c. An area where the nucleus is synthesized

The ribosomes are placed at two places. They are suspended in cytosol and are also bound to endoplasmic reticulum. These two ribosomes are called free ribosomes and bound ribosomes respectively. In both places, ribosomes form polysomes as aggregates. Free ribosomes prepare that function in cytosol and the bound ribosomes create which are exported or even included in the membrane of You do not have access to view this node. One of the interesting facts is that both free ribosomes and bound ribosomes are interchangeable and depending upon the metabolic requirements, the number of cells varies. The structure of both free ribosomes and bound ribosomes is similar.

The main stages of protein synthesis are transcription and translation.

The cell unit consists of cell membrane or plasma membrane in which various organelles are present in suspension. At the center is located the nucleus. Although mitochondria is considered the power house of cell, other parts like the ribosomes or golgi apparatus too have their own functions which help in the complete cell functioning. Ribosomes help in the synthesis of the cell and the sites at which genetic code is synthesized to molecules.


30. Ribosomes are the site of synthesis of:

This sequence is located 8 b (b = bases or nucleotides) upstream (i.e.

[An ester bond is an oxygen atom bridge between two carbon atoms in which one of
the carbon atoms is a C=O or carbonyl group: -C-O-C=O.] Each tRNA carries a specific sequence of three nucleotides, called
an anticodon.


What is the role of messenger RNA and ribosomes in protein synthesis

RNAi constructs can be designed to target any knowngene. As they make use of a conserved biological silencing pathway,they are a particularly effective method to inhibit aberrant geneexpression that results in pathogenesis. The sequence specificityof the RNAi mechanism provides a high specificity required fortargeted therapies, overcoming the side effects of severaltraditional therapies. Specific gene silencing can be achieved inmany sorts of cell systems using chemically synthesized smallinterference RNA (siRNA) or DNA vector-based shRNA. Functionalgenomics using RNAi has facilitated the rate in which genes areassigned function and thereby expedited the identification ofpotential therapeutic targets for some gene related diseases(–). Importantly, several RNAi-basedtherapies are on the way to being developed (). Doxycycline-controlled tet-onlentiviral system enables the reversible and body-wide expressionof shRNAs (,) and offers the opportunity to reversethe induced gene knockdown at a given time. This property of theshRNA system offers unique applications to study gene function inanimal experiments that cannot be achieved with knockouttechnologies (,). Although lentivirus vectors has beenused for several years, the use of Tet-on lentiviral vectorexpressing shRNA as a therapeutic tool for rhabdomyosarcoma has notbeen clearly explored.

Are ribosomes the sites of protein synthesis

Ribosomes are one of the organelles made up of RNA, a type of . Ribosomes perform the function of assembling the cell . The production efficacy of a cell decides the number of ribosomes which can be sometimes in millions. Ribosomes are commonly called as the sites of synthesis. Ribosomes are found attached to the in the cell(bound ribosomes) or exist freely in which case they are called free ribosomes. Both the free and bound ribosomes can be interchanged and based on the bodies requirement are converted accordingly.

Are ribosomes site of protein synthesis

The mRNA sequence of human Mirk (GenBank acc. no.:NM_004714) was placed in Ambion online RNAi Designer to designsiRNA. Since not every working siRNA sequence is equally effectivewhen incorporated into shRNA (), we selected three optimal siRNAs indifferent target sequences. One scrambled shRNA control wasspecifically designed. All four sequences were aligned using theGenBank BLAST program, no other homologous sequences matched exceptthe Mirk gene. To obtain the double-stranded RNA configurationrequired for short hairpin RNA formation from single-stranded RNA,we linked a 19-bp sense siRNA sequence to its complementaryantisense sequence via a 9-bp loop region and combine it withadditional two T nucleotides, which is flanked by restrictionenzyme recognition sequences and their protective bases (). Two complementary single-strandedDNA oligonucleotides of the four shRNAs were chemically synthesizedby Shanghai Genechem Co. Ltd. These oligonucleotides were annealedto produce double-stranded oligonucleotides ().