Conjugated linoleic acid synthesis-related protein proteasome subunit α 5 (PSMA5) is increased by vaccenic acid treatment in goat mammary tissue

Journal of Dairy Science

Volumn 95, Issue 8, 2012, Pages 4286-4297

  Jin, Y C ^a,b   Li, Z H ^c   Hong, Z S ^d   Xu, C X ^e   Han, J A ^c   Choi, S H ^f   Yin, J L ^c   Zhang, Q K ^c   Lee, K B ^g   Kang, S K ^c   Song, M K ^h   Kim, Y J ⁱ   Kang, H S ^b   Choi, Y J ^c   Lee, H G ^b  

^a JILIN UNIVERSITY   (China)

^b Pusan National University   (South Korea)

^c Seoul National University   (South Korea)

^d TIANJIN AGRICULTURAL UNIVERSITY   (China)

^e H LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE   (United States)

^f TEXAS A AND M UNIVERSITY   (United States)

^g SongDo Techno Park ^*  (South Korea)

^h Chungbuk National University   (South Korea)

ⁱ Korea University   (South Korea)

Author keywords

type 5 (PSMA5); Conjugated linoleic acid biosynthesis; Macropain) subunit; Mammary tissue; Proteasome (prosome; Two dimensional gel electrophoresis

Indexed keywords

11-OCTADECENOIC ACID; CONJUGATED LINOLEIC ACID; OLEIC ACID; RNA; VACCENIC ACID;

ANIMAL; ANIMAL DISEASE; ARTICLE; CATTLE; CELL LINE; CHEMISTRY; ELECTROSPRAY MASS SPECTROMETRY; FEMALE; GENETICS; GOAT; METABOLISM; MILK; REAL TIME POLYMERASE CHAIN REACTION; TWO DIMENSIONAL GEL ELECTROPHORESIS; UDDER; WESTERN BLOTTING;

ANIMALS; BLOTTING, WESTERN; CATTLE; CELL LINE; ELECTROPHORESIS, GEL, TWO-DIMENSIONAL; FEMALE; GOATS; LINOLEIC ACIDS, CONJUGATED; MAMMARY GLANDS, ANIMAL; MILK; OLEIC ACIDS; REAL-TIME POLYMERASE CHAIN REACTION; RNA; SPECTROMETRY, MASS, ELECTROSPRAY IONIZATION;

ANIMALIA; BOVINAE; CAPRA HIRCUS;

EID: 84864050963     PISSN: 00220302     EISSN: 15253198     Source Type: Journal    
DOI: 10.3168/jds.2011-4281     Document Type: Article

References (68)

1. Adlof R.O., Duval S., Emken E.A. Biosynthesis of conjugated linoleic acid in humans. Lipids 2000, 35:131-135.
2. Aksu S., Scheler C., Focks N., Leenders F., Theuring F., Salnikow J., Jungblut P.R. An iterative calibration method with prediction of post-translational modifications for the construction of a two-dimensional electrophoresis database of mouse mammary gland proteins. Proteomics 2002, 2:1452-1463.
3. Official Methods of Analysis 1995, AOAC, Association of Official Analytical Chemists, Washington, DC. 16th.
4. Arlt A., Bauer I., Schafmayer C., Tepel J., Müerköster S.S., Brosch M., Röder C., Kalthoff H., Hampe J., Moyer M.P., Fölsch U.R., Schäfer H. Increased proteasome subunit protein expression and proteasome activity in colon cancer relate to an enhanced activation of nuclear factor E2-related factor 2 (Nrf2). Oncogene 2009, 28:3983-3996.
5. Aro A., Männistö S., Salminen I., Ovaskainen M.L., Kataja V., Uusitupa M. Inverse association between dietary and serum conjugated linoleic acid and risk of breast cancer in postmenopausal women. Nutr. Cancer 2000, 38:151-157.
6. Banni S., Angioni E., Murru E., Carta G., Melis M.P., Bauman D., Dong Y., Ip C. Vaccenic acid feeding increases tissue levels of conjugated linoleic acid and suppresses development of premalignant lesions in rat mammary gland. Nutr. Cancer 2001, 41:91-97.
7. Bauman D.E., Corl B.A., Baumgard L.H., Griinari J.M. Conjugated linoleic acid (CLA) and the dairy cow. Recent Advances in Animal Nutrition 2001, 237-266. Nottingham University Press, Nottingham, UK. P.C. Garnsworthy, D.J. Cole (Eds.).
8. Bernard L., Leroux C., Chilliard Y. Expression and nutritional regulation of lipogenic genes in the ruminant lactating mammary gland. Adv. Exp. Med. Biol. 2008, 606:67-108.
9. Bickerstaffe R., Annison E.F. Lipid metabolism in the perfused chicken liver. The uptake and metabolism of oleic acid, elaidic acid, cis-vaccenic acid, trans-vaccenic acid and stearic acid. Biochem. J. 1970, 118:433-442.
10. Blankson H., Stakkestad J.A., Fagertun H., Thom E., Wadstein J., Gudmundsen O. Conjugated linoleic acid reduces body fat mass in overweight and obese humans. J. Nutr. 2000, 130:2943-2948.
11. Corl B.A., Barbano D.M., Bauman D.E., Ip C. cis-9,trans-11 CLA derived endogenously from trans-11 18:1 reduces cancer risk in rats. J. Nutr. 2003, 133:2893-2900.
12. Corl B.A., Baumgard L.H., Dwyer D.A., Griinari J.M., Phillips B.S., Bauman D.E. The role of delta(9)-desaturase in the production of cis-9,trans-11 CLA. J. Nutr. Biochem. 2001, 12:622-630.
13. de Roos B., Rucklidge G., Reid M., Ross K., Duncan G., Navarro M.A., Arbones-Mainar J.M., Guzman-Garcia M.A., Osada J., Browne J., Loscher C.E., Roche H.M. Divergent mechanisms of cis9, trans11-and trans10, cis12-conjugated linoleic acid affecting insulin resistance and inflammation in apolipoprotein E knockout mice: A proteomics approach. FASEB J. 2005, 19:1746-1748.
14. Desrivières S., Prinz T., Castro-Palomino L.N., Meyer M., Boehm G., Bauer U., Schäfer J., Neumann T., Shemanko C., Groner B. Comparative proteomic analysis of proliferating and functionally differentiated mammary epithelial cells. Mol. Cell. Proteomics 2003, 2:1039-1054.
15. Desterro J.M., Rodriguez M.S., Hay R.T. Regulation of transcription factors by protein degradation. Cell. Mol. Life Sci. 2000, 57:1207-1219.
16. Folch J., Lees M., Sloane Stanley G.H. A simple method for the isolation and purification of total lipids from animal tissues. J. Biol. Chem. 1957, 226:497-509.
17. Griinari J.M., Corl B.A., Lacy S.H., Chouinard P.Y., Nurmela K.V., Bauman D.E. Conjugated linoleic acid is synthesized endogenously in lactating dairy cows by delta(9)-desaturase. J. Nutr. 2000, 130:2285-2291.
18. Hayek M.G., Han S.N., Wu D., Watkins B.A., Meydani M., Dorsey J.L., Smith D.E., Meydani S.N. Dietary conjugated linoleic acid influences the immune response of young and old C57BL/6NCrlBR mice. J. Nutr. 1999, 129:32-38.
19. Heinemann F.S., Ozols J. Degradation of stearoyl-coenzyme A desaturase: Endoproteolytic cleavage by an integral membrane protease. Mol. Biol. Cell 1998, 9:3445-3453.
20. Hilt W., Wolf D.H. Proteasomes: Destruction as a programme. Trends Biochem. Sci. 1996, 21:96-102.
21. Hirano Y., Hayashi H., Iemura S., Hendil K.B., Niwa S., Kishimoto T., Kasahara M., Natsume T., Tanaka K., Murata S. Cooperation of multiple chaperones required for the assembly of mammalian 20S proteasomes. Mol. Cell 2006, 24:977-984.
22. Hirano Y., Hendil K.B., Yashiroda H., Iemura S., Nagane R., Hioki Y., Natsume T., Tanaka K., Murata S. A heterodimeric complex that promotes the assembly of mammalian 20S proteasomes. Nature 2005, 437:1381-1385.
23. Hochstrasser M. Protein degradation or regulation: Ub the judge. Cell 1996, 84:813-815.
24. Houseknecht K.L., Vanden Heuvel J.P., Moya-Camarena S.Y., Portocarrero C.P., Peck L.W., Nickel K.P., Belury M.A. Dietary conjugated linoleic acid normalizes impaired glucose tolerance in the Zucker diabetic fatty fa/fa rat. Biochem. Biophys. Res. Commun. 1998, 244:678-682.
25. Huynh H.T., Robitaille G., Turner J.D. Establishment of bovine mammary epithelial cells (MAC-T): An in vitro model for bovine lactation. Exp. Cell Res. 1991, 197:191-199.
26. Jayan G.C., Herbein J.H. " Healthier" dairy fat using trans-vaccenic acid. Nutr. Food Sci. 2000, 30:304-309.
27. Jin Y.C., Lee H.G., Xu C.X., Han J.A., Choi S.H., Song M.K., Kim Y.J., Lee K.B., Kim S.K., Kang H.S., Cho B.W., Shin T.S., Choi Y.J. Proteomic analysis of endogenous conjugated linoleic acid biosynthesis in lactating rats and mouse mammary gland epithelia cells (HC11). Biochim. Biophys. Acta 2010, 1804:745-751.
28. Kato H., Sakaki K., Mihara K. Ubiquitin-proteasome-dependent degradation of mammalian ER stearoyl-CoA desaturase. J. Cell Sci. 2006, 119:2342-2353.
29. Kim E.J., Kim W.Y., Kang Y.H., Ha Y.L., Bach L.A., Park J.H.Y. Inhibition of Caco-2 cell proliferation by (n-3) fatty acids: Possible mediation by increased secretion of insulin-like growth factor binding protein-6. Nutr. Res. 2000, 20:1409-1421.
30. King R.W., Deshaies R.J., Peters J.M., Kirschner M.W. How proteolysis drives the cell cycle. Science 1996, 274:1652-1659.
31. Kinsella J.E. Stearic acid metabolism by mammary cells. J. Dairy Sci. 1970, 53:1757-1765.
32. Kraft J., Hanske L., Mockel P., Zimmermann S., Hartl A., Kramer J.K.G., Jahreis G. The conversion efficiency of trans-11 and trans-12 18:1 by delta 9-desaturation differs in rats. J. Nutr. 2006, 136:1209-1214.
33. Kulichkova V.A., Tsimokha A.S., Fedorova O.A., Moiseeva T.N., Bottril A., Lezina L., Gauze L.N., Konstantinova I.M., Mittenberg A.G., Barlev N.A. 26S proteasome exhibits endoribonuclease activity controlled by extra-cellular stimuli. Cell Cycle 2010, 9:840-849.
34. Kusmierczyk A.R., Kunjappu M.J., Funakoshi M., Hochstrasser M. A multimeric assembly factor controls the formation of alternative 20S proteasomes. Nat. Struct. Mol. Biol. 2008, 15:237-244.
35. Le Tallec B., Barrault M.B., Courbeyrette R., Guérois R., Marsolier-Kergoat M.C., Peyroche A. 20S proteasome assembly is orchestrated by two distinct pairs of chaperones in yeast and in mammals. Mol. Cell 2007, 27:660-674.
36. Lee K.N., Kritchevsky D., Pariza M.W. Conjugated linoleic acid and atherosclerosis in rabbits. Atherosclerosis 1994, 108:19-25.
37. Lengi A.J., Corl B.A. Identification and characterization of a novel bovine stearoyl-CoA desaturase isoform with homology to human SCD5. Lipids 2007, 42:499-508.
38. Livak K.J., Schmittgen T.D. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-delta delta C(T)) method. Methods 2001, 25:402-408.
39. Lock A.L., Corl B.A., Barbano D.M., Bauman D.E., Ip C. The anticarcinogenic effect of trans-11 18:1 is dependent on its conversion to cis-9, trans-11 CLA by Δ9-desaturase in rats. J. Nutr. 2004, 134:2698-2704.
40. Loor J.J., Ferlay A., Ollier A., Ueda K., Doreau M., Chilliard Y. High-concentrate diets and polyunsaturated oils alter trans and conjugated isomers in bovine rumen, blood, and milk. J. Dairy Sci. 2005, 88:3986-3999.
41. Loor J.J., Lin X., Herbein J.H. Dietary trans-vaccenic acid (trans11-18:1) increases concentration of cis9, trans11-conjugated linoleic acid (rumenic acid) in tissues of lactating mice and suckling pups. Reprod. Nutr. Dev. 2002, 42:85-99.
42. Man W.C., Miyazaki M., Chu K., Ntambi J.M. Membrane topology of mouse stearoyl-CoA desaturase 1. J. Biol. Chem. 2006, 281:1251-1260.
43. Matitashvili E., Bauman D.E. Effect of different isomers of C18:1 and C18:2 fatty acids on lipogenesis in bovine mammary epithelial cells. J. Anim. Sci. 2000, 83(Suppl. 1):165. (Abstr.).
44. Matlack K.E.S., Mothes W., Rapoport T.A. Protein translocation: Tunnel vision. Cell 1998, 92:381-390.
45. McDonald T.M., Kinsella J.E. Stearyl-CoA desaturase of bovine mammary microsomes. Arch. Biochem. Biophys. 1973, 156:223-231.
46. Morrison W.R., Smith L.M. Preparation of fatty acid methyl esters and dimethylacetals from lipids with boron fluoride-methanol. J. Lipid Res. 1964, 5:600-608.
47. Mosley E.E., McGuire M.K., Williams J.E., McGuire M.A. cis-9, trans-11 conjugated linoleic acid is synthesized from vaccenic acid in lactating women. J. Nutr. 2006, 136:2297-2301.
48. Mosley E.E., Shafii Dagger B., Moate P.J., McGuire M.A. cis-9, trans-11 conjugated linoleic acid is synthesized directly from vaccenic acid in lactating dairy cattle. J. Nutr. 2006, 136:570-575.
49. Murata S., Yashiroda H., Tanaka K. Molecular mechanisms of proteasome assembly. Nat. Rev. Mol. Cell Biol. 2009, 10:104-115.
50. Mziaut H., Korza G., Ozols J. The N-terminus of microsomal delta 9 stearoyl-CoA desaturase contains the sequence determinant for its rapid degradation. Proc. Natl. Acad. Sci. USA 2000, 97:8883-8888.
51. Nutrient Requirements of Small Ruminants: Sheep, Goats, Cervids, and New World Camelids 2007, NRC, National Academies Press, Washington, DC.
52. Ntambi J.M. The regulation of stearoyl-CoA desaturase (SCD). Prog. Lipid Res. 1995, 34:139-150.
53. Oikawa T., Sasaki T., Nakamura M., Shimamura M., Tanahashi N., Omura S., Tanaka K. The proteasome is involved in angiogenesis. Biochem. Biophys. Res. Commun. 1998, 246:243-248.
54. Orlowski R.Z. The role of the ubiquitin-proteasome pathway in apoptosis. Cell Death Differ. 1999, 6:303-313.
55. Oshino N., Sato R. The dietary control of the microsomal stearyl CoA-desaturation enzyme system in rat liver. Arch. Biochem. Biophys. 1972, 149:369-377.
56. Ozols J. Degradation of hepatic stearyl CoA delta 9-desaturase. Mol. Biol. Cell 1997, 8:2281-2290.
57. Paton C.M., Ntambi J.M. Biochemical and physiological function of stearoyl-CoA desaturase. Am. J. Physiol. Endocrinol. Metab. 2009, 297:E28-E37.
58. Pollard M.R., Gunstone F.D., James A.T., Morris L.J. Desaturation of positional and geometric isomers of monoenoic fatty acids by microsomal preparations from rat liver. Lipids 1980, 15:306-314.
59. Read M.A., Neish A.S., Luscinskas F.W., Palombella V.J., Maniatis T., Collins T. The proteasome pathway is required for cytokine-induced endothelial-leukocyte adhesion molecule expression. Immunity 1995, 2:493-506.
60. Sakamoto K., Sato Y., Shinka T., Sei M., Nomura I., Umeno M., Ewis A.A., Nakahori Y. Proteasome subunits mRNA expressions correlate with male BMI: Implications for a role in obesity. Obesity (Silver Spring) 2009, 17:1044-1049.
61. Salminen I., Mutanen M., Jauhiainen M., Aro A. Dietary trans fatty acids increase conjugated linoleic acid levels in human serum. J. Nutr. Biochem. 1998, 9:93-98.
62. Santora J.E., Palmquist D.L., Roehrig K.L. Trans-vaccenic acid is desaturated to conjugated linoleic acid in mice. J. Nutr. 2000, 130:208-215.
63. Shevchenko A., Jensen O.N., Podtelejnikov A.V., Sagliocco F., Wilm M., Vorm O., Mortensen P., Shevchenko A., Boucherie H., Mann M. Linking genome and proteome by mass spectrometry: Large-scale identification of yeast proteins from two-dimensional gels. Proc. Natl. Acad. Sci. USA 1996, 93:14440-14445.
64. Turpeinen A.M., Mutanen M., Aro A., Salminen I., Basu S., Palmquist D.L., Griinari J.M. Bioconversion of vaccenic acid to conjugated linoleic acid in humans. Am. J. Clin. Nutr. 2002, 76:504-510.
65. Viswanadha S., Giesy J.G., Hanson T.W., McGuire M.A. Dose response of milk fat to intravenous administration of the trans-10, cis-12 isomer of conjugated linoleic acid. J. Dairy Sci. 2003, 86:3229-3236.
66. Ward R.J., Travers M.T., Richards S.E., Vernon R.G., Salter A.M., Buttery P.J., Barber M.C. Stearoyl-CoA desaturase mRNA is transcribed from a single gene in the ovine genome. Biochem. Biophys. Acta 1998, 1391:145-156.
67. Yashiroda H., Mizushima T., Okamoto K., Kameyama T., Hayashi H., Kishimoto T., Niwa S., Kasahara M., Kurimoto E., Sakata E., Takagi K., Suzuki A., Hirano Y., Murata S., Kato K., Yamane T., Tanaka K. Crystal structure of a chaperone complex that contributes to the assembly of yeast 20S proteasomes. Nat. Struct. Biol. Mol. 2008, 15:228-236.
68. Zhou Y., Akers R.M., Jiang H. Growth hormone can induce expression of four major milk protein genes in transfected MAC-T cells. J. Dairy Sci. 2008, 91:100-108.