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KN 基序和 AnKyrin 重复结构域 1(KANK1)缺失导致小鼠模型中淋巴组织失调。

Loss of the KN Motif and AnKyrin Repeat Domain 1 (KANK1) Leads to Lymphoid Compartment Dysregulation in Murine Model.

机构信息

Department of Hematology, Rigshospitalet, 2100 Copenhagen, Denmark.

Biotech Research and Innovation Centre (BRIC), Faculty of Health and Medical Sciences, University of Copenhagen, 4072 Copenhagen, Denmark.

出版信息

Genes (Basel). 2023 Oct 16;14(10):1947. doi: 10.3390/genes14101947.

Abstract

The KN Motif and AnKyrin Repeat Domain 1 () is proposed as a tumour suppressor gene, as its expression is reduced or absent in several types of tumour tissue, and over-expressing the protein inhibited the proliferation of tumour cells in solid cancer models. We report a novel germline loss of heterozygosity mutation encompassing the gene in a young patient diagnosed with myelodysplastic neoplasm (MDS) with no additional disease-related genomic aberrations. To study the potential role of KANK1 in haematopoiesis, we generated a new transgenic mouse model with a confirmed loss of KANK1 expression. KANK1 knockout mice did not develop any haematological abnormalities; however, the loss of its expression led to alteration in the colony forming and proliferative potential of bone marrow (BM) cells and a decrease in hematopoietic stem and progenitor cells (HSPCs) population frequency. A comprehensive marker expression analysis of lineage cell populations indicated a role for in lymphoid cell development, and total protein analysis suggests the involvement of in BM cells' cytoskeleton formation and mobility.

摘要

KN 基序和 AnKyrin 重复结构域 1 () 被认为是一种肿瘤抑制基因,因为其在多种类型的肿瘤组织中表达减少或缺失,并且过表达该蛋白可抑制实体瘤模型中肿瘤细胞的增殖。我们报道了一例新的种系杂合性缺失突变,该突变涵盖了一个年轻 MDS 患者中的 基因,该患者没有其他与疾病相关的基因组异常。为了研究 KANK1 在造血中的潜在作用,我们生成了一种新型的转基因小鼠模型,该模型可证实 KANK1 的表达缺失。KANK1 敲除小鼠未出现任何血液学异常;然而,其表达的缺失导致骨髓 (BM) 细胞的集落形成和增殖潜力发生改变,以及造血干细胞和祖细胞 (HSPCs) 群体频率降低。对谱系细胞群体的全面标记表达分析表明 参与了淋巴细胞的发育,总蛋白分析表明 参与了 BM 细胞细胞骨架的形成和运动。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7930/10605996/0275040937ec/genes-14-01947-g001.jpg

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