Characterization of the intronic VNTR polymorphisms found in a paralog of chicken serotonin transporter gene

Polymorphisms in the neurotransmitter‐related genes can be a major source of behavioral variations. We searched for polymorphic sites in chicken neurotransmitter‐related genes and identified two variable number of tandem repeat (VNTR) loci encompassing the paralog of chicken serotonin transporter ge...

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Published inAnimal science journal Vol. 84; no. 4; pp. 281 - 288
Main Authors Abe, Hideaki, Takeuchi, Hiro-aki, Yamada, Satoko, Nakamura, Akihiro, Nagao, Kenji, Nirasawa, Keijiro, Ito, Shin'ichi, Inoue-Murayama, Miho
Format Journal Article
LanguageEnglish
Published Australia Blackwell Publishing Ltd 01.04.2013
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Summary:Polymorphisms in the neurotransmitter‐related genes can be a major source of behavioral variations. We searched for polymorphic sites in chicken neurotransmitter‐related genes and identified two variable number of tandem repeat (VNTR) loci encompassing the paralog of chicken serotonin transporter gene (5‐HTT). Both intronic VNTR were highly polymorphic across chicken breeds and the other Galliformes species, even though predominant alleles were considerably different among breeds. One VNTR locus contained sequences complementary to a conserved motif of CCCTC‐binding factor (CTCF) within each repetitive unit, indicating that transcription of chicken 5‐HTT paralog may be regulated by the CTCF protein. It is of great interest to contrast these results with previous knowledge on the human 5‐HTT that also has CTCF binding sites in the repetitive units of intronic VNTR. Additionally, we measured the degree of impulsiveness in domestic chicks for their preference of immediate/small to large/delayed rewards. A significant difference in the impulsiveness score was detected between two chicken breeds (White Leghorn vs. Boris Brown; P < 0.01), as well as between White Leghorn chicks with different 5‐HTT genotypes. These findings imply the possibility that 5‐HTT VNTR genotypes may have some impact on chicks' impulsive choice by modifying the serotonergic neurotransmission.
Bibliography:Kyoto University
Ministry of Education, Culture, Sports, Science and Technology
Figure S1 Principle of impulsiveness measurement (a). A green bead (circled G) means that no reward is given by pecking. The chicks who peck a blue bead (circled B) are immediately rewarded with a small mealworm, whereas a large mealworm is given after 1-s delay by pecking a red bead (circled R). Each chick is subjected to a total of 40 trials, and the ratio of the number of blue beads that are chosen in 10 blue/red trials represents the impulsive score of each individual (b).Figure S2 Amino acid comparison between vertebrate SLC6A4 and chicken slc6a4b (LOC427700). Dots and dashes indicate the identical amino acid residues with consensus and alignment gaps, respectively. Twelve transmembrane regions are highlighted with gray background. Abbreviations and accession numbers are as follows: Homo (Homo sapiens; NP001036), Canis (Canis lupus familiaris; NP001104241), Bos (Bos taurus; NP777034), Mus (Mus musculus; NP034614) and Gallus (Gallus gallus; NP998737).Figure S3 Sequence alignment of chicken slc6a4bin2 with the other species of Galliformes. Dots and dashes indicate the identical nucleotides with consensus and alignment gaps, respectively. The underlines show the flanking sequences of exons. The most conserved regions of potential CTCF binding sites are highlighted. The chicken sequences of slc6a4bin2 (5) and slc6a4bin2 (2) represent the alleles carrying different repeat numbers (5 and 2 copies of a repeat, respectively). Abbreviations and accession numbers are as follows: chukar partridge (Chukar; AB612230), Indian peafowl (Peafowl; AB612231), helmeted guineafowl (Gfowl; AB612232), Himalayan monal (HMonal; AB612233), common pheasant (CPheasant; AB612234), and Japanese quail (Quail; AB612235).
ArticleID:ASJ12011
istex:78189932A95C8C3946AB59DF6EFA1DBD2B0BD61D
ark:/67375/WNG-L9V8TT32-Q
ISSN:1344-3941
1740-0929
DOI:10.1111/asj.12011