A leadership personality type occurs in individuals with two long forms of transporter region (5-HTTLPR) of the serotonin transporter gene.
5-HTTLPR (serotonin-transporter-linked polymorphic region) is a degenerate repeatpolymorphic region in SLC6A4, the gene that codes for the serotonin transporter.
Since the polymorphism was identified in the middle of the 1990s,[1][2]
it has been extensively investigated, e.g., in connection with neuropsychiatric disorders.
A 2006 scientific article stated that "over 300 behavioral, psychiatric, pharmacogenetic and other medical genetics papers" had analyzed the polymorphism.[3]
The serotonin transporter gene (SLC6A4) with the 5-HTTLPR is located on chromosome 17.
The polymorphism occurs in the promoter region of the gene.
Researchers commonly report it with two variations: A short ("s") and a long ("l"), but it can be subdivided further.[4]
In connection with the region are two single nucleotide polymorphisms (SNP): rs25531 and rs25532.[5]
One study published in 2000 found 14 allelic variants (14-A, 14-B, 14-C, 14-D, 15, 16-A, 16-B, 16-C, 16-D, 16-E, 16-F, 19, 20 and 22) in a group of around 200 Japanese and Caucasian people.[4]
The difference between 16-A and 16-D is the rs25531 SNP.
It is also the difference between 14-A and 14-D.[3]
Some studies have found that long allele results in higher serotonin transporter mRNA transcription in human cell lines.
The higher level may be due to the A-allele of rs25531, such that subjects with the long-rs25531(A) allelic combination (sometimes written LA) have higher levels while long-rs25531(G) carriers have levels more similar to short-allele carriers.
Newer studies examining the effects of genotype may compare the LA/LA genotype against all other genotypes.[6] The allele frequency of this polymorphism seems to vary considerably across populations, with a higher frequency of the long allele in Europe and lower frequency in Asia.[7]
In a recent study, authors found that individuals homozygous for the long allele of 5-HTLPR paid more attention on average to positive affective pictures while selectively avoiding negative affective pictures presented alongside the positive pictures compared to their heterozygous and short-allele-homozygous peers. This biased attention of positive emotional stimuli suggests they may tend to be more optimistic.[8] Other research indicates carriers of the short 5-HTTLPR allele have difficulty disengaging attention from emotional stimuli compared to long allele homozygotes.[9] Another recent study using an eye tracking assessment of information processing found that short 5-HTTLPR allele carriers displayed an eye gaze bias to view positive scenes and avoid negative scenes. Long allele homozygotes viewed the emotion scenes in a more even-handed fashion.[10] This research suggests that short 5-HTTLPR allele carriers may be more sensitive to emotional information in the environment than long allele homozygotes.
↑Eisenberg DTA, Hayes MG (2011). "Testing the null hypothesis: comments on “Culture-gene coevolution of individualism-collectivism and the serotonin transporter gene”". Proceedings of the Royal Society B: Biological Sciences278 (1704): 329–332. doi:10.1098/rspb.2010.0714.