Advertisement

Bai fu mei: China’s obsession with white skin and ‘trophy’ partners may stem from genetic mutation 15,000 years ago, scientists say

New international study led by Chinese team finds the diverging complexions of Han Chinese and native Africans and Southeast Asians was caused by a mutation of the OCA2 gene 15,224 years ago

Reading Time:3 minutes
Why you can trust SCMP
16
Actress Fan Bingbing is one of the hottest female celebrities in China. Chinese internet users employ a portmanteau to describe the most desirable females: Bai-fu-mei puts white (bai) skin color on top of wealth (fu) and beauty (mei). Photo: SCMP Pictures
Stephen Chenin Beijing

Chinese people’s preference for paler or white-coloured skin originates from a “defective” gene, according to an international study led by Chinese scientists.

Advertisement

Men in the country can often seem obsessed with fair skin, especially in a partner, while many women have in the past favoured a Caucasian or “trophy” husband. This has long been dismissed as a social, economic or cultural problem, but new evidence suggests it may stem from a genetic predisposition.

READ MORE: Thai advert for skin lightening pills sparks outrage with tagline ‘white makes you a winner’

For thousands of years, China was ruled by pale-looking nobles in the north, and the invasion of Europeans in its more modern history further added to the perception that a white skin colouring was somehow superior.

But the new study found that the phenomenon could have a biological explanation dating back to prehistoric times as the relatively light skin colouring of the Han Chinese may derive from the same gene held responsible for a number of diseases.

READ MORE: Chinese scientists edit genes to produce artificial sperm capable of creating ‘army of half-cloned mice’

The researchers from China, the United States and Europe analysed genetic samples from more than 1,000 individuals and found that the fairer skin of the Han Chinese in comparison to people from Africa and Southeast Asia was caused by a mutation of the OCA2 gene.

Advertisement