Abstract

Background: Polled intersex syndrome (PIS) leads to reproductive disorders in goats and exerts a heavy influence on goat breeding. Since 2001, the core variant of an 11.7 kb deletion at ~129 Mb on chromosome 1 (CHI1) has been widely used as a genetic diagnostic criterion. In 2020, a ~0.48 Mb insertion within the PIS deletion was identified by sequencing in XX intersex goats. However, the suitability of this variation for the diagnosis of intersex goats worldwide and its further molecular genetic mechanism need to be clarified.Results: The whole-genome selective sweep of intersex goats from China was performed with whole-genome next-generation sequencing technology for large sample populations and a case–control study on interbreeds. A series of candidate genes related to the goat intersexuality phenotype were found. We further confirmed that a ~0.48 Mb duplicated fragment (including ERG and KCNJ15) downstream of the ~20 Mb PIS region was reversely inserted into the PIS locus in intersex Chinese goats and was consistent with that in European Saanen and Valais black-necked goats. High-throughput chromosome conformation capture (Hi-C) technology was then used to compare the 3D structures of the PIS variant neighborhood in CHI1 between intersex and non-intersex goats. A newly found structure was validated as an intrachromosomal rearrangement. This inserted duplication changed the original spatial structure of goat CHI1 and caused the appearance of several specific loop structures in the adjacent ~20 kb downstream region of FOXL2.Conclusions: Results suggested that the novel complex PIS variant genome was sufficient as a broad-spectrum clinical diagnostic marker of XX intersexuality in goats from Europe and China. A series of private dense loop structures caused by segment insertion into the PIS deletion might affect the expression of FOXL2 or other neighboring novel candidate genes. However, these structures require further in-depth molecular biological experimental verification. In general, this study provided new insights for future research on the molecular genetic mechanism underlying female-to-male sex reversal in goats.

Highlights

  • Polled intersex syndrome (PIS) leads to reproductive disorders in goats and exerts a heavy influence on goat breeding

  • A total of 16 462,769 Single nucleotide polymorphism (SNP) and 1,058 Copy number variant (CNV) were obtained from 221 samples

  • The results revealed that 50 windows were generated by the intersection of the top 1% selective regions of the Pairwise fixation index (FST) and π ratios and 79 genes, which covered or were located up- and downstream within the 300 kb range of the window

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Summary

Introduction

Polled intersex syndrome (PIS) leads to reproductive disorders in goats and exerts a heavy influence on goat breeding. In 2020, a ∼0.48 Mb insertion within the PIS deletion was identified by sequencing in XX intersex goats. During breeding, the proportion of intersex individuals in the hornless goat population gradually increased. This phenomenon was termed polled intersex syndrome (PIS) (Eaton, 1945). Intersexuality, the phenomenon wherein certain dioecious organisms possess both sexes, has been widely observed in various livestock species (Bosu and Basrur, 1984; Wang and Zhang, 1993), including goats (Ramadan and El Hassan, 1988; Ramadan et al, 1991), within the last century. Reproductive system malformations in PIS goats lead to the loss of reproductive capacity and are some of the great challenges encountered in the development of the goat industry

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