Related Experiment Video
Updated: May 9, 2026

10:44
Single Cell Multiplex Reverse Transcription Polymerase Chain Reaction After Patch-clamp
Published on: June 20, 2018
Sequences encoding identical peptides for the analysis and manipulation of coding DNA
1Facultad de Medicina, UAEM, Calle Ixtaccihuatl Esq Leñeros, Col. Los Volcanes C.P. 62350, Cuernavaca, Morelos, Mexico.
Bioinformation
|July 18, 2013
Summary
Sequences encoding identical peptides (SEIP) reveal species-specific DNA properties. SEIP manipulation shows potential for reconstructing coding DNA and heterologous protein expression.
Area of Science:
- Molecular Biology
- Bioinformatics
- Genomics
Background:
- Sequences encoding identical peptides (SEIP) offer a novel approach to study coding DNA properties independent of peptide sequence.
- Understanding these properties is crucial for both fundamental research and biotechnological applications like heterologous protein expression.
Purpose of the Study:
- To investigate coding DNA properties using SEIP across different species.
- To explore the potential of manipulating SEIP for creating new coding sequences and for heterologous protein expression.
Main Methods:
- Extraction and analysis of SEIP from human, E. coli, and D. melanogaster.
- Analysis of codon usage and intercodon dinucleotide tendencies.
- In silico manipulation of SEIP, including codon replacement experiments.
Main Results:
- Identified significant differences in codon usage and dinucleotide tendencies between human/E. coli and human/D. melanogaster SEIP.
- Demonstrated species-specific dicodon tendencies, limiting full codon replacement between species.
- Successfully reconstructed jellyfish green fluorescent protein (GFP) coding DNA using human SEIP fragments, proving the concept.
Conclusions:
- SEIP analysis effectively reveals intrinsic coding DNA properties and inter-species differences.
- SEIP manipulation provides a proof-of-principle for reconstructing coding DNA and holds promise for heterologous protein expression strategies.
Related Concept Videos
Sanger Sequencing
DNA sequencing is a fundamental technique that is routinely used in the biological sciences. This method can be applied to a range of questions at different scales - from the sequencing of a cloned DNA fragment or the study of a mutation in a gene up to whole-genome sequencing. However, despite the widespread use of sequencing today, it was not until 1977 that Fredrick Sanger and his collaborators developed the chain-termination method to decode DNA sequences. It relies on the separation of a...
From DNA to Protein
The flow of genetic information in cells from DNA to mRNA to protein is described by the central dogma, which states that genes specify the sequence of mRNAs, which in turn specify the sequence of amino acids making up all proteins. The decoding of one molecule to another is performed by specific proteins and RNAs. Because the information stored in DNA is so central to cellular function, it makes intuitive sense that the cell would make mRNA copies of this information for protein synthesis...
RNA-seq
RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases.
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while microarray-based...
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while microarray-based...
Complementary DNA
Overview
Next-generation Sequencing
The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features.
Maxam-Gilbert Sequencing
In the same year as the discovery of the Sanger sequencing method, another group of scientists, Allan Maxam and Walter Gilbert, demonstrated their chemical-cleavage method for DNA sequencing. The Maxam-Gilbert method relies on using different chemicals that can cleave the DNA sequence at specific sites, the separation of resulting DNA fragments of variable size using electrophoresis, and deciphering the DNA sequence from the resulting gel bands.
Challenges of the Maxam-Gilbert Method
The...
Challenges of the Maxam-Gilbert Method
The...

