Histone and N-terminal acetyltransferases play important roles in female reproduction and embryogenesis of the red flour beetle Tribolium castaneum.

IF 2.3 2区 农林科学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Karthi Sengodan, Subba Reddy Palli
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引用次数: 0

Abstract

Histone acetyltransferases (HATs) catalyse the addition of acetyl groups to histones and other proteins. In contrast, histone deacetylases remove acetyl groups from core histones, and the activity of these enzymes maintains the acetylation levels of these proteins. Histone acetylation levels influence chromatin accessibility and gene expression and regulate many biological processes, including development and reproduction. Recent reports suggest that some N-terminal acetyltransferases (NATs) also regulate gene expression. We identified 29 HAT and NAT genes in the red flour beetle, Tribolium castaneum, and studied their functions in female reproduction using RNA interference (RNAi). Knockdown of seven out of 13 HAT genes (N-acetyltransferase ESCO2) (ESCO1/2), Elongator complex protein 3 (ELP3), Histone acetyltransferase type B catalytic subunit 1 (HAT1), Transcription initiation factor TFIID subunit 1 (TAF1), Protein x-mas-2 (MCM3AP), Histone acetyltransferase Tip60 (KAT5), and Cysteine-rich protein 2-binding protein (KAT14) and 12 out of 16 NAT genes Probable glucosamine 6-phosphate N-acetyltransferase (GNPNAT1), N-alpha-acetyltransferase 10 (NAA10), N-alpha-acetyltransferase 20 (NAA20), N-alpha-acetyltransferase 30 (NAA30), N-alpha-acetyltransferase 40 (NAA40), N-alpha-acetyltransferase 60 (NAA60), N-acetyltransferase 6 (NAA80), RNA cytidine acetyltransferase (NAT10), Diamine acetyltransferase 2 (SATL1), N(alpha)-acetyltransferase 16 (NAA16), Phagocyte signalling-impaired protein (NAA25), N(alpha)-acetyltransferase 35 (NAA35) caused a significant reduction in eggs laid by females compared to the eggs laid by control females injected with dsGFP. Also, knockdown of nine (KAT5, ATAT1, ELP3, HAT1, KAT8A, NAA10, NAA20, GNPNAT1 and TAF1) HAT/NAT genes caused a significant decrease in egg hatching. Parental RNAi of ATAT1 and KAT8 blocked embryogenesis. These data suggest that the acetylation of proteins plays an important role in female reproduction and embryogenesis.

组蛋白和n端乙酰转移酶在红粉甲虫雌性生殖和胚胎发生中起重要作用。
组蛋白乙酰转移酶(HATs)催化在组蛋白和其他蛋白质上添加乙酰基。相反,组蛋白去乙酰化酶从核心组蛋白中去除乙酰基,这些酶的活性维持这些蛋白质的乙酰化水平。组蛋白乙酰化水平影响染色质可及性和基因表达,并调节许多生物过程,包括发育和生殖。最近的报道表明,一些n端乙酰转移酶(NATs)也调节基因表达。本研究从红粉甲虫(Tribolium castaneum)中鉴定出29个HAT和NAT基因,并利用RNA干扰(RNAi)技术研究了它们在雌性生殖中的功能。13个HAT基因中的7个基因(n -乙酰基转移酶ESCO2 (ESCO1/2)、延长体复合体蛋白3 (ELP3)、组蛋白乙酰基转移酶B型催化亚基1 (HAT1)、转录起始因子TFIID亚基1 (TAF1)、蛋白x- mas2 (MCM3AP)、组蛋白乙酰基转移酶Tip60 (KAT5)和富含半胱氨酸的蛋白2结合蛋白(KAT14))和16个NAT基因中的12个基因(可能的葡萄糖胺6-磷酸n -乙酰基转移酶(GNPNAT1)、n - α -乙酰基转移酶10 (NAA10))的敲低。N- α -乙酰转移酶20 (NAA20)、N- α -乙酰转移酶30 (NAA30)、N- α -乙酰转移酶40 (NAA40)、N- α -乙酰转移酶60 (NAA60)、N-乙酰转移酶6 (NAA80)、RNA胞苷乙酰转移酶(NAT10)、二胺乙酰转移酶2 (SATL1)、N(α)-乙酰转移酶16 (NAA16)、吞噬细胞信号传导受损蛋白(NAA25)、N(α)-乙酰转移酶35 (NAA35)使雌性产卵量显著减少,而对照雌性则注射了dsGFP。9个(KAT5、ATAT1、ELP3、HAT1、KAT8A、NAA10、NAA20、GNPNAT1和TAF1) HAT/NAT基因的敲低导致蛋孵化率显著降低。ATAT1和KAT8亲本RNAi阻断胚胎发生。这些数据表明,蛋白质的乙酰化在雌性生殖和胚胎发生中起着重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Insect Molecular Biology
Insect Molecular Biology 生物-昆虫学
CiteScore
4.80
自引率
3.80%
发文量
68
审稿时长
6-12 weeks
期刊介绍: Insect Molecular Biology has been dedicated to providing researchers with the opportunity to publish high quality original research on topics broadly related to insect molecular biology since 1992. IMB is particularly interested in publishing research in insect genomics/genes and proteomics/proteins. This includes research related to: • insect gene structure • control of gene expression • localisation and function/activity of proteins • interactions of proteins and ligands/substrates • effect of mutations on gene/protein function • evolution of insect genes/genomes, especially where principles relevant to insects in general are established • molecular population genetics where data are used to identify genes (or regions of genomes) involved in specific adaptations • gene mapping using molecular tools • molecular interactions of insects with microorganisms including Wolbachia, symbionts and viruses or other pathogens transmitted by insects Papers can include large data sets e.g.from micro-array or proteomic experiments or analyses of genome sequences done in silico (subject to the data being placed in the context of hypothesis testing).
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