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人类14-3-3ζ假基因的结构特征与生理关联

Structural Features and Physiological Associations of Human 14-3-3ζ Pseudogenes.

作者信息

Lughmani Haroon, Patel Hrushil, Chakravarti Ritu

机构信息

Department of Physiology and Pharmacology, The University of Toledo, Toledo, OH 43614, USA.

出版信息

Genes (Basel). 2024 Mar 24;15(4):399. doi: 10.3390/genes15040399.

DOI:10.3390/genes15040399
PMID:38674334
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11049341/
Abstract

There are about 14,000 pseudogenes that are mutated or truncated sequences resembling functional parent genes. About two-thirds of pseudogenes are processed, while others are duplicated. Although initially thought dead, emerging studies indicate they have functional and regulatory roles. We study 14-3-3ζ, an adaptor protein that regulates cytokine signaling and inflammatory diseases, including rheumatoid arthritis, cancer, and neurological disorders. To understand how 14-3-3ζ (gene symbol YWHAZ) performs diverse functions, we examined the human genome and identified nine YWHAZ pseudogenes spread across many chromosomes. Unlike the 32 kb exon-to-exon sequence in YWHAZ, all pseudogenes are much shorter and lack introns. Out of six, four YWHAZ exons are highly conserved, but the untranslated region (UTR) shows significant diversity. The putative amino acid sequence of pseudogenes is 78-97% homologous, resulting in striking structural similarities with the parent protein. The OMIM and Decipher database searches revealed chromosomal loci containing pseudogenes are associated with human diseases that overlap with the parent gene. To the best of our knowledge, this is the first report on pseudogenes of the 14-3-3 family protein and their implications for human health. This bioinformatics-based study introduces a new insight into the complexity of 14-3-3ζ's functions in biology.

摘要

大约有14000个假基因,它们是与功能正常的亲本基因相似的突变或截短序列。大约三分之二的假基因是经过加工的,而其他的则是复制产生的。尽管最初被认为是无功能的,但新出现的研究表明它们具有功能和调控作用。我们研究了14-3-3ζ,一种调节细胞因子信号传导和炎症性疾病(包括类风湿性关节炎、癌症和神经疾病)的衔接蛋白。为了了解14-3-3ζ(基因符号YWHAZ)如何发挥多种功能,我们检测了人类基因组并鉴定出九个分布在多条染色体上的YWHAZ假基因。与YWHAZ中32kb的外显子到外显子序列不同,所有假基因都短得多且缺乏内含子。在六个YWHAZ外显子中,有四个高度保守,但非翻译区(UTR)显示出显著的多样性。假基因的推定氨基酸序列同源性为78-97%,与亲本蛋白在结构上有显著相似性。对OMIM和Decipher数据库的搜索显示,含有假基因的染色体位点与与亲本基因重叠的人类疾病有关。据我们所知,这是关于14-3-3家族蛋白假基因及其对人类健康影响的首次报道。这项基于生物信息学的研究为14-3-3ζ在生物学中的功能复杂性引入了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd7/11049341/4104f45299b9/genes-15-00399-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd7/11049341/d9d378aa8542/genes-15-00399-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd7/11049341/1fc8a11e71e3/genes-15-00399-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd7/11049341/e4cedc08665c/genes-15-00399-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd7/11049341/801005b75210/genes-15-00399-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd7/11049341/4104f45299b9/genes-15-00399-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd7/11049341/d9d378aa8542/genes-15-00399-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd7/11049341/1fc8a11e71e3/genes-15-00399-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd7/11049341/e4cedc08665c/genes-15-00399-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd7/11049341/801005b75210/genes-15-00399-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd7/11049341/4104f45299b9/genes-15-00399-g005.jpg

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J Immunol Res. 2022 Sep 28;2022:5633096. doi: 10.1155/2022/5633096. eCollection 2022.
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YWHAZ variation causes intellectual disability and global developmental delay with brain malformation.YWHAZ 变异导致伴脑畸形的智力残疾和全面发育迟缓。
Hum Mol Genet. 2023 Jan 13;32(3):462-472. doi: 10.1093/hmg/ddac210.
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