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Abstract
Simple SummaryIndividuals with hermaphroditism are a serious hazard to animal husbandry and production due to their abnormal fertility. The molecular mechanism of sheep intersex formation was unclear. This study was the first to locate the homologous sequence of the goat polled intersex syndrome (PIS) region in sheep and found that the intersex traits of Lanzhou fat-tailed sheep were not caused by the lack of this region. By detecting the selective sweep regions, vital genes associated with androgen biosynthesis and the follicle stimulating hormone response entry were found, including steroid 5 alpha-reductase 2 (SRD5A2), and pro-apoptotic WT1 regulator (PAWR). Additionally, the copy number variations of the four regions on chr9, chr1, chr4, and chr16 may affect the expression of the gonadal development genes, zinc finger protein, FOG family member 2 (ZFPM2), LIM homeobox 8 (LHX8), inner mitochondrial membrane peptidase subunit 2 (IMMP2L) and slit guidance ligand 3 (SLIT3), respectively, and further affect the formation of intersex traits.Intersex, also known as hermaphroditism, is a serious hazard to animal husbandry and production. The mechanism of ovine intersex formation is not clear. Therefore, genome-wide resequencing on the only two intersex and two normal Lanzhou fat-tailed (LFT) sheep, an excellent but endangered Chinese indigenous sheep breed, was performed. Herein, the deletion of homologous sequences of the goat polled intersex syndrome (PIS) region (8787 bp, 247747059–247755846) on chromosome 1 of the LFT sheep was not the cause of the ovine intersex trait. By detecting the selective sweep regions, we found that the genes related to androgen biosynthesis and follicle stimulating hormone response items, such as steroid 5 alpha-reductase 2 (SRD5A2), steroid 5 alpha-reductase 3 (SRD5A3), and pro-apoptotic WT1 regulator (PAWR), may be involved in the formation of intersex traits. Furthermore, the copy number variations of the four regions, chr9: 71660801–71662800, chr1: 50776001–50778000, chr4: 58119201–58121600, and chr16: 778801–780800, may affect the expression of the zinc finger protein, FOG family member 2 (ZFPM2), LIM homeobox 8 (LHX8), inner mitochondrial membrane peptidase subunit 2 (IMMP2L) and slit guidance ligand 3 (SLIT3) genes, respectively, which contribute to the appearance of intersex traits. These results may supply a theoretical basis for the timely detection and elimination of intersex individuals in sheep, which could accelerate the healthy development of animal husbandry.
Highlights
Intersexuality, known as hermaphroditism, refers to the phenomenon that a dioecious animal is characterized by female-to-male sex reversal or abnormal gonad development
The deletion of the polled intersex syndrome (PIS) region was identified affecting the development of germ cell support cells, and it can affect the expression of genes, including Forkhead box L2 (FOXL2), PIS-regulated transcript 1 (PISRT1), and promoter FOXL2 inverse complementary (PFOXic) [6], indicating that the lack of the PIS region is closely related to goat intersex traits
The results show that most pathways, and gonadotropin response processes, such as UFM1 specific ligase 1 (UFL1), GTP-binding chromosomes contained windows with a higher differentiation coefficient, and chromosomes 2, 6, nuclear protein Ran-like (LOC105609617), mediator complex subunit 14 (MED14), DEAD-box helicase 5
Summary
Intersexuality, known as hermaphroditism, refers to the phenomenon that a dioecious animal is characterized by female-to-male sex reversal or abnormal gonad development. Intersex mostly occurs in the goat population, with high occurrence frequencies (about 3%–10%) [2], while related reports on horses, donkeys, pigs, and sheep are few. In goats, it is named polled intersex syndrome (PIS) for the phenomenon of intersex individuals often found in hornless goat populations [2]. The deletion of the PIS region was identified affecting the development of germ cell support cells, and it can affect the expression of genes, including Forkhead box L2 (FOXL2), PIS-regulated transcript 1 (PISRT1), and promoter FOXL2 inverse complementary (PFOXic) [6], indicating that the lack of the PIS region is closely related to goat intersex traits
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