عنوان

Transcript, Structural, and Histologic Characterization of a Novel EF-Hand Protein and Its Isoform Specific to the Ambulacraria Clade

Number

TLpq2407361698

.Language of Text, Soundtrack etc

انگلیسی

Title Proper

Transcript, Structural, and Histologic Characterization of a Novel EF-Hand Protein and Its Isoform Specific to the Ambulacraria Clade

General Material Designation

[Thesis]

First Statement of Responsibility

Soto Acabá, Arisnel

Subsequent Statement of Responsibility

García-Arrarás, José E.

Name of Publisher, Distributor, etc.

University of Puerto Rico, Rio Piedras (Puerto Rico)

Date of Publication, Distribution, etc.

2020

Specific Material Designation and Extent of Item

205

Dissertation or thesis details and type of degree

Ph.D.

Body granting the degree

University of Puerto Rico, Rio Piedras (Puerto Rico)

Text preceding or following the note

2020

Text of Note

Transcriptomic databases have become one of the main sources for protein discovery. In our studies of transcripts from normal echinoderms, we have identified several transcripts that have attracted our attention. One of these is a previously unidentified transcript (Orpin) that appeared to be upregulated during intestinal regeneration. In Chapter 2, using bioinformatics tools we: (1) identified a second Orpin sequence (2) describe their motifs and domains, and perform phylogenetic analyses that suggest that Orpins might comprise a novel subfamily of EF-hand containing proteins specific to the Ambulacraria clade. Semi-quantitative RT-PCR analyses revealed that Orpin mRNAs are expressed in various tissues but no significant differential expression was found in regenerating tissues. In Chapter 3 we expressed and purified genetically modified versions of Orpin to further characterize this EF-hand protein. We developed two protocols: The first protocol consisted in the production of His-OBSm, which is His tagged with two additional genetic modifications: the deletion of the signal peptide encoding sequence and the addition of a 25 residues peptide from the pET200 plasmid vector. These modifications made possible the purification of a soluble recombinant version of Orpin B. The second protocol was developed to produce a soluble recombinant Orpin that best resembled the original protein. This protocol consisted of the expression of a GST-Orpin lacking the signal peptide region. For this protocol, we tested different parameters that affect protein expression, including, additives, host cells, growth media and supplementation, and protein extraction methods. The best parameters were identified and used to obtain a soluble Orpin form. We propose that the developed strategies can be used to increase the soluble expression and purification of other EF-hand proteins that are difficult to express by standard methods. In chapter 4 we produced antibodies against His-OBSm and used these to identify the cells expressing the protein in H. glaberrima tissues. Antibody specificity was tested through Western Blots. Finally, we investigated the effect of the Wnt signaling pathway on Orpin mRNA expression in regenerating gut explants and found an apparent decrease expression of an Orpin B isoform following Wnt/B-catenin pathway activation.

Developmental biology

Molecular biology

Zoology

García-Arrarás, José E.

Soto Acabá, Arisnel

Electronic name

p

[Thesis]

276903

a

Y