Molecular characterization and expression profiling of transformer 2 and fruitless- like homologs in the black tiger shrimp, Penaeus monodon

被引:4
|
作者
Thaijongrak, Prawporn [1 ,2 ,3 ]
Chotwiwatthanakun, Charoonroj [1 ,4 ]
Laphyai, Phaivit [1 ,2 ]
Prachumwat, Anuphap [1 ,5 ]
Kruangkum, Thanapong [1 ,2 ]
Sobhon, Prasert [2 ]
Vanichviriyakit, Rapeepun [1 ,2 ]
机构
[1] Mahidol Univ, Fac Sci, Ctr Excellence Shrimp Mol Biol & Biotechnol, Bangkok, Thailand
[2] Mahidol Univ, Fac Sci, Dept Anat, Bangkok, Thailand
[3] Mahidol Univ, Fac Vet Sci, Dept Clin Sci & Publ Hlth, Salaya, Nakhon Pathom, Thailand
[4] Mahidol Univ, Nakhonsawan Campus, Nakhonsawan, Thailand
[5] Natl Sci & Technol Dev Agcy, Natl Ctr Genet Engn & Biotechnol, Pathum Thani, Thailand
来源
PEERJ | 2022年 / 10卷
关键词
Sex determination; Crustacean; Shrimp; DROSOPHILA SEX-DETERMINATION; ANDROGENIC GLAND; DOUBLESEX GENE; MALE COURTSHIP; BEHAVIOR; BINDING; RNA; DIFFERENTIATION; IDENTIFICATION; MELANOGASTER;
D O I
10.7717/peerj.12980
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Transformer 2 (tra 2) and fruitless (fru) genes have been proven to play a key role in sex determination pathways in many Arthropods, including insects and crustaceans. In this study, a paralog of P. monodon tra 2 (Pmtra 2), P. monodon ovarian associated transformer 2 (PmOvtra 2) and 2 isoforms of P. monodon fruitless-like gene (Pmfru-1 and Pmfru-2) were identified and characterized. The full cDNA sequence of PmOvtra 2 consisted of 1,774 bp with the longest open reading frame (ORF) of 744 bp encoding for 247 amino acids. The PmOvtra 2 exhibited a predicted RNA-recognition motif (RRM) domain and two arginine-serine (RS) regions, suggesting its function in RNA splicing. The full cDNA sequence of Pmfru-1 consisted of 1,306 bp with 1,182 bp ORF encoding for 393 amino acids, whereas the full cDNA sequence of Pmfru-2 consisted of 1,858 bp with 1,437 bp ORF encoding 478 amino acids. The deduced amino acid sequences of Pmfru-1 and Pmfru-2 exhibited highly conserved domains of Fru proteins, including Broad-complex, Tramtrack and Bric-a-brac (BTB), and zinc finger (ZF) domains. In addition, Pmfru-1 and Pmfru-2 were suggestively originated from the same single genomic locus by genomic sequence analysis. Specifically, Pmfru pre-mRNA was alternatively spliced for Pmfru-1 and Pmfru-2 to include mutually exclusive exon 7 and exon 6, respectively. Temporal and spatial expression of PmOvtra 2, Pmfru-1, and Pmfru-2 were also investigated by qPCR. The results showed that all were expressed in early developmental stages with undifferentiated gonads starting from nauplius until postlarvae. The expression of PmOvtra 2 started at nauplius stage and gradually increased from mysis to postlarvae (PL) 1. However, the expression of Pmfru-1 was low at the nauplii stage and slightly increased from protozoea to PL5, whereas the expression of Pmfru-2 maintained a low level from nauplius to mysis and then gradually increased at the PL stages. Expressions of PmOvtra 2, Pmfru-1, and Pmfru-2 were detected in various tissues including nervous tissue, gill, heart, hepatopancreas, gut, and gonads. Interestingly, the sexually dimorphic expression of PmOvtra 2, Pmfru-1, and Pmfru-2 was demonstrated in fully developed gonads in which the ovary showed significantly higher expressions than the testis. The great difference in the expression pattern of PmOvtra 2, Pmfru-1, and Pmfru-2 in the ovary and testis suggested their roles in the female sex determination in P. monodon.
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页数:25
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