表型,而与较少雄性相邻的雌性,即与一只或零只雄性相邻(1M或0M),则具有更女性化的表型,即较短的AGD [F. 冯·萨尔和F. 布朗森,(1980年)。成年雌性小鼠的性特征与其产前发育期间的血液睾酮水平相关。《科学》。208:597 - 599;R. 甘德尔曼、F. 冯·萨尔和J.赖尼施,(1977年)。与雄性胎儿相邻会影响雌性小鼠的形态和行为。《自然》。266:722 - 724;A. 霍奇基斯和J. 范登伯格,(2005年)。小鼠(小家鼠)的肛门生殖距离指数:一项分析。《当代实验动物科学主题》。44(4):46 - 48;C. 金斯利、J. 米莱、C. 瓦格纳、L. 吉拉尔迪、J. 布罗伊达、B. 斯瓦尔,(1986年)。先前的子宫内位置会影响雄性和雌性小鼠的体重。《激素与行为》。20:201 - 211;S. 格雷厄姆、R. 甘德尔曼,(1986年)。小鼠肛门生殖距离数据的表达。《生理行为》。36(1):103 - 104;B. 瑞安和J. 范登伯格,(2002年)。子宫内位置效应。《神经科学与行为评论》。26(6):665 - 678;J. 范登伯格和C. 哈格特,(1995年)。肛门生殖距离指数,子宫内位置对雌性家鼠繁殖影响的预测指标。《实验动物科学》。45(5):567 - 573]。此外,在人类中,AGD也具有性别二态性,新生男性的距离比女性更大[E. 萨拉查 - 马丁内斯、P. 罗曼诺 - 里克尔、E. 亚涅斯 - 马尔克斯、M. 朗内克、M. 埃尔南德斯 - 阿维拉,(2004年)。人类男、女新生儿的肛门生殖距离:一项描述性横断面研究。《环境卫生:全球科学资源》。2004:3:(8)(doi:10.1186/1476 - 069X - 3 - 8)[12]]。最近,研究得出结论,小鼠的指长具有与人类相同的表型模式,2D:4D比例具有性别二态性,即雄性较低而雌性较高[W. 布朗、C. 芬恩和S. 布雷德洛夫,(2002年)。实验小鼠指长比例的性别二态性。《解剖学记录》。267(3):231 - 234;J. 曼宁、M. 卡洛和P. 邦德雷德,(2003年)。人类和小鼠的手指与脚趾比例:对受HOX基因影响疾病病因学的启示。《医学假说》。60(3):340 - 343;W. 布朗、C. 芬恩和S. 布雷德洛夫,(2001年)。小鼠指长比例的性别差异。《激素与行为》。39:325]。以下研究旨在确定小鼠的指长比例是否与一种已知的子宫内睾酮依赖性效应,即从肛门到生殖乳头的距离(AGD)相关。实验结果表明,两性小鼠的AGD与2D:4D比例之间均无相关性。此外,与先前的研究不同,未发现指长存在性别二态性[W. 布朗、C. 芬恩和S. 布雷德洛夫,(2002年)。实验小鼠指长比例的性别二态性。《解剖学记录》。267(3):231 - 234;J. 曼宁、M. 卡洛和P. 邦德雷德,(2003年)。人类和小鼠的手指与脚趾比例:对受HOX基因影响疾病病因学的启示。《医学假说》。60(3):340 - 343;W. 布朗、C. 芬恩和S. 布雷德洛夫,(2001年)。小鼠指长比例的性别差异。《激素与行为》。39:325]。尽管睾酮与指长比例有关,但本研究表明雄激素与睾酮依赖性表型之间不存在因果关系[J. 曼宁、D. 斯卡特、J. 威尔逊和D. 刘易斯 - 琼斯,(1998年)。第二与第四指长度之比:精子数量以及睾酮、促黄体生成素和雌激素浓度的预测指标。《人类生殖》。13(11):3000 - 3004;J. 曼宁和P. 邦德雷德,(2000年)。第二与第四指长度之比:疾病易感性的新预测指标?《医学假说》。54(5):855 - 857;J. 曼宁、R. 特里弗斯、D. 辛格和R. 桑希尔,(1999年)。女性美的奥秘。《自然》。399:214 - 215]。在生命发育过程中(即最终表型),自然(即遗传)和 nurture(即环境)的归因极其复杂,一个性状与另一个身体特征的相关性并不排除存在因果关系。