Lethal allele
Lethal alleles (also referred to as lethal or lethals) are alleles that cause the death of the organism that carries them. They are usually a result of mutations in genes that are essential for growth or development.[1] Lethal alleles may be recessive, dominant, or conditional depending on the gene or genes involved.
Lethal alleles can be embryonically lethal, in which the fetus will never survive to term, or may be lethal perinatally or postnatally after an extended period of apparently normal development. Embryonically lethal alleles are a cause of non-Mendelian patterns of inheritance, such as the observation of traits in a 2:1 ratio.
History
[edit]
Lethal alleles were first discovered by Lucien Cuénot in 1905 while studying the inheritance of coat colour in mice. The agouti gene in mice is largely responsible for determining coat colour. The wild-type allele produces a blend of yellow and black pigmentation in each hair of the mouse. This yellow and black blend may be referred to as 'agouti' in colour.[3] One of the mutant alleles of the agouti gene results in mice with a much lighter, yellowish colour. When these yellow mice were crossed with homozygous wild-type mice, a 1:1 ratio of yellow and dark grey offspring were obtained. This indicated that the yellow mutation is dominant, and all the parental yellow mice were heterozygotes for the mutant allele.
By mating two yellow mice, Cuénot expected to observe a usual 1:2:1 Mendelian ratio of homozygous agouti to heterozygous yellow to homozygous yellow. Instead, he always observed a 1:2 ratio of agouti to yellow mice. He was unable to produce any mice that were homozygous for the yellow agouti allele.
It was not until 1910 that W. E. Castle and C. C. Little confirmed Cuénot's work, further demonstrating that one quarter of the offspring were dying during embryonic development. This was the first documented example of a recessive lethal allele.
Types of lethal allele
[edit]Recessive lethals
[edit]A pair of identical alleles that are both present in an organism that ultimately results in death of that organism are referred to as recessive lethal alleles. Though recessive lethals may code for dominant or recessive traits, they are only fatal in the homozygous condition.
Heterozygotes will sometimes display a form of diseased phenotype, as in the case of achondroplasia.[4] One mutant lethal allele can be tolerated, but having two results in death. In the case of homozygous achondroplasia, death almost invariably occurs before birth or in the perinatal period. Not all heterozygotes for recessive lethal alleles will show a mutant phenotype, as is the case for cystic fibrosis carriers. If two cystic fibrosis carriers have children, they have a 25 percent chance of producing offspring having two copies of the lethal allele, eventually resulting in the death of the child.[5] Another example are the BRCA mutations; inheriting one defective BRCA allele results in a greatly increased risk of breast cancer and ovarian cancer, while inheriting both defective alleles will result in a severe form of Fanconi anemia (FA-S for BRCA1, FA-D1 for BRCA2) that is embryonically lethal in most cases. Survivors of homozygous or biallelic BRCA mutations almost never survive to adulthood. [6] For live cases, inheriting both mutations lead to a grave prognosis where survival almost never extends beyond childhood.[7]
Another example of a recessive lethal allele occurs in the Manx cat. Manx cats possess a heterozygous mutation resulting in a shortened or missing tail. Crosses of two heterozygous Manx cats result in two-thirds of surviving offspring displaying the heterozygous shortened tail phenotype, and one-third of surviving offspring of normal tail length that is homozygous for a normal allele. Homozygous offspring for the mutant allele cannot survive birth and are therefore not seen in these crosses.[8]
Dominant lethals
[edit]Alleles that need only be present in one copy in an organism to be fatal are referred to as dominant lethal alleles. These alleles are not commonly found in populations because they usually result in the death of an organism before it can transmit its lethal allele on to its offspring.[4] An example in humans of a dominant lethal allele is Huntington's disease, a rare neurodegenerative disorder that ultimately results in death. However, because of its late-onset (i.e., often after reproduction has already occurred), it is able to be maintained in populations. A person exhibits Huntington's disease when they carry a single copy of a repeat-expanded Huntington allele on chromosome 4.[9]
Conditional lethals
[edit]Alleles that will only be fatal in response to some environmental factor are referred to as conditional lethals. One example of a conditional lethal is favism, a sex-linked inherited condition that causes the carrier to develop hemolytic anemia when they eat fava beans.[4]
An infection of an E. coli host cell by a bacteriophage (phage) T4 temperature sensitive (ts) conditionally lethal mutant at a high restrictive temperature leads to lack of viable phage production. However growth of such mutants can still occur at a lower temperature. Such conditionally lethal ts mutants have been used to identify and characterize the function of many of the phage's genes.[10] Thus genes employed in the repair of DNA damages were identified using ts mutants,[11][12] as well as genes affecting genetic recombination.[13][14] For example, growing a ts DNA repair mutant at an intermediate temperature will allow some progeny phage to be produced. However, if that ts mutant is irradiated with UV light, its survival will be more strongly reduced compared to the reduction of survival of irradiated wild-type phage T4. In addition, cold sensitive conditional lethal mutants able to grow at high temperatures, but unable to grow at low temperatures, were also isolated in phage T4.[15] These cold sensitive conditional lethal mutants also defined a set of phage genes. Another class of conditional lethal phage T4 mutants, called amber mutants, are able to grow on some strains of E. coli but not on others.[10][16][17] These mutants were also used to initially identify and characterize many of the phage T4 genes, including genes whose encoded proteins function in DNA repair, genetic recombination, DNA replication and molecular morphogenesis. In addition, it was found that an amber mutation produces a "nonsense codon" within a gene that causes polypeptide chain termination during translation. This finding provided insight into a significant aspect of the genetic code.
See also
[edit]References
[edit]- ^ Gluecksohn-Waelsch, Salome (1963). "Lethal Genes and Analysis of Differentiation". Science. 142 (3597): 1269–76. Bibcode:1963Sci...142.1269G. doi:10.1126/science.142.3597.1269. PMID 14074837. S2CID 46113268.
- ^ Mouse Genomes Informatic
- ^ Hartwell, Leland; Hood, Leroy; Goldberg, Michael; Reynolds, Ann; Silver, Lee; Karagiannis, Jim; Papaconstantinou, Maria (2014). Genetics: From Genes to Genomes. Canada: McGraw-Hill Ryerson. pp. 39–42. ISBN 978-0-07-094669-9.
- ^ a b c Lobo, I (2008). "Mendelian Ratios and Lethal Genes". Nature Education. 1 (1): 138.
- ^ Ratjen, Felix; Döring, Gerd (February 2003). "Cystic fibrosis". Lancet. 361 (9358): 681–689. doi:10.1016/S0140-6736(03)12567-6. PMID 12606185. S2CID 24879334.
- ^ Sawyer SL, Tian L, Kahkonen M, Schwartzentruber J, Kircher M, Majewski J, Dyment DA, Innes AM, Boycott KM, Moreau LA, Moilanen JS, Greenberg RA (2014). "Biallelic Mutations in BRCA1 Cause a New Fanconi Anemia Subtype". Cancer Discov. 5 (2): 135–42. doi:10.1158/2159-8290.CD-14-1156. PMC 4320660. PMID 25472942.
- ^ Maxwell, KN, Patel, V, Nead, KT, et al. (2013). "Fanconi anemia caused by biallelic inactivation of BRCA2 can present with an atypical cancer phenotype in adulthood". Clinical Genetics. 103 (1): 119–124. doi:10.1111/cge.14231. PMC 9742260. PMID 36089892. S2CID 252198281.
- ^ Robinson, R (1993). "Expressivity of the Manx Gene in Cats". J Hered. 84 (3): 170–2. doi:10.1093/oxfordjournals.jhered.a111311. PMID 8228170.
- ^ Roos, Raymund AC (2010). "Huntington's disease: a clinical review". Orphanet Journal of Rare Diseases. 5 (1): 40. doi:10.1186/1750-1172-5-40. PMC 3022767. PMID 21171977.
- ^ a b Edgar RS, Epstein RH (February 1965). "The genetics of a bacterial virus". Sci Am. 212: 70–8. doi:10.1038/scientificamerican0265-70. PMID 14272117.
- ^ Baldy MW (February 1970). "The UV sensitivity of some early-function temperature-sensitive mutants of phage T4". Virology. 40 (2): 272–87. doi:10.1016/0042-6822(70)90403-4. PMID 4909413.
- ^ Baldy MW, Strom B, Bernstein H (March 1971). "Repair of alkylated bacteriophage T4 deoxyribonucleic acid by a mechanism involving polynucleotide ligase". J Virol. 7 (3): 407–8. doi:10.1128/JVI.7.3.407-408.1971. PMC 356131. PMID 4927528.
- ^ Bernstein H (August 1967). "The effect on recombination of mutational defects in the DNA-polymerase and deoxycytidylate hydroxymethylase of phage T4D". Genetics. 56 (4): 755–69. doi:10.1093/genetics/56.4.755. PMC 1211652. PMID 6061665.
- ^ Bernstein H (1968). "Repair and recombination in phage T4. I. Genes affecting recombination". Cold Spring Harb Symp Quant Biol. 33: 325–31. doi:10.1101/sqb.1968.033.01.037. PMID 4891972.
- ^ Scotti PD (1968). "A new class of temperature conditional lethal mutants of bacteriophage T4D". Mutat Res. 6 (1): 1–14. doi:10.1016/0027-5107(68)90098-5. PMID 4885498.
- ^ Epstein RH, Bolle A, Steinberg CM, Stahl FW (March 2012). "Amber mutants of bacteriophage T4D: their isolation and genetic characterization". Genetics. 190 (3): 831–40. doi:10.1534/genetics.112.138438. PMC 3296251. PMID 22518878.
- ^ Epstein RH, Bolle A, Steinberg CM (March 2012). "Amber mutants of bacteriophage T4D: their isolation and genetic characterization". Genetics. 190 (3): 833–40. doi:10.1534/genetics.112.138438. PMC 3296251. PMID 22419076.