罕见但特异:5-bp复合基序定义BMP信号中SMAD结合。

IF 4.5 1区 生物学 Q1 BIOLOGY BMC Biology Pub Date : 2025-03-13 DOI:10.1186/s12915-025-02183-1
Jerome Jatzlau, Sophie-Nhi Do, Rebeca A Mees, Paul-Lennard Mendez, Rameez Jabeer Khan, Lukas Maas, Lidia Ruiz, Pau Martin-Malpartida, Maria J Macias, Petra Knaus
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引用次数: 0

摘要

背景:受体激活的SMADs与SMAD4三聚体化以调节环境依赖性靶基因的表达。然而,单个SMAD1/5/8结合基序在顺式调控元件中的存在并不会在天然环境中触发转录。我们假设,结合至少两个SMAD结合位点非常接近的复合基序就足以诱导转录,因为这种情况允许至少两个SMAD蛋白同时相互作用,从而增加特异性和亲和力。结果:使用超过65种不同的萤火虫荧光素酶结构,我们描绘了bmp诱导基因激活的最低要求。我们提出了一个模型,其中两个SMAD-MH1结构域以背靠背的方式结合smad -复合基序,在相反的DNA链上smad -基序之间有5bp的距离。然而,对各种细胞类型的SMAD1结合区域的筛选表明,这些复合基元极为罕见,解释了不到1%的SMAD1结合事件。结论:偏离这些最低要求会阻碍转录,并强调需要共转录因子来实现基因激活。
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Rare but specific: 5-bp composite motifs define SMAD binding in BMP signaling.

Background: Receptor-activated SMADs trimerize with SMAD4 to regulate context-dependent target gene expression. However, the presence of a single SMAD1/5/8 binding motif in cis-regulatory elements alone does not trigger transcription in native contexts. We hypothesize that binding to composite motifs in which at least two SMAD binding sites are in close proximity would be enough to induce transcription as this scenario allows the simultaneous interaction of at least two SMAD proteins, thereby increasing specificity and affinity.

Results: Using more than 65 distinct firefly luciferase constructs, we delineated the minimal requirements for BMP-induced gene activation. We propose a model in which two SMAD-MH1 domains bind a SMAD-composite motif in a back-to-back fashion with a 5-bp distance between the SMAD-motifs on opposing DNA strands. However screening of SMAD1-bound regions across a variety of cell types highlights that these composite motifs are extremely uncommon, explaining below 1% of SMAD1 binding events.

Conclusions: Deviations from these minimal requirements prevent transcription and underline the need for co-transcription factors to achieve gene activation.

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来源期刊
BMC Biology
BMC Biology 生物-生物学
CiteScore
7.80
自引率
1.90%
发文量
260
审稿时长
3 months
期刊介绍: BMC Biology is a broad scope journal covering all areas of biology. Our content includes research articles, new methods and tools. BMC Biology also publishes reviews, Q&A, and commentaries.
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