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通过netrin轴突导向基因控制雄性和雌性生育能力。

Control of male and female fertility by the netrin axon guidance genes.

作者信息

Newquist Gunnar, Hogan Jesse, Walker Kirsti, Lamanuzzi Matthew, Bowser Micah, Kidd Thomas

机构信息

Department of Biology, University of Nevada, Reno, Nevada, United States of America.

出版信息

PLoS One. 2013 Aug 15;8(8):e72524. doi: 10.1371/journal.pone.0072524. eCollection 2013.

DOI:10.1371/journal.pone.0072524
PMID:23977313
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3744485/
Abstract

The netrin axon guidance genes have previously been implicated in fertility in C. elegans and in vertebrates. Here we show that adult Drosophila lacking both netrin genes, NetA and NetB, have fertility defects in both sexes together with an inability to fly and reduced viability. NetAB females produce fertilized eggs at a much lower rate than wild type. Oocyte development and ovarian innervation are unaffected in NetAB females, and the reproductive tract appears normal. A small gene, hog, that resides in an intron of NetB does not contribute to the NetAB phenotype. Restoring endogenous NetB expression rescues egg-laying, but additional genetic manipulations, such as restoration of netrin midline expression and inhibition of cell death have no effect on fertility. NetAB males induce reduced egg-laying in wild type females and display mirror movements of their wings during courtship. Measurement of courtship parameters revealed no difference compared to wild type males. Transgenic manipulations failed to rescue male fertility and mirror movements. Additional genetic manipulations, such as removal of the enabled gene, a known suppressor of the NetAB embryonic CNS phenotype, did not improve the behavioral defects. The ability to fly was rescued by inhibition of neuronal cell death and pan-neural NetA expression. Based on our results we hypothesize that the adult fertility defects of NetAB mutants are due to ovulation defects in females and a failure to properly transfer sperm proteins in males, and are likely to involve multiple neural circuits.

摘要

以往研究表明,线虫和脊椎动物中的netrin轴突导向基因与生育能力有关。在此我们发现,成年果蝇若同时缺失netrin基因NetA和NetB,雌雄两性都会出现生育缺陷,同时无法飞行且活力降低。NetAB雌性果蝇产生受精卵的速率远低于野生型。NetAB雌性果蝇的卵母细胞发育和卵巢神经支配未受影响,生殖道看起来也正常。位于NetB内含子中的一个小基因hog对NetAB表型没有影响。恢复内源性NetB表达可挽救产卵能力,但其他基因操作,如恢复netrin中线表达和抑制细胞死亡,对生育能力没有影响。NetAB雄性果蝇会使野生型雌性果蝇的产卵量减少,并且在求偶过程中翅膀会出现镜像运动。求偶参数测量结果显示,与野生型雄性果蝇相比没有差异。转基因操作未能挽救雄性果蝇的生育能力和镜像运动。其他基因操作,如去除已知的NetAB胚胎中枢神经系统表型抑制基因enabled,也未能改善行为缺陷。通过抑制神经元细胞死亡和泛神经NetA表达可挽救飞行能力。基于我们的研究结果,我们推测NetAB突变体的成年生育缺陷是由于雌性果蝇排卵缺陷和雄性果蝇未能正确转运精子蛋白,并且可能涉及多个神经回路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47d2/3744485/a44344a7f68f/pone.0072524.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47d2/3744485/f21c733e36f4/pone.0072524.g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47d2/3744485/f21c733e36f4/pone.0072524.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47d2/3744485/e8d982dd7028/pone.0072524.g002.jpg
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DCC expression by neurons regulates synaptic plasticity in the adult brain.神经元的 DCC 表达调控成年大脑中的突触可塑性。
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