Journal of Animal and Veterinary Advances
Year:
2011
Volume:
10
Issue:
4
Page No.
495 - 501
References
Ahituv, N., N. Kavaslar, W. Schackwitz, A. Ustaszewska and J. Martin
et al., 2007. Medical sequencing at the extremes of human body mass. Am. J. Hum. Genet., 80: 779-791.
CrossRef | Capon, F., M.H. Allen, M. Ameen, A.D. Burden, D. Tillman, J.N. Barkerand and R.C. Trembath, 2004. A synonymous SNP of the corneodesmosin gene leads to increased mRNA stability and demonstrates association with psoriasis across diverse ethnic groups. Hum. Mol. Genet., 13: 2361-2368.
CrossRef | Chamary, J.V. and L.D. Hurst, 2005. Evidence for selection on synonymous mutations affecting stability of mRNA secondary structure in mammals. Genome. Biol., 6: R75-R75.
CrossRef | Chen, H., R. Chrast, C. Rossier, A. Gos and S.E. Antonarakisis
et al., 1995. Single-minded and downs syndrome. Nat. Genet., 10: 9-10.
Duan, J., M.S. Wainwright, J.M. Comeron, N. Saitou, A.R. Sanders, J. Gelernter and P.V. Gejman, 2003. Synonymous mutations in the human
Dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor. Hum. Mol. Genet., 12: 205-216.
CrossRef | Eaton, J.L. and E. Glasgow, 2006. The zebrafish bHLH-PAS transcriptional regulator, single-minded 1 (
SIM1), is required for isotocin cell development. Dev. Dynam., 235: 2071-2082.
Direct Link | Ema, M., M. Suzuki, M. Morita, K. Hirose and K. Sogawa
et al., 1996. CDNA cloning of a murine homologue of
Drosophila single-minded, its mRNA expression in mouse development and chromosome localization. Biochem. Biophys. Res. Commun., 218: 588-594.
PubMed | Erbel, P.J., P.B. Card, O. Karakuzu, R.K. Bruick and K.H. Gardner, 2003. Structural basis for PAS domain heterodimerization in the basic helix-loop-helix-PAS transcription factor hypoxia-inducible factor. Proc. Natl. Acad. Sci. USA., 100: 15504-15509.
PubMed | Geldermann, H., E. Muller, G. Moser, G. Reiner and H. Bartenschlager
et al., 2003. Genome wide linkage and QTL mapping in porcine F2 families generated from Pietrain, Meishan and Wild Boar crosses. J. Anim. Breed. Genet., 120: 363-393.
CrossRef | Gilhuis, H.J., C.M. van Ravenswaaij, B.J. Hamel and F.J. Gabreels, 2000. Interstitial 6q deletion with a prader-willi-like phenotype: A new case and review of the literature. Eur. J. Paediatr. Neurol., 4: 39-43.
CrossRef | Holder, J.L., L. Jr. Zhang, B.M. Kublaoui, R.J. DiLeone and O.K. Oz
et al., 2004.
SIM1 gene dosage modulates the homeostatic feeding response to increased dietary fat in mice. Am. J. Physiol. Endocrinol. Metab., 287: E105-E113.
CrossRef | Hollander, E., S. Novotny, M. Hanratty, R. Yaffe, C.M. DeCaria, B.R. Aronowritz and S. Mosovich, 2003. Oxytocin infusion reduces repetitive behaviors in adults with autistic and aspergers disorders. Neuropsychopharmacology, 28: 193-198.
PubMed | Huang, Z.J., I. Edery and M. Rosbash, 1993. PAS is a dimerization domain common to Drosophila period and several transcription factors. Nature, 364: 259-262.
PubMed | Hung, C.C., J. Luan, M. Sims, J.M. Keogh and C. Hall
et al., 2007. Studies of the
SIM1 gene in relation to human obesity and obesity-related traits. Int. J. Obes., 31: 429-434.
CrossRef | PubMed | Insel, T.R., D.J. O'Brien and J.F. Leckman, 1999. Oxytocin, vasopressin and autism: Is there a connection. Biol. Psychiatry, 45: 145-157.
CrossRef | Kobayashi, E., H. Hasebe, K. Kuchida, T. Kawamura, T. Okumura and T. Abe, 2009. Detection of DNA polymorphisms in the MSTN gene and the effect of F94L on meat quantity and quality traits in Japanese black x limousin F2 population. J. Anim. Vet. Adv., 8: 1609-1615.
CrossRef | Direct Link | Kublaoui, B.M., J.L. Jr. Holder, K.P. Tolson, T. Gemelli and A.R. Zinn, 2006.
SIM1 overexpression partially rescues agouti yellow and diet-induced obesity by normalizing food intake. Endocrinology, 147: 4542-4549.
CrossRef | Kumar, S., K. Tamura and M. Nei, 2004. MEGA
3: Integrated software for molecular evolutionary genetics analysis and sequence alignment. Brief. Bioinform., 5: 150-163.
CrossRef | PubMed | Direct Link | Liu, Y., X. Lu, Y.R. Luo, J.P. Zhou, X.Y. Liu, Q. Zhang and Z.J. Yin, 2009. Effect of single nucleotide polymorphism of IRF1 gene on cytokine traits in three pig breeds. J. Anim. Vet. Adv., 18: 2346-2350.
CrossRef | Direct Link | Michaud, J.L., F. Boucher, A. Melnyk, F. Gauthier and E. Goshu
et al., 2001.
SIM1 haploinsufficiency causes hyperphagia, obesity and reduction of the paraventricular nucleus of the hypothalamus. Hum. Mol. Genet., 10: 1465-1473.
CrossRef | Michuad, J.L., T. Rosenquist, N.R. May and C.M. Fan, 1998. Development of neuroendocrine lineages requires the bHLH-PAS transcription factor
SIM1. Genes. Dev., 12: 3264-3275.
CrossRef | Nezer, C., L. Moreau, D. Wagenaar and M. Georges, 2002. Results of a whole genome scan targeting QTL for growth and carcass traits in a Pietrain x Large White intercross. Genet. Sel. Evol., 34: 371-387.
CrossRef | Swaab, D.F., J.S. Purba and M.A. Hofman, 1995. Alterations in the hypothalamic paraventricular nucleus and its oxytocin neurons (putative satiety cells) in Prader-Willi Syndrome: A study of five cases. J. Clin. Endocrinol. Metab., 80: 573-579.
PubMed | Tolson, K.P., T. Gemelli, L. Gautron, J.K. Elmquist, A.R. Zinn and B.M. Kublaoui, 2010. Postnatal
SIM1 deficiency cause hyperphagic obesity and reduced
Mc4r and
Oxytocin expression. J. Neurosci., 30: 3803-3812.
CrossRef | Traurig, M., J. Mack, R.L. Hanson, M. Ghoussaini and D. Meyre
et al., 2009. Common variation in
SIM1 is reproducibly associated with BMI in Pima Indians. Diabetes, 58: 1682-1689.
CrossRef | Varela, M.C., A.Y. Simooes-Sato, C.A. Kim, D.R. Bertola, C.I. de Castro and C.P. Koiffman, 2006. A new case of interstitial 6q16.2 deletion in a patient with prader-willi-like phenotype and investigation of
SIM1 gene deletion in 87 patients with syndromic obesity. Eur. J. Med. Genet., 49: 298-305.
CrossRef | Visscher, P., R. Pong-Wong, C. Whittemore and C. Haley, 2000. Impact of biotechnology on (cross) breeding programmes in pigs. Livest. Prod. Sci., 65: 57-70.
CrossRef | Woods, S.L. and M.L. Whitelaw, 2002. Differential activities of murine single minded 1 (
SIM1) and
SIM2 on a hypoxic response element. Cross-talk between basic helix-loop-helix/per-Arnt-Sim homology transcription factors. J. Biol. Chem., 277: 10236-10243.
PubMed | Yamaki, A., S. Noda, J. Kudoh, N. Shindoh and H. Maeda
et al., 1996. The mammalian single-minded (
SIM) gene: Mouse cDNA structure and diencephalic expression indicate a candidate gene for down syndrome. Genomics, 35: 136-143.
PubMed | Zhao, X.F., N.Y. Xu, Z. Chen, Q. Wang and X.L. Guo, 2008. Single-minded 1 gene mapping and its variants association with growth, carcass composition and meat quality traits in pig. Asian-Aust. J. Anim., 21: 941-946.
Direct Link |