Christopher Chetsanga

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Christopher J Chetsanga
Christopher Chetsanga.jpg
Christopher Chetsanga demonstrates to students how to do an experiment
Born (1935-08-22) 22 August 1935 (age 88)
Nationality Zimbabwean
Alma mater University of California
Pepperdine University
University of Toronto
Known forDiscovery of two enzymes involved in DNA repair
Academic administration
Scientific career
Fields Biochemistry
Molecular Biology
Institutions Harvard University
University of Michigan
University of Zimbabwe
Scientific and Industrial Research and Development Centre
Zimbabwe Ezekiel Guti University

Christopher J. Chetsanga (born 1935 in Murehwa, Rhodesia) is a prominent Zimbabwean scientist who is a member of the African Academy of Sciences and The World Academy of Sciences. [1] [2] He discovered two enzymes involved in DNA repair. [3] [4] He has also held various academic administrative posts like Vice-Chancellor, Director and Dean.

Contents

Biography

Chetsanga was born in Murewa, Zimbabwe on 22 August 1935, [5] and was baptised in 1948. In his youth, he was educated at Nhowe Mission, and went on to study at University of California, Berkeley where he received his BSc in 1965. Chetsanga also studied for a period at Pepperdine University. [6] In 1969, he received his MSc and PhD in biochemistry and molecular biology from University of Toronto [6] before becoming a post doctoral fellow at Harvard University between 1969 and 1972. [5] Between 1972 and 1983 he became a professor at the University of Michigan, then in 1983 he left to become the senior lecturer in Biochemistry for University of Zimbabwe. [7] In 1990, President Robert Mugabe awarded him President’s Award for Distinguished Contribution to Science and Technology. [5] [8] [9] Has also awarded the Order of the Star of Zimbabwe. [10] He is presently the vice chancellor at Zimbabwe Ezekiel Guti University. [11]

In 2004, when the Zimbabwe Academy of Sciences was formed, Chetsanga was appointed the first president of the academy. [12] Chetsanga advocated the use of genetically modified food sources as a possible solution for food shortages in Africa in 2020. [13]

Scientific Achievements

Chetsanga has discovered two enzymes involved in the repair of damaged DNA: firstly, formamidopyrimidine DNA glycosylase, which removes damaged 7-methylguanine from DNA (1979), [4] and secondly, purine imidazole-ring cyclase, which re-closes imidazole rings of guanine and adenine damaged by x-irradiation (1985). [3]

According to Chetsanga, his research focus in his scientific career has been on DNA and RNA structural and functional details as they relate to cellular metabolism and disease development. [14]

Select publications

Related Research Articles

<span class="mw-page-title-main">Cytosine</span> Chemical compound in nucleic acids

Cytosine is one of the four nucleobases found in DNA and RNA, along with adenine, guanine, and thymine. It is a pyrimidine derivative, with a heterocyclic aromatic ring and two substituents attached. The nucleoside of cytosine is cytidine. In Watson-Crick base pairing, it forms three hydrogen bonds with guanine.

<span class="mw-page-title-main">Nucleotide</span> Biological molecules that form the building blocks of nucleic acids

Nucleotides are organic molecules composed of a nitrogenous base, a pentose sugar and a phosphate. They serve as monomeric units of the nucleic acid polymers – deoxyribonucleic acid (DNA) and ribonucleic acid (RNA), both of which are essential biomolecules within all life-forms on Earth. Nucleotides are obtained in the diet and are also synthesized from common nutrients by the liver.

<span class="mw-page-title-main">Purine</span> Heterocyclic aromatic organic compound

Purine is a heterocyclic aromatic organic compound that consists of two rings fused together. It is water-soluble. Purine also gives its name to the wider class of molecules, purines, which include substituted purines and their tautomers. They are the most widely occurring nitrogen-containing heterocycles in nature.

Pyrimidine is an aromatic, heterocyclic, organic compound similar to pyridine. One of the three diazines, it has nitrogen atoms at positions 1 and 3 in the ring. The other diazines are pyrazine and pyridazine.

<span class="mw-page-title-main">Uracil</span> Chemical compound of RNA

Uracil is one of the four nucleobases in the nucleic acid RNA. The others are adenine (A), cytosine (C), and guanine (G). In RNA, uracil binds to adenine via two hydrogen bonds. In DNA, the uracil nucleobase is replaced by thymine (T). Uracil is a demethylated form of thymine.

<span class="mw-page-title-main">Nucleobase</span> Nitrogen-containing biological compounds that form nucleosides

Nucleobases are nitrogen-containing biological compounds that form nucleosides, which, in turn, are components of nucleotides, with all of these monomers constituting the basic building blocks of nucleic acids. The ability of nucleobases to form base pairs and to stack one upon another leads directly to long-chain helical structures such as ribonucleic acid (RNA) and deoxyribonucleic acid (DNA). Five nucleobases—adenine (A), cytosine (C), guanine (G), thymine (T), and uracil (U)—are called primary or canonical. They function as the fundamental units of the genetic code, with the bases A, G, C, and T being found in DNA while A, G, C, and U are found in RNA. Thymine and uracil are distinguished by merely the presence or absence of a methyl group on the fifth carbon (C5) of these heterocyclic six-membered rings. In addition, some viruses have aminoadenine (Z) instead of adenine. It differs in having an extra amine group, creating a more stable bond to thymine.

<span class="mw-page-title-main">Hypoxanthine</span> Chemical compound

Hypoxanthine is a naturally occurring purine derivative. It is occasionally found as a constituent of nucleic acids, where it is present in the anticodon of tRNA in the form of its nucleoside inosine. It has a tautomer known as 6-hydroxypurine. Hypoxanthine is a necessary additive in certain cells, bacteria, and parasite cultures as a substrate and nitrogen source. For example, it is commonly a required reagent in malaria parasite cultures, since Plasmodium falciparum requires a source of hypoxanthine for nucleic acid synthesis and energy metabolism.

<span class="mw-page-title-main">Ribonucleotide</span> Nucleotide containing ribose as its pentose component

In biochemistry, a ribonucleotide is a nucleotide containing ribose as its pentose component. It is considered a molecular precursor of nucleic acids. Nucleotides are the basic building blocks of DNA and RNA. Ribonucleotides themselves are basic monomeric building blocks for RNA. Deoxyribonucleotides, formed by reducing ribonucleotides with the enzyme ribonucleotide reductase (RNR), are essential building blocks for DNA. There are several differences between DNA deoxyribonucleotides and RNA ribonucleotides. Successive nucleotides are linked together via phosphodiester bonds.

In molecular biology, biosynthesis is a multi-step, enzyme-catalyzed process where substrates are converted into more complex products in living organisms. In biosynthesis, simple compounds are modified, converted into other compounds, or joined to form macromolecules. This process often consists of metabolic pathways. Some of these biosynthetic pathways are located within a single cellular organelle, while others involve enzymes that are located within multiple cellular organelles. Examples of these biosynthetic pathways include the production of lipid membrane components and nucleotides. Biosynthesis is usually synonymous with anabolism.

<span class="mw-page-title-main">AP site</span> Biochemical site of damaged DNA or RNA

In biochemistry and molecular genetics, an AP site, also known as an abasic site, is a location in DNA that has neither a purine nor a pyrimidine base, either spontaneously or due to DNA damage. It has been estimated that under physiological conditions 10,000 apurinic sites and 500 apyrimidinic may be generated in a cell daily.

<span class="mw-page-title-main">Purine nucleoside phosphorylase</span> Enzyme

Purine nucleoside phosphorylase, PNP, PNPase or inosine phosphorylase is an enzyme that in humans is encoded by the NP gene. It catalyzes the chemical reaction

<span class="mw-page-title-main">Phosphoribosyl pyrophosphate</span> Chemical compound

Phosphoribosyl pyrophosphate (PRPP) is a pentose phosphate. It is a biochemical intermediate in the formation of purine nucleotides via inosine-5-monophosphate, as well as in pyrimidine nucleotide formation. Hence it is a building block for DNA and RNA. The vitamins thiamine and cobalamin, and the amino acid tryptophan also contain fragments derived from PRPP. It is formed from ribose 5-phosphate (R5P) by the enzyme ribose-phosphate diphosphokinase:

Purine metabolism refers to the metabolic pathways to synthesize and break down purines that are present in many organisms.

The enzyme purine imidazole-ring cyclase (EC 4.3.2.4) catalyzes the chemical reaction

<span class="mw-page-title-main">Uracil-DNA glycosylase</span> Enzyme that repairs DNA damage

Uracil-DNA glycosylase is an enzyme. Its most important function is to prevent mutagenesis by eliminating uracil from DNA molecules by cleaving the N-glycosidic bond and initiating the base-excision repair (BER) pathway.

<span class="mw-page-title-main">DNA-3-methyladenine glycosylase</span> Protein-coding gene in the species Homo sapiens

DNA-3-methyladenine glycosylase also known as 3-alkyladenine DNA glycosylase (AAG) or N-methylpurine DNA glycosylase (MPG) is an enzyme that in humans is encoded by the MPG gene.

<span class="mw-page-title-main">DNA polymerase eta</span> Protein-coding gene in the species Homo sapiens

DNA polymerase eta, is a protein that in humans is encoded by the POLH gene.

<span class="mw-page-title-main">5-Aminoimidazole ribotide</span> Chemical compound

5′-Phosphoribosyl-5-aminoimidazole is a biochemical intermediate in the formation of purine nucleotides via inosine-5-monophosphate, and hence is a building block for DNA and RNA. The vitamins thiamine and cobalamin also contain fragments derived from AIR. It is an intermediate in the adenine pathway and is synthesized from 5′-phosphoribosylformylglycinamidine by AIR synthetase.

<span class="mw-page-title-main">Stephen J. Benkovic</span> American chemist

Stephen James Benkovic is an American chemist known for his contributions to the field of enzymology. He holds the Evan Pugh University Professorship and Eberly Chair in Chemistry at The Pennsylvania State University. He has developed boron compounds that are active pharmacophores against a variety of diseases. Benkovic has concentrated on the assembly and kinetic attributes of the enzymatic machinery that performs DNA replication, DNA repair, and purine biosynthesis.

DNA-formamidopyrimidine glycosylase is an enzyme with systematic name DNA glycohydrolase . FPG is a base excision repair enzyme which recognizes and removes a wide range of oxidized purines from correspondingly damaged DNA. It was discovered by Zimbabwean scientist Christopher J. Chetsanga in 1975.

References

  1. AAS. "Chetsanga, J. Christophe, Prof." Archived 2014-09-03 at the Wayback Machine , Fellow of AAS since 1986; Biochemistry and Molecular Biology, Nairobi, unknown. Retrieved on 28 August 2014.
  2. "Christopher Chetsanga - Pepperdine's Outstanding Alumni Abroad | Pepperdine University". www.pepperdine.edu. Retrieved 2022-10-03.
  3. 1 2 Chetsanga, C.J.; Grigorian, C. (1985). "In situ enzymatic reclosure of opened imidazole rings of purines in DNA damaged by gamma-irradiation". Proceedings of the National Academy of Sciences of the United States of America. 82 (3): 633–637. Bibcode:1985PNAS...82..633C. doi: 10.1073/pnas.82.3.633 . JSTOR   25324. PMC   397099 . PMID   3856219.
  4. 1 2 Chetsanga, C.J.; Lindahl, T. (1979). "Release of 7-methylguanine residues whose imidazole rings have been opened from damaged DNA by a DNA glycosylase from Escherichia coli". Nucleic Acids Res. 6 (11): 3673–84. doi:10.1093/nar/6.11.3673. PMC   327965 . PMID   386277.
  5. 1 2 3 "CHETSANGA Christopher J." TWAS. The World Academy of Science. Retrieved 19 July 2020.
  6. 1 2 David Mubvumbi, Paradzayi (2016). Christianity And Traditional Religions Of Zimbabwe : Contrasts And Similarities. Westbow Press. ISBN   9781512745108 . Retrieved 19 July 2020.
  7. "Prof. Christopher James Chetsanga". University of Zimbabwe. Retrieved 19 July 2020.
  8. "EAI International Conference for Research, Innovation and Development for Africa". EAI. June 2017. Retrieved 19 July 2020.
  9. "Chetsanga Christopher". African Academy of Sciences. Retrieved 19 July 2020.
  10. Ziana, New (2021-08-09). "Zimbabwe awards civilian heroes - New Ziana" . Retrieved 2022-10-03.
  11. "Zimbabwe Ezekiel Guti University - Home". www.zegu.ac.zw. Retrieved 2021-06-02.
  12. "OWSD Zimbabwe National Chapter is Launched". Organization for women in science for the developing world. 20 November 2018. Retrieved 19 July 2020.
  13. "GMB to import GMO Maize". NewsdzeZimbabwe. 23 April 2020. Retrieved 19 July 2020.
  14. "Christopher J. Chetsanga". Pepperdine. Retrieved 19 July 2020.