<u>Answer:</u>
<em>B. Many genetic diseases would be curable.
</em>
<u>Explanation:</u>
Gene therapy is intended to acquaint hereditary material into cells in order to compensate for faulty or mutated genes or to make a helpful protein. On the off chance that a faulty gene makes a beneficial protein be flawed or missing, gene therapy might have the option to present a typical duplicate of the gene to reestablish the function of the protein.
A gene that is embedded straightforwardly into a cell as a rule doesn't work. Rather, a bearer or carrier called as a vector is hereditary built to insert the desired gene.
Answer:
is there a picture that we can use
The underlying molecular processes for 19 important DE miRNAs in the etiology of SCII were confirmed. The DE miRNAs could serve as potential intervention targets for SCII. Additionally, blocking microRNAs-3568 reduced apoptosis and preserved hind limb function after SCII, possibly via modulating GATA6, GATA4, and RBPJ in SCII.
microRNAs:
- Short non-coding RNAs called miRNAs (microRNAs) control post-transcriptional gene expression.
- SCII (spinal cord ischemia-reperfusion damage) is a medical condition that can lead to paralysis and paraplegia, among other serious effects. The development of SCII is influenced by aberrant microRNAs expression. Different microRNAs expression results could be caused by variations in the experimenters, filtering circumstances, control choice, and sequencing platform.
- The purpose of this study is to investigate the important differently expressed microRNAs (DE miRNAs) and the underlying molecular mechanism in SCII by methodically analyzing the available SCII microRNAs expression data. A thorough bioinformatics study of 23 representative rat SCII miRNA datasets from PubMed was carried out. On mi RDB, the target genes of important DE miRNAs were predicted.
- Functional enrichment and transcription factor binding analyses using the DAVID and T Fact S databases. Nine were increased (miR-144-3p, miR-3568, miR-204, miR-30c, miR-34c-3p, miR-155-3p, miR-200b, miR-463, and miR-760-5p) and ten were downregulated (this study found 19 important DE miRNAs involved in SCII) (miR-28-5p, miR-21-5p, miR-702-3p, miR-291a-3p, miR-199a-3p, miR-352, miR-743b-3p, miR-125b-2-3p, miR-129-1-3p, and miR-136).Target genes of the increased DE miRNAs underwent KEGG enrichment analysis, which identified the pathways primarily involved as being the cGMP-PKG and cAMP signaling pathways. According to KEGG enrichment analysis of the downregulated DE miRNAs' target genes, the main signaling pathways involved were the Chemokine and MAPK signaling pathways. The target genes of the increased DE miRNAs were clearly enriched in biological processes such brain development and the positive control of transcription from RNA polymerase II promoter, according to GO enrichment analysis.
- The majority of the target genes of the downregulated DE miRNAs were enriched in biological processes such intracellular signal transmission and the inhibition of cell growth. The transcription factor study revealed that the four transcription factors, SP1, GLI1, GLI2, and FOXO3, had significant regulatory effects on the main DE miRNAs' target genes. MiR-3568 stood out among the elevated DE miRNAs as being particularly intriguing. SCII results in significant neurological deficiencies in the lower extremities, but miR-3568 anti-miRNA oligonucleotides (AMOs) enhance neurological performance. When compared to the sham group, cleaved caspase-3 and Bax were significantly elevated in SCII, however the overexpression was inhibited by miR-3568 AMO. In contrast to cleaved caspase-3, Bcl-2 expression levels exhibited a pattern. Following the attenuation of this increase by SCII and microRNAs-3568 AMO, the expression of GATA6, GATA4, and RBPJ reduced.
Learn more about microRNAs here brainly.com/question/14979443
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Answer:
The correct answer would be His mitochondria lack the transport protein that moves pyruvate across the outer mitochondrial membrane.
In cellular respiration, glycolysis takes place in the cytoplasm of the cell and converts glucose into 2 molecules of pyruvate. Pyruvate is then transported into the mitochondria for further oxidation.
It is transported into the mitochondria with the help of transport protein pyruvate translocase where it is decorboxylated to produce acetyl-CoA. This acetyl-CoA then enters the Krebs cycle to produce ATP (adenosine triphosphate) with the help of oxidative phosphorylation, electron transport chain and chemiosmosis.
In absence of this transport protein, the cell can not completely oxidize the glucose or carbohydrate. It switches to the metabolism of fats and amino acids in order to meet the energy demands of the cell.
