FADS2

Fatty acid desaturase 2 (FADS2) is encoded by the FADS2 gene, the associated enzyme is sometimes known as FADS2 as well.[5][6] Its main associated enzyme is Delta 6 desaturase (D6D) however the human enzyme been shown to also catalyze some delta-8 and delta-4 desaturases in spite of naming conventions.[7]

FADS2
Identifiers
AliasesFADS2, D6D, DES6, FADSD6, LLCDL2, SLL0262, TU13, fatty acid desaturase 2
External IDsOMIM: 606149 MGI: 1930079 HomoloGene: 3149 GeneCards: FADS2
Gene location (Human)
Chr.Chromosome 11 (human)[1]
Band11q12.2Start61,792,980 bp[1]
End61,867,354 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

9415

56473

Ensembl

ENSG00000134824

ENSMUSG00000024665

UniProt

O95864

Q9Z0R9

RefSeq (mRNA)

NM_001281501
NM_001281502
NM_004265

NM_019699

RefSeq (protein)

NP_001268430
NP_001268431
NP_004256

NP_062673

Location (UCSC)Chr 11: 61.79 – 61.87 MbChr 19: 10.06 – 10.1 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Function

Fatty acid desaturase 2 is a member of the fatty acid desaturase (FADS) gene family. Desaturase enzymes cause desaturation of fatty acids through the introduction of double bonds between defined carbons of the fatty acyl chain. FADS family members are considered fusion products composed of an N-terminal cytochrome b5-like domain and a C-terminal multiple membrane-spanning desaturase portion, both of which are characterized by conserved histidine motifs. This gene is clustered with family members FADS1 and FADS2 at 11q12-q13.1; this cluster is thought to have arisen evolutionarily from gene duplication based on its similar exon/intron organization.[5]

Clinical significance

It was reported the FADS2 interacts with breastfeeding such that breast-fed children with the "C" version of the gene appear about 7 intelligence quotient (IQ) points higher than those with the less common "G" version (less than this when adjusted for maternal IQ).[8][9]

An attempt to replicate this study in 5934 8-year-old children failed: No relationship of the common C allele to negative effects of formula feeding was apparent, and contra to the original report, the rare GG homozygote children performed worse when formula fed than other children on formula milk.[10] A study of over 700 families recently found no evidence for either main or moderating effects of the original SNP (rs174575), nor of two additional FADS2 polymorphisms (rs1535 and rs174583), nor any effect of maternal FADS2 status on offspring IQ.[11]

References

  1. GRCh38: Ensembl release 89: ENSG00000134824 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000024665 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. "Entrez Gene: FADS1 fatty acid desaturase 1".
  6. Marquardt A, Stöhr H, White K, Weber BH (June 2000). "cDNA cloning, genomic structure, and chromosomal localization of three members of the human fatty acid desaturase family". Genomics. 66 (2): 175–83. doi:10.1006/geno.2000.6196. PMID 10860662.
  7. "MetaCyc acyl-CoA 4/6/8-desaturase".
  8. Gene governs IQ boost from breastfeeding.
  9. Caspi A, Williams B, Kim-Cohen J, Craig IW, Milne BJ, Poulton R, Schalkwyk LC, Taylor A, Werts H, Moffitt TE (November 2007). "Moderation of breastfeeding effects on the IQ by genetic variation in fatty acid metabolism". Proc. Natl. Acad. Sci. U.S.A. 104 (47): 18860–5. doi:10.1073/pnas.0704292104. PMC 2141867. PMID 17984066.
  10. Steer CD, Davey Smith G, Emmett PM, Hibbeln JR, Golding J (2010). "FADS2 polymorphisms modify the effect of breastfeeding on child IQ". PLOS ONE. 5 (7): e11570. doi:10.1371/journal.pone.0011570. PMC 2903485. PMID 20644632.
  11. Martin NW, Benyamin B, Hansell NK, Montgomery GW, Martin NG, Wright MJ, Bates TC (January 2011). "Cognitive function in adolescence: testing for interactions between breast-feeding and FADS2 polymorphisms". J Am Acad Child Adolesc Psychiatry. 50 (1): 55–62.e4. doi:10.1016/j.jaac.2010.10.010. PMID 21156270.

Further reading

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