ドロソフィラ Ubxとabd-Aタンパク質による遺伝子活性化とDNA結合
M L Samson1, L Jackson-Grusby, R Brent
1Department of Molecular Biology, Massachusetts General Hospital, Boston 02114.
Cell
|June 16, 1989
まとめ
Ubxとabd-Aタンパク質は,ドロソフィラの発達に不可欠である. 彼らのホメオドメインはDNAの結合に不可欠ですが,DNAの結合が他のタンパク質によって促進される場合,二分化,核への入り込み,または活性化には欠かせません.
科学分野:
- 発達生物学 発達生物学について
- 分子遺伝学 分子遺伝学
- ドロソフィラ・メラノガスターの研究
背景:
- Ubxとabd-A遺伝子の産物は,ドロソフィラの胸部と腹部構造の適切な発達に不可欠です.
- これらの転写因子の正確な分子機構を理解することは,発達経路の解読の鍵です.
研究 の 目的:
- Ubxおよびabd-Aタンパク質におけるホメオドメインのDNA結合と遺伝子活性化に関する機能的役割を調査する.
- Ubxとabd-A.によって媒介される二分化,核局所化,および転写調節に関する要件を解明する.
主な方法:
- 酵母におけるLexA-UbxとLexA-abdA融合タンパク質の発現.
- 遺伝子活性化を評価するために,LexAオペレーターまたはUbx結合部位を持つ標的遺伝子を利用する.
- ホメオドメインの機能を解剖するために,突然変異した融合タンパク質を使用します.
主要な成果:
- LexA-UbxとLexA-abdA融合タンパク質が標的遺伝子発現を活性化しました.
- ホメオドメインは,タンパク質の二重化や核の侵入に不可欠ではありませんでした.
- ホメオドメインは,DNA結合がLexA部分によって媒介されたとき,遺伝子の活性化には欠かせませんでした.
- ホメオドメインはUbxサイトに結合するために必要ですが,そのDNAの相互作用は,細菌のヘリックス-ターン-ヘリックスタンパク質とは異なります.
結論:
- ホメオドメインは,Ubxとabd-Aが特定のDNA部位に結合するのに不可欠です.
- Ubxとabd-Aによる遺伝子活性化は,主にDNA結合によって引き起こされます.
- これらのタンパク質によるネガティブな遺伝子調節は,おそらく他のドロソフィラの遺伝子産物との相互作用を含む.
関連する概念動画
RNA Polymerase II Accessory Proteins
8.9K
Proteins that regulate transcription can do so either via direct contact with RNA Polymerase or through indirect interactions facilitated by adaptors, mediators, histone-modifying proteins, and nucleosome remodelers. Direct interactions to activate transcription is seen in bacteria as well as in some eukaryotic genes. In these cases, upstream activation sequences are adjacent to the promoters, and the activator proteins interact directly with the transcriptional machinery. For example, in...
8.9K
Co-activators and Co-repressors
7.0K
Gene transcription is regulated by the synergistic action of several proteins that form a complex at a gene regulatory site. This is observed in eukaryotes, where the regulation of gene expression is a complex process. Regulatory proteins in eukaryotes can broadly be classified into two types – regulators that bind directly to specific DNA sequences and co-regulators that associate with regulatory proteins but cannot directly bind to the DNA. These co-regulators are further divided into...
7.0K
Eukaryotic Transcription Activators
10.5K
Transcription activators are proteins that promote the transcription of genes from DNA to RNA. In most cases, these proteins contain two separate domains ‒ a domain that binds to DNA and a domain for activating transcription; however, in some cases, a single domain is responsible for both binding and activation of transcription, as seen in the glucocorticoid receptor and MyoD.
The binding domains are capable of recognizing and interacting with regulatory sequences on the DNA. These...
The binding domains are capable of recognizing and interacting with regulatory sequences on the DNA. These...
10.5K
Master Transcription Regulators
6.1K
Master transcription regulators are regulatory proteins that are predominantly responsible for regulating the expression of multiple genes. Often these genes work in concert to drive a complex process. Activation of a master transcription regulator can lead to a cascade of transcriptional activation necessary for that outcome. These regulators can directly bind to the regulatory sequences of the various genes involved, or they can indirectly regulate transcription by binding to regulatory...
6.1K
Exon Recombination
3.1K
The evolution of new genes is critical for speciation. Exon recombination, also known as exon shuffling or domain shuffling, is an important means of new gene formation. It is observed across vertebrates, invertebrates, and in some plants such as potatoes and sunflowers. During exon recombination, exons from the same or different genes recombine and produce new exon-intron combinations, which might evolve into new genes.
Exon shuffling follows “splice frame rules.” Each exon...
Exon shuffling follows “splice frame rules.” Each exon...
3.1K
Canonical Wnt Signaling Pathway
8.6K
The gene encoding the main signaling molecules of the Wnt signaling pathways (the Wnt proteins) was discovered almost four decades ago by Nüsslein-Volhard and Wieschaus. They identified and originally named the gene "wingless" (wg) after a phenotype discovered during their landmark genetic screen in Drosophila for body pattern defects. At around the same time, another researcher named Harold Varmus found that a murine tumor virus activates the mammalian wg homolog, Int-1, which...
8.6K


