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TRANSLATION
TRANSLATION

... The small subunit of the ribosome recognizes the 5' cap on the mRNA transcript and binds to the RNA. The ribosome will position itself at AUG (the first codon read for every protein) ...
5.4 Translation
5.4 Translation

... The small subunit of the ribosome recognizes the 5' cap on the mRNA transcript and binds to the RNA. The ribosome will position itself at AUG (the first codon read for every protein) ...
Epigenetics - UNM Biology
Epigenetics - UNM Biology

EOC REVIEW QUESTIONS
EOC REVIEW QUESTIONS

... How is the genetic blueprint that makes you who you are transferred faithfully from one cell to the next? Why are the offspring of two parents different than one another? What happens when something goes wrong during meiosis? How do genetic traits get passed from parent to offspring? If two parents ...
Plant Nuclear Genome Size Variation
Plant Nuclear Genome Size Variation

... Not a substantial contributor to variation in genome size ...
2013 Training Handout
2013 Training Handout

... There are 64 possible three base codons – 61 are codes for one of the 20 amino acids The three remaining codons are termed stop codons because the signal the end of a peptide segment Notice that many of the amino acids have more than one codon A three base code on the DNA produces the mRNA codon The ...
Ch._3_Powerpoint.pptx
Ch._3_Powerpoint.pptx

... In meiosis one cell divides into 4 new cells Each cell has half the number of chromosomes as the parent cell ...
Document
Document

... the nucleus so the code is transcribed from DNA into mRNA, mRNA then leaves the cell nucleus to go to the ribosome in the cytoplasm) ...
Document
Document

... Retroviruses can only infect replicative cells Transfection cannot be done in non-replicative cells Best system to study gene expression in primary non-replicative cells Allows for a direct comparison of results obtained with transformed cell lines and primary cells ...
August 2007
August 2007

... Color blindness is linked to testosterone levels. Color blindness is the dominant condition in males. Human females have two X chromosomes. The gene for color blindness is autosomal. ...
Slide 1
Slide 1

... Avery and Hersey-chase Experiments ...
Lecture 10 in molecular biology by Dr. Sawsan Saijd
Lecture 10 in molecular biology by Dr. Sawsan Saijd

... DNA methylation: is a biochemical process involving the addition of a methyl group (CH3) to the cytosine or adenine DNA nucleotides. The main function of DNA methylation in bacteria is to provide a mechanism, which protects the cell from the effect of foreign DNA introduction. Restriction endonuclea ...
FREE Sample Here
FREE Sample Here

... E. Inheritance of the white-eyed trait was the same for female and male flies. Ans: D 16. Calvin Bridges, an associate of Morgan’s, found further evidence that genes were located on chromosomes. Which of the following is not a component of his study? 1. He crossed white-eyed females (XwXw) with red- ...
Exam - National Biology Competition
Exam - National Biology Competition

... 20. In Mendel’s experiments with pea plants, he described two unlinked genes that controlled seed shape and seed colour. He crossed plants that were homozygous for green and wrinkled seeds with plants that were homozygous for yellow and round seeds. All of the resulting F1 plants had yellow and roun ...
Q3 - Franklin County Community School Corporation
Q3 - Franklin County Community School Corporation

... Explain how and why the genetic code is universal Describe the structure and function of DNA Differentiate between replication, transcription, and translation. Draw and label the parts of DNA Replication Draw and explain transcription and translation Describe how genetic recombination increases gene ...
FREE Sample Here
FREE Sample Here

... E. Inheritance of the white-eyed trait was the same for female and male flies. Ans: D 16. Calvin Bridges, an associate of Morgan’s, found further evidence that genes were located on chromosomes. Which of the following is not a component of his study? 1. He crossed white-eyed females (XwXw) with red- ...
Misconceptions, misunderstandings and questions students
Misconceptions, misunderstandings and questions students

... are included below. A powerpoint presentation used for discussion during the lab is provided as an accompanying document (Strawberries.ppt). Short Cycle and Genetics Unit Assessments gave additional evaluation for this investigation. ...
What is Genetic Engineering?
What is Genetic Engineering?

...  _______ gene from one creature into other creature’s DNA  _______ new chromosome into organism  organism _______ new gene as if it were its own  organism _______ gene as if it were its own  _____________________________________: Remember: we all use the same genetic code! ...
Document
Document

... (remember-DNA never leaves the nucleus so the code is transcribed from DNA into mRNA, mRNA then leaves the cell nucleus to go to the ribosome in the cytoplasm) ...
Cells and DNA Table of Contents
Cells and DNA Table of Contents

... For more information about chromosomes: Genetics Home Reference provides information about each human chromosome (http://ghr.nlm.nih.gov/chromosomes) written in lay language. The Centre for Genetics Education offers a fact sheet that introduces genes and chromosomes (http://www.genetics.edu.au/Info ...
Chapter 15: Translation of mRNA
Chapter 15: Translation of mRNA

... After introducing the genetic code, tRNAs and the ribosome, we are prepared to discuss the process of translation. Note that translation involves three stages – initiation, elongation, and termination. Although this is the same terminology as was used in transcription, the processes are very differe ...
Chapter 13 DNA - Pearson Places
Chapter 13 DNA - Pearson Places

... Just one missing nucleotide in the DNA sequence that codes for haemoglobin production causes a defective molecule in red blood cells, so that they change shape where oxygen concentration is low. The red blood cells have a shorter lifespan and this causes anaemia. ...
ppt
ppt

... 2. Cut it with restriction enzymes – create a DNA ‘library’ of the fragments 3. Insert it into a vector, creating a recombinant DNA molecule 4. Insert the vector into a host cell 5. Create a population of cells (clone) that have this new DNA. 6. The DNA or protein product can be isolated and purifie ...
C2005/F2401 `07 -- Lecture 15 -- Last Edited
C2005/F2401 `07 -- Lecture 15 -- Last Edited

... what is true of E. coli true of the elephant? (Monod liked to think so.) a. Transcriptional control is common. It is the primary way, but not the only way, to regulate protein synthesis. b. Two part switches, consisting of a protein and DNA site are very, very common. The situation is often more com ...
pdf
pdf

... Silencers are cis-acting regulatory sequences that reduce the expression from a promoter in a manner independent of position or orientation - i.e. they have the opposite effect of an enhancer. Two examples are the silencers that prevent expression of the a or α genes at the silent loci of the mating ...
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Primary transcript



A primary transcript is the single-stranded ribonucleic acid (RNA) product synthesized by transcription of DNA, and processed to yield various mature RNA products such as mRNAs, tRNAs, and rRNAs. The primary transcripts designated to be mRNAs are modified in preparation for translation. For example, a precursor messenger RNA (pre-mRNA) is a type of primary transcript that becomes a messenger RNA (mRNA) after processing.There are several steps contributing to the production of primary transcripts. All these steps involve a series of interactions to initiate and complete the transcription of DNA in the nucleus of eukaryotes. Certain factors play key roles in the activation and inhibition of transcription, where they regulate primary transcript production. Transcription produces primary transcripts that are further modified by several processes. These processes include the 5' cap, 3'-polyadenylation, and alternative splicing. In particular, alternative splicing directly contributes to the diversity of mRNA found in cells. The modifications of primary transcripts have been further studied in research seeking greater knowledge of the role and significance of these transcripts. Experimental studies based on molecular changes to primary transcripts the processes before and after transcription have led to greater understanding of diseases involving primary transcripts.
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