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Identification of Differentially Expressed Genes in Bovine Follicular Cystic Ovaries

  • Choe, Chang-Yong (Animal Genetic Resources Station, National Institute of Animal Science, RDA) ;
  • Cho, Young-Woo (Department of Physiology, Institute of Health Sciences, Gyeongsang National University School of Medicine) ;
  • Kim, Chang-Woon (Department of Obstetrics and Gynecology, Samsung Changwon Hospital, Sungkyunkwan University School of Medicine) ;
  • Son, Dong-Soo (Animal Genetic Resources Station, National Institute of Animal Science, RDA) ;
  • Han, Jae-Hee (Department of Physiology, Institute of Health Sciences, Gyeongsang National University School of Medicine) ;
  • Kang, Da-Won (Department of Physiology, Institute of Health Sciences, Gyeongsang National University School of Medicine)
  • Received : 2010.06.02
  • Accepted : 2010.08.25
  • Published : 2010.10.31

Abstract

Follicular cystic ovary (FCO) is one of the most frequently diagnosed ovarian diseases and is a major cause of reproductive failure in mammalian species. However, the mechanism by which FCO is induced remains unclear. Genetic alterations which affect the functioning of many kinds of cells and/or tissues could be present in cystic ovaries. In this study, we performed a comparison analysis of gene expression in order to identify new molecules useful in discrimination of bovine FCO with follicular cystic follicles (FCFs). Normal follicles and FCFs were classified based on their sizes (5 to 10 mm and $\geq25mm$). These follicles had granulosa cell layer and theca interna and the hormone $17{\beta}$-estradiol ($E_2$)/ progesterone ($P_4$) ratio in follicles was greater than one. Perifollicular regions including follicles were used for the preparation of RNA or protein. Differentially expressed genes (DEG) that showed greater than a 2-fold change in expression were screened by the annealing control primer (ACP)-based PCR method using $GeneFishing^{TM}$ DEG kits in bovine normal follicles and FCFs. We identified two DEGs in the FCFs: ribosomal protein L15 (RPL15) and microtubule-associated protein 1B (MAP1B) based on BLAST searches of the NCBI GenBank. Consistent with the ACP analysis, semi-quantitative PCR data and Western blot analyses revealed an up-regulation of RPL15 and a down-regulation of MAP1B in FCFs. These results suggest that RPL15 and MAP1B may be involved in the regulation of pathological processes in bovine FCOs and may help to establish a bovine gene data-base for the discrimination of FCOs from normal ovaries.

Keywords

References

  1. Peter AT. An update on cystic ovarian degeneration in cattle. Reprod Domest Anim. 2004;39:1-7. https://doi.org/10.1046/j.0936-6768.2003.00466.x
  2. Hamilton SA, Garverick HA, Keisler DH, Xu ZZ, Loos K, Youngquist RS, Salfen BE. Characterization of ovarian follicular cysts and associated endocrine profiles in dairy cows. Biol Reprod. 1995;53:890-898. https://doi.org/10.1095/biolreprod53.4.890
  3. Hauptmann S, Denkert C, Koch I, Petersen S, Schluns K, Reles A, Dietel M, Petersen I. Genetic alterations in epithelial ovarian tumors analyzed by comparative genomic hybridization. Hum Pathol. 2002;33:632-641. https://doi.org/10.1053/hupa.2002.124913
  4. Osterberg L, Akeson M, Levan K, Partheen K, Zetterqvist BM, Brannstrom M, Horvath G. Genetic alterations of serous borderline tumors of the ovary compared to stage I serous ovarian carcinomas. Cancer Genet Cytogenet. 2006;167:103-108. https://doi.org/10.1016/j.cancergencyto.2006.01.009
  5. Lingenfelter BM, Dailey RA, Inskeep EK, Vernon MW, Poole DH, Rhinehart JD, Yao J. Microarray analysis of gene expression in granulosal cells from persistent follicles in cattle. Anim Reprod Sci. 2008;104:405-413. https://doi.org/10.1016/j.anireprosci.2007.07.014
  6. Hwang IT, Kim YJ, Kim SH, Kwak CI, Gu YY, Chun JY. Annealing control primer system for improving specificity of PCR amplification. Biotechniques. 2003;35:1180-1184.
  7. Kim YJ, Kwak CI, Gu YY, Hwang IT, Chun JY. Annealing control primer system for identification of differentially expressed genes on agarose gels. Biotechniques. 2004;36:424-426, 428, 430 passim.
  8. Kesler DJ, Elmore RG, Brown EM, Garverick HA. Gonadotropin releasing hormone treatment of dairy cows with ovarian cysts. I. Gross ovarian morphology and endocrinology. Theriogenology. 1981;16:207-217. https://doi.org/10.1016/0093-691X(81)90103-5
  9. Isobe N, Yoshimura Y. Deficient proliferation and apoptosis in the granulosa and theca interna cells of the bovine cystic follicle. J Reprod Dev. 2007;53:1119-1124. https://doi.org/10.1262/jrd.19041
  10. Isobe N, Yoshimura Y. Localization of apoptotic cells in the cystic ovarian follicles of cows: a DNA-end labeling histochemical study. Theriogenology. 2000;53:897-904. https://doi.org/10.1016/S0093-691X(00)00238-7
  11. Calder MD, Manikkam M, Salfen BE, Youngquist RS, Lubahn DB, Lamberson WR, Garverick HA. Dominant bovine ovarian follicular cysts express increased levels of messenger RNAs for luteinizing hormone receptor and 3 beta-hydroxysteroid dehydrogenase delta(4),delta(5) isomerase compared to normal dominant follicles. Biol Reprod. 2001;65:471-476. https://doi.org/10.1095/biolreprod65.2.471
  12. Isobe N, Kitabayashi M, Yoshimura Y. Microvascular distribution and vascular endothelial growth factor expression in bovine cystic follicles. Domest Anim Endocrinol. 2005;29:634-645. https://doi.org/10.1016/j.domaniend.2005.04.007
  13. Nilsson S, Makela S, Treuter E, Tujague M, Thomsen J, Andersson G, Enmark E, Pettersson K, Warner M, Gustafsson JA. Mechanisms of estrogen action. Physiol Rev. 2001;81:1535-1565. https://doi.org/10.1152/physrev.2001.81.4.1535
  14. Matthews J, Gustafsson JA. Estrogen signaling: a subtle balance between ER alpha and ER beta. Mol Interv. 2003;3:281-292. https://doi.org/10.1124/mi.3.5.281
  15. Cochrane AW, Deeley RG. Estrogen-dependent modification of ribosomal proteins. Effects of estrogen withdrawal on the distribution of constitutive and hormonally regulated mRNAs. J Biol Chem. 1984;259:15408-15413.
  16. Sowers JR. Estrogen-inducible cytoskeletal linker protein ezrin interaction with the low-density lipoprotein receptor. Endocrinology. 2004;145:3074. https://doi.org/10.1210/en.2004-0405
  17. Malayer JR, Cheng J, Woods VM. Estrogen responses in bovine fetal uterine cells involve pathways directed by both estrogen response element and activator protein-1. Biol Reprod. 1999;60:1204-1210. https://doi.org/10.1095/biolreprod60.5.1204
  18. Wang Q, Yang C, Zhou J, Wang X, Wu M, Liu Z. Cloning and characterization of full-length human ribosomal protein L15 cDNA which was overexpressed in esophageal cancer. Gene. 2001;263:205-209. https://doi.org/10.1016/S0378-1119(00)00570-9
  19. Wang H, Zhao LN, Li KZ, Ling R, Li XJ, Wang L. Overexpression of ribosomal protein L15 is associated with cell proliferation in gastric cancer. BMC Cancer. 2006;6:91. https://doi.org/10.1186/1471-2407-6-91
  20. Chen FW, Ioannou YA. Ribosomal proteins in cell proliferation and apoptosis. Int Rev Immunol. 1999;18:429-448. https://doi.org/10.3109/08830189909088492
  21. Wool IG. Extraribosomal functions of ribosomal proteins. Trends Biochem Sci. 1996;21:164-165. https://doi.org/10.1016/S0968-0004(96)20011-8
  22. Caetano AR, Johnson RK, Pomp D. Generation and sequence characterization of a normalized cDNA library from swine ovarian follicles. Mamm Genome. 2003;14:65-70. https://doi.org/10.1007/s00335-002-2220-5
  23. Yao J, Ren X, Ireland JJ, Coussens PM, Smith TP, Smith GW. Generation of a bovine oocyte cDNA library and microarray: resources for identification of genes important for follicular development and early embryogenesis. Physiol Genomics. 2004;19:84-92. https://doi.org/10.1152/physiolgenomics.00123.2004
  24. Bettegowda A, Patel OV, Ireland JJ, Smith GW. Quantitative analysis of messenger RNA abundance for ribosomal protein L-15, cyclophilin-A, phosphoglycerokinase, beta-glucuronidase, glyceraldehyde 3-phosphate dehydrogenase, beta-actin, and histone H2A during bovine oocyte maturation and early embryogenesis in vitro. Mol Reprod Dev. 2006;73:267-278. https://doi.org/10.1002/mrd.20333
  25. Vallee RB, Davis SE. Low molecular weight microtubule-associated proteins are light chains of microtubule-associated protein 1 (MAP 1). Proc Natl Acad Sci U S A. 1983;80:1342-1346. https://doi.org/10.1073/pnas.80.5.1342
  26. Bloom GS, Luca FC, Vallee RB. Microtubule-associated protein 1B: identification of a major component of the neuronal cytoskeleton. Proc Natl Acad Sci U S A. 1985;82:5404-5408. https://doi.org/10.1073/pnas.82.16.5404
  27. Binder LI, Frankfurter A, Kim H, Caceres A, Payne MR, Rebhun LI. Heterogeneity of microtubule-associated protein 2 during rat brain development. Proc Natl Acad Sci U S A. 1984;81:5613-5617. https://doi.org/10.1073/pnas.81.17.5613
  28. Cueille N, Blanc CT, Riederer IM, Riederer BM. Microtubule-associated protein 1B binds glyceraldehyde-3-phosphate dehydrogenase. J Proteome Res. 2007;6:2640-2647. https://doi.org/10.1021/pr070081z
  29. Cooley L, Theurkauf WE. Cytoskeletal functions during Drosophila oogenesis. Science. 1994;266:590-596. https://doi.org/10.1126/science.7939713
  30. Uchida Y. Overexpression of full-length but not N-terminal truncated isoform of microtubule-associated protein (MAP) 1B accelerates apoptosis of cultured cortical neurons. J Biol Chem. 2003;278:366-371. https://doi.org/10.1074/jbc.M210091200
  31. Shah RD, Anderson KL, Rapoport M, Ferreira A. Estrogen-induced changes in the microtubular system correlate with a decreased susceptibility of aging neurons to beta amyloid neurotoxicity. Mol Cell Neurosci. 2003;24:503-516. https://doi.org/10.1016/S1044-7431(03)00166-0
  32. Lee ST, Han HJ, Oh SJ, Lee EJ, Han JY, Lim JM. Influence of ovarian hyperstimulation and ovulation induction on the cytoskeletal dynamics and developmental competence of oocytes. Mol Reprod Dev. 2006;73:1022-1033. https://doi.org/10.1002/mrd.20500
  33. Tanner SL, Franzen R, Jaffe H, Quarles RH. Evidence for expression of some microtubule-associated protein 1B in neurons as a plasma membrane glycoprotein. J Neurochem. 2000;75:553-562.
  34. Way AL. Isolation and culture of bovine oviductal epithelial cells for use in the anatomy and physiology laboratory and undergraduate research. Adv Physiol Educ. 2006;30:237-241. https://doi.org/10.1152/advan.00064.2005

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