Molecular Characteristics and Expression Analysis of amhr2 Gene in Bastard Halibut Paralichthys olivaceus
ZHANG Fayang1, LI Kun1, WANG Weichao1, ZHANG Dandan1, FU Xiaona1, LIU Cui1, ZHANG Junling1,2,3
1. Key Laboratory of Exploration and Utilization of Aquatic Germplasm Resources, Ministry of Education, Shanghai Ocean University, Shanghai 201306, China; 2. Aquatic Animal Genetic Breeding Center Shanghai Collaborative Innovation Center, Shanghai Ocean University, Shanghai 201306, China; 3. International Research Center for Marine Biosciences, Shanghai Ocean University, Shanghai 201306, China
Abstract:In order to investigate the molecular characteristics of anti-Müllerian hormone (AMH) and its type Ⅱ receptor AMHR2 and its role in gonadal development, the amhr2 gene was cloned in bastard halibut Paralichthys olivaceus with gonads from stage Ⅲ to stage Ⅳ and body weight of (720±50) g and identified by molecular cloning and bioinformatics methods. The expression profile of amhr2 gene was determined in gonad, brain, stomach, muscle, liver, kidney and heart of bastard halibut by semi-quantitative PCR and real-time fluorescence quantitative PCR and chemical in situ hybridization (ISH). The results showed that the amhr2 cDNA sequence obtained by cloning and splicing was 1536 bp in length and encoded 511 amino acids. The amino acid sequence analysis showed that the near N-terminus of the Amhr2 protein contained a signal peptide structure of 19 amino acids (1st—19th amino acids) and the amino acid sequence comparison showed that it had the maximal similarity with Hippoglossus stenolepis (89.96%). The evolutionary tree analysis revealed that the amhr2 gene of bastard halibut was the most closely related to H. stenolepis and turbot Scophthalmus maximus, and its evolutionary status was consistent, indicating that the amhr2 gene of bastard halibut is conserved with other species. The quantitative results showed that the amhr2 gene was mainly expressed in the ovaries and testes, with significantly higher expression level in the ovaries than that in the testes. The in situ hybridization results showed that amhr2 gene was mainly expressed in the sertoli cells, primary spermatocytes and secondary spermatocytes of the testis, and expressed in the interstitial cells, Ⅱ—Ⅴ oocytes and follicular membrane in the ovary. The amhr2 gene is most closely related to the H. stenolepis and expressed primarily in gonad and in both germ cells and somatic cells of the testis and ovary, which may be important for the regulation of gonadal development in the bastard halibut.
[1] PIEK E, HELDIN C H, TEN DIJKE P. Specificity, diversity, and regulation in TGF-beta superfamily signaling[J]. FASEB Journal:Official Publication of the Federation of American Societies for Experimental Biology,1999,13(15):2105-2124. [2] MULLEN R D, ONTIVEROS A E, MOSES M M, et al. AMH and AMHR2 mutations:a spectrum of reproductive phenotypes across vertebrate species[J]. Developmental Biology,2019,455(1):1-9. [3] JOSSO N. Anti-Müllerian hormone[J]. Baillière's Clinical Endocrinology and Metabolism,1991,5(4):635-654. [4] BEHRINGER R R, FINEGOLD M J, CATE R L. Müllerian-inhibiting substance function during mammalian sexual development[J]. Cell,1994,79(3):415-425. [5] DEWAILLY D, ANDERSEN C Y, BALEN A, et al. The physiology and clinical utility of anti-Müllerian hormone in women[J]. Human Reproduction Update,2014,20(3):370-385. [6] LEE M M, SEAH C C, MASIAKOS P T, et al. Müllerian-inhibiting substance type Ⅱ receptor expression and function in purified rat Leydig cells[J]. Endocrinology,1999,140(6):2819-2827. [7] RACINE C, REY R, FOREST M G, et al. Receptors for anti-Müllerian hormone on Leydig cells are responsible for its effects on steroidogenesis and cell differentiation[J]. Proceedings of the National Academy of Sciences of the United States of America,1998,95(2):594-599. [8] BAARENDS W M, HOOGERBRUGGE J W, POST M, et al. Anti-Müllerian hormone and anti-Müllerian hormone type Ⅱ receptor messenger ribonucleic acid expression during postnatal testis development and in the adult testis of the rat[J]. Endocrinology,1995,136(12):5614-5622. [9] BAARENDS W M, UILENBROEK J T, KRAMER P, et al. Anti-Müllerian hormone and anti-Müllerian hormone type Ⅱ receptor messenger ribonucleic acid expression in rat ovaries during postnatal development, the estrous cycle, and gonadotropin-induced follicle growth[J]. Endocrinology,1995,136(11):4951-4962. [10] DI CLEMENTE N, WILSON C, FAURE E, et al. Cloning, expression, and alternative splicing of the receptor for anti-Müllerian hormone[J]. Molecular Endocrinology,1994,8(8):1006-1020. [11] HU Q, GUO W, GAO Y, et al. Molecular cloning and characterization of amh and Dax1 genes and their expression during sex inversion in rice-field eel Monopterus albus[J]. Scientific Reports,2015,5:16667. [12] LI M, WANG L H, WANG H P, et al. Molecular cloning and characterization of amh, dax1 and cyp19a1a genes and their response to 17α-methyltestosterone in Pengze crucian carp[J]. Comparative Biochemistry and Physiology Part C:Toxicology & Pharmacology,2013,157(4):372-381. [13] POONLAPHDECHA S, PEPEY E, HUANG S H, et al. Elevated amh gene expression in the brain of male Tilapia (Oreochromis niloticus) during testis differentiation[J]. Sexual Development,2011,5(1):33-47. [14] OLIVEIRA M A, MARTINEZ E R M, BUTZGE A J, et al. Molecular characterization and expression analysis of anti-Müllerian hormone in common carp (Cyprinus carpio) adult testes[J]. Gene Expression Patterns,2021,40:119169. [15] HAN Y L, ZHAO M, WANG L, et al. Overexpression of anti-Müllerian hormone gene in vivo affects gonad sex differentiation in undifferentiated orange-spotted groupers (Epinephelus coioides)[J]. Frontiers in Endocrinology,2019,10:210. [16] KAMIYA T, KAI W, TASUMI S, et al. A trans-species missense SNP in Amhr2 is associated with sex determination in the tiger pufferfish, Takifugu rubripes (fugu)[J]. PLoS Genetics,2012,8(7):e1002798. [17] LI M H, SUN Y L, ZHAO J E, et al. A tandem duplicate of anti-Müllerian hormone with a missense SNP on the Y chromosome is essential for male sex determination in Nile tilapia, Oreochromis niloticus[J]. PLoS Genetics,2015,11(11):e1005678. [18] LIN Q H, MEI J E, LI Z, et al. Distinct and cooperative roles of amh and dmrt1 in self-renewal and differentiation of male germ cells in zebrafish[J]. Genetics,2017,207(3):1007-1022. [19] LIU X Y, XIAO H S, JIE M M, et al. Amh regulate female folliculogenesis and fertility in a dose-dependent manner through Amhr2 in Nile tilapia[J]. Molecular and Cellular Endocrinology,2020,499:110593. [20] PAN Q W, FERON R, YANO A, et al. Identification of the master sex determining gene in northern pike (Esox lucius) reveals restricted sex chromosome differentiation[J]. PLoS Genetics,2019,15(8):e1008013. [21] 陈晶,吴立新,吴玉波,等.不同摄食水平对牙鲆幼鱼生长及能量收支的影响[J].水产科学,2012,31(1):1-6. [22] YOSHINAGA N, SHIRAISHI E, YAMAMOTO T, et al. Sexually dimorphic expression of a teleost homologue of Müllerian inhibiting substance during gonadal sex differentiation in Japanese flounder, Paralichthys olivaceus[J]. Biochemical and Biophysical Research Communications,2004,322(2):508-513. [23] FAN Z F, ZOU Y X, LIANG D D, et al. Roles of forkhead box protein L2 (foxl2) during gonad differentiation and maintenance in a fish, the olive flounder (Paralichthys olivaceus)[J]. Reproduction, Fertility and Development,2019,31(11):1742. [24] 王学颖.牙鲆原始生殖细胞的起源、增殖和迁移以及高温雄性化的机制研究[D].青岛:中国科学院研究生院(海洋研究所),2015. [25] WANG W X, LIANG S S, ZOU Y X, et al. Amh dominant expression in Sertoli cells during the testicular differentiation and development stages in the olive flounder Paralichthys olivaceus[J]. Gene,2020,755:144906. [26] 申峰峰,晁青何,黄沁怡,等. miR-202-5p在牙鲆性腺中的表达分析及其与cbx2靶向关系验证[J].水生生物学报,2021,45(4):741-748. [27] VISSER J A, THEMMEN A P N. Role of anti-Müllerian hormone and bone morphogenetic proteins in the regulation of FSH sensitivity[J]. Molecular and Cellular Endocrinology, 2014,382(1):460-465. [28] JAMIN S P, ARANGO N A, MISHINA Y, et al. Genetic studies of the AMH/MIS signaling pathway for Müllerian duct regression[J]. Molecular and Cellular Endocrinology,2003,211(1/2):15-19. [29] 王妹,邓思平,陈华谱,等.金钱鱼Amhr2基因的克隆及表达分析[J].广东海洋大学学报,2018,38(3):17-24. [30] KLÜVER N, PFENNIG F, PALA I, et al. Differential expression of anti-Müllerian hormone (amh) and anti-Müllerian hormone receptor type Ⅱ (amhrⅡ) in the teleost medaka[J]. Developmental Dynamics,2007,236(1):271-281. [31] 高莹莹,胡鹏,刘新富,等.暗纹东方鲀抗苗勒氏管激素Ⅱ型受体基因的克隆、生物信息学及表达分析[J].海洋渔业,2019,41(5):555-566. [32] 高长富,郝薇薇,仇雪梅,等.红鳍东方鲀抗苗勒氏管激素(AMH)基因在不同发育时期的组织表达[J].大连海洋大学学报,2016,31(4):390-396. [33] 姜洁明,沈旭芳,刘鹰,等.红鳍东方鲀幼鱼中性别分化相关基因的表达分析[J].水产科学,2022,41(3):362-369. [34] MIURA T, MIURA C, KONDA Y, et al. Spermatogenesis-preventing substance in Japanese eel[J]. Development,2002,129(11):2689-2697. [35] 李兵部,曹哲明,陶易凡,等.大口黑鲈amh基因全长cDNA克隆、表达及多克隆抗体制备[J].水生生物学报,2023,47(5):775-785. [36] SHIRAISHI E, YOSHINAGA N, MIURA T, et al. Mullerian inhibiting substance is required for germ cell proliferation during early gonadal differentiation in medaka (Oryzias latipes)[J]. Endocrinology,2008,149(4):1813-1819. [37] WU G C, CHIU P C, LYU Y S, et al. The expression of amh and amhr2 is associated with the development of gonadal tissue and sex change in the protandrous black porgy, Acanthopagrus schlegeli[J]. Biology of Reproduction,2010,83(3):443-453. [38] RAYMOND C S, MURPHY M W, O'SULLIVAN M G, et al. Dmrt1, a gene related to worm and fly sexual regulators, is required for mammalian testis differentiation[J]. Genes & Development,2000,14(20):2587-2595. [39] BAARENDS W, VAN HELMOND M, POST M, et al. A novel member of the transmembrane serine/threonine kinase receptor family is specifically expressed in the gonads and in mesenchymal cells adjacent to the Mullerian duct[J]. Development,1994,120(1):189. [40] RENAUD E J, MACLAUGHLIN D T, OLIVA E, et al. Endometrial cancer is a receptor-mediated target for Mullerian Inhibiting Substance[J]. Proceedings of the National Academy of Sciences of the United States of America,2005,102(1):111-116. [41] HOSHIYA Y, GUPTA V, SEGEV D L, et al. Mullerian Inhibiting Substance induces NFkB signaling in breast and prostate cancer cells[J]. Molecular and Cellular Endocrinology,2003,211(1/2):43-49. [42] JOSSO N, RACINE C, DI CLEMENTE N, et al. The role of anti-Müllerian hormone in gonadal development[J]. Molecular and Cellular Endocrinology,1998,145(1/2):3-7. [43] MISHINA Y, WHITWORTH D J, RACINE C, et al. High specificity of Müllerian-inhibiting substance signaling in vivo[J]. Endocrinology,1999,140(5):2084-2088. [44] LUI P Y, JIN D Y, STEVENSON N J. MicroRNA:master controllers of intracellular signaling pathways[J]. Cellular and Molecular Life Sciences,2015,72(18):3531-3542. [45] HATA A, CHEN Y G. TGF-β signaling from receptors to smads[J]. Cold Spring Harbor Perspectives in Biology,2016,8(9):a022061. [46] 亢逸,关桂君,洪云汉.用模式生物青鳉概观硬骨鱼性别决定及性分化研究进展[J].遗传,2017,39(6):441-454. [47] 柳兴永.Amh/Amhy在罗非鱼生殖中的功能研究与可育YY伪雌鱼的培育[D].重庆:西南大学,2020. [48] FERON R, ZAHM M, CABAU C, et al. Characterization of a Y-specific duplication/insertion of the anti-Mullerian hormone type Ⅱ receptor gene based on a chromosome-scale genome assembly of yellow perch, Perca flavescens[J]. Molecular Ecology Resources,2020,20(2):531-543.