Genomic imprinting and the evolutionary psychology of human kinship

被引:20
|
作者
Haig, David [1 ]
机构
[1] Harvard Univ, Dept Organism & Evolutionary Biol, Cambridge, MA 02138 USA
关键词
father absence; helper-at-the-nest; menarche; kith; divorce; PARENT-OFFSPRING CONFLICT; SILVER-RUSSELL-SYNDROME; PRADER-WILLI-SYNDROME; LIFE-HISTORY; MENARCHEAL AGE; FATHER ABSENCE; GROWTH; CHILDREN; TRANSITION; DEMOGRAPHY;
D O I
10.1073/pnas.1100295108
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Genomic imprinting is predicted to influence behaviors that affect individuals to whom an actor has different degrees of matrilineal and patrilineal kinship (asymmetric kin). Effects of imprinted genes are not predicted in interactions with nonrelatives or with individuals who are equally related to the actor's maternally and paternally derived genes (unless a gene also has pleiotropic effects on fitness of asymmetric kin). Long-term mating bonds are common in most human populations, but dissolution of marriage has always affected a significant proportion of mated pairs. Children born in a new union are asymmetric kin of children born in a previous union. Therefore, the innate dispositions of children toward parents and sibs are expected to be sensitive to cues of marital stability, and these dispositions may be subject to effects of imprinted genes.
引用
收藏
页码:10878 / 10885
页数:8
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