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UBR4 deficiency causes male sterility and testis abnormal in Drosophila

INTRODUCTION: It has been established that UBR4 encodes E3 ubiquitin ligase, which determines the specificity of substrate binding during protein ubiquitination and has been associated with various functions of the nervous system but not the reproductive system. Herein, we explored the role of UBR4...

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Autores principales: Xie, Shi-Ming, Lai, Jia-Xuan, Liu, Chu-Qiao, Zhang, Xi-Xing, Lin, Yong-Miao, Lan, Qi-Wen, Hong, De-Yao, Chen, Xiao-Chuan, Qiao, Jing-Da, Mao, Yu-Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10390308/
https://www.ncbi.nlm.nih.gov/pubmed/37529615
http://dx.doi.org/10.3389/fendo.2023.1165825
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author Xie, Shi-Ming
Lai, Jia-Xuan
Liu, Chu-Qiao
Zhang, Xi-Xing
Lin, Yong-Miao
Lan, Qi-Wen
Hong, De-Yao
Chen, Xiao-Chuan
Qiao, Jing-Da
Mao, Yu-Ling
author_facet Xie, Shi-Ming
Lai, Jia-Xuan
Liu, Chu-Qiao
Zhang, Xi-Xing
Lin, Yong-Miao
Lan, Qi-Wen
Hong, De-Yao
Chen, Xiao-Chuan
Qiao, Jing-Da
Mao, Yu-Ling
author_sort Xie, Shi-Ming
collection PubMed
description INTRODUCTION: It has been established that UBR4 encodes E3 ubiquitin ligase, which determines the specificity of substrate binding during protein ubiquitination and has been associated with various functions of the nervous system but not the reproductive system. Herein, we explored the role of UBR4 on fertility with a Drosophila model. METHODS: Different Ubr4 knockdown flies were established using the UAS/GAL4 activating sequence system. Fertility, hatchability, and testis morphology were studied, and bioinformatics analyses were conducted. Our results indicated that UBR4 deficiency could induce male sterility and influent egg hatchability in Drosophila. RESULTS: We found that Ubr4 deficiency affected the testis during morphological analysis. Proteomics analysis indicated 188 upregulated proteins and 175 downregulated proteins in the testis of Ubr4 knockdown flies. Gene Ontology analysis revealed significant upregulation of CG11598 and Sfp65A, and downregulation of Pelota in Ubr4 knockdown flies. These proteins were involved in the biometabolic or reproductive process in Drosophila. These regulated proteins are important in testis generation and sperm storage promotion. Bioinformatics analysis verified that UBR4 was low expressed in cryptorchidism patients, which further supported the important role of UBR4 in male fertility. DISCUSSION: Overall, our findings suggest that UBR4 deficiency could promote male infertility and may be involved in the protein modification of UBR4 by upregulating Sfp65A and CG11598, whereas downregulating Pelota protein expression.
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spelling pubmed-103903082023-08-01 UBR4 deficiency causes male sterility and testis abnormal in Drosophila Xie, Shi-Ming Lai, Jia-Xuan Liu, Chu-Qiao Zhang, Xi-Xing Lin, Yong-Miao Lan, Qi-Wen Hong, De-Yao Chen, Xiao-Chuan Qiao, Jing-Da Mao, Yu-Ling Front Endocrinol (Lausanne) Endocrinology INTRODUCTION: It has been established that UBR4 encodes E3 ubiquitin ligase, which determines the specificity of substrate binding during protein ubiquitination and has been associated with various functions of the nervous system but not the reproductive system. Herein, we explored the role of UBR4 on fertility with a Drosophila model. METHODS: Different Ubr4 knockdown flies were established using the UAS/GAL4 activating sequence system. Fertility, hatchability, and testis morphology were studied, and bioinformatics analyses were conducted. Our results indicated that UBR4 deficiency could induce male sterility and influent egg hatchability in Drosophila. RESULTS: We found that Ubr4 deficiency affected the testis during morphological analysis. Proteomics analysis indicated 188 upregulated proteins and 175 downregulated proteins in the testis of Ubr4 knockdown flies. Gene Ontology analysis revealed significant upregulation of CG11598 and Sfp65A, and downregulation of Pelota in Ubr4 knockdown flies. These proteins were involved in the biometabolic or reproductive process in Drosophila. These regulated proteins are important in testis generation and sperm storage promotion. Bioinformatics analysis verified that UBR4 was low expressed in cryptorchidism patients, which further supported the important role of UBR4 in male fertility. DISCUSSION: Overall, our findings suggest that UBR4 deficiency could promote male infertility and may be involved in the protein modification of UBR4 by upregulating Sfp65A and CG11598, whereas downregulating Pelota protein expression. Frontiers Media S.A. 2023-07-10 /pmc/articles/PMC10390308/ /pubmed/37529615 http://dx.doi.org/10.3389/fendo.2023.1165825 Text en Copyright © 2023 Xie, Lai, Liu, Zhang, Lin, Lan, Hong, Chen, Qiao and Mao https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Xie, Shi-Ming
Lai, Jia-Xuan
Liu, Chu-Qiao
Zhang, Xi-Xing
Lin, Yong-Miao
Lan, Qi-Wen
Hong, De-Yao
Chen, Xiao-Chuan
Qiao, Jing-Da
Mao, Yu-Ling
UBR4 deficiency causes male sterility and testis abnormal in Drosophila
title UBR4 deficiency causes male sterility and testis abnormal in Drosophila
title_full UBR4 deficiency causes male sterility and testis abnormal in Drosophila
title_fullStr UBR4 deficiency causes male sterility and testis abnormal in Drosophila
title_full_unstemmed UBR4 deficiency causes male sterility and testis abnormal in Drosophila
title_short UBR4 deficiency causes male sterility and testis abnormal in Drosophila
title_sort ubr4 deficiency causes male sterility and testis abnormal in drosophila
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10390308/
https://www.ncbi.nlm.nih.gov/pubmed/37529615
http://dx.doi.org/10.3389/fendo.2023.1165825
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