

Study with the several resources on Docsity
Earn points by helping other students or get them with a premium plan
Prepare for your exams
Study with the several resources on Docsity
Earn points to download
Earn points by helping other students or get them with a premium plan
Community
Ask the community for help and clear up your study doubts
Discover the best universities in your country according to Docsity users
Free resources
Download our free guides on studying techniques, anxiety management strategies, and thesis advice from Docsity tutors
The discovery of jumping genes by Barbara McClintock and their importance in genetic inheritance and evolution. It also describes the artificial synthesis of genes for yeast alanine t-RNA and bacterial tyrosine t-RNA by Khorana and his associates. the techniques used for gene synthesis and the number of base pairs in each gene. insights into the field of genetics and molecular biology.
Typology: Lecture notes
1 / 2
This page cannot be seen from the preview
Don't miss anything!
move from one location to another in a chromosome or even from one chromosome to another. These mobile elements or “Jumping genes” may occupy the position in the middle of other genes and disrupt them. McClintock had discovered the jumping genes before other geneticists began to realize their importance, indeed, the few workers understood her findings until the 1970s, after the mobile genes had discovered in E. coli. Strong evidences, now, suggest that all cells carry segments of DNA, called transposable elements or transposons or jumping genes, that are able to move from one site to another (Fig. 31.102 B). She found that a transposon can be inserted into the middle of a gene and make the gene no functional. These mobile genetic elements can function as natural mutagens that develop genetic differences. Thus, transposons would be powerful forces in evolution. In 1983, at the age of 81, she received the Nobel Prize for her significant work.
(a) Artificial synthesis of a gene for yeast alanine t-RNA: The yeast alanine t-RNA molecule is the first t-RNA molecule whose molecular structure was worked out by R.W. Holley and his coworkers in 1965. Khorana and his associates (1969) used this information for the deduction of the structure of the gene for yeast alanine t-RNA. They calculated that the gene for yeast alanine t-RNA has 77 base pairs. For the artificial synthesis of this gene they had before them the work of assembling the 77 pairs of nucleotides in exact order. Their technique involved first the chemical synthesis of short deoxynucleotide sequence, which then were joined by hydrogen bonds to form complementary strands. The second enzymatic synthesis was to join the double stranded pieces. For this purpose the DNA repair polynucleotide ligase was employed. enzyme, the (b) Artificial synthesis of a gene for bacterial tyrosine t-RNA: In 1975 Khorana and his associates have completed the synthesis of a gene for E. coli tyrosine t-RNA. Tyr. t-RNA has 126 pairs of nucleotides.