Crossover interference explained

Crossover interference is the term used to refer to the non-random placement of crossovers with respect to each other during meiosis. The term is attributed to Hermann Joseph Muller, who observed that one crossover "interferes with the coincident occurrence of another crossing over in the same pair of chromosomes, and I have accordingly termed this phenomenon ‘interference’."[1]

Meiotic crossovers (COs) appear to be regulated to ensure that COs on the same chromosome are distributed far apart (crossover interference). In the nematode worm Caenorhabditis elegans, meiotic double-strand breaks (DSBs) outnumber COs. Thus not all DSBs are repaired by a recombination process(es) leading to COs. The RTEL-1 protein is required to prevent excess meiotic COs. In rtel-1 mutants meiotic CO recombination is significantly increased and crossover interference appears to be absent.[2] RTEL1 likely acts by promoting synthesis-dependent strand annealing which results in non-crossover (NCO) recombinants instead of COs (see diagram). Normally, about half of all DSBs are converted into NCOs. RTEL-1 appears to enforce meiotic crossover interference by directing the repair of some DSBs towards NCOs rather than COs.

In humans, recombination rate increases with maternal age.[3] Furthermore, placement of female recombination events appears to become increasingly deregulated with maternal age, with a larger fraction of events occurring within closer proximity to each other than would be expected under simple models of crossover interference.[4]

High negative interference

Bacteriophage T4

High negative interference (HNI), in contrast to positive interference, refers to the association of recombination events ordinarily measured over short genomic distances, usually within a gene. Over such short distances there is a positive correlation (negative interference) of recombinational events. As studied in bacteriophage T4 this correlation is greater the shorter the interval between the sites used for detection.[5] HNI is due to multiple exchanges within a short region of the genome during an individual mating event.[6] What is counted as a “single exchange” in a genetic cross involving only distant markers may in reality be a complex event that is distributed over a finite region of the genome.[7] Switching between template DNA strands during DNA synthesis (see Figure, SDSA pathway), referred to as copy-choice recombination, was proposed to explain the positive correlation of recombination events within the gene.[8] HNI appears to require fairly precise base complementarity in the regions of the parental genomes where the associated recombination events occur.[9]

HIV

Each human immunodeficiency virus (HIV) particle contains two single-stranded positive sense RNA genomes. After infection of a host cell, a DNA copy of the genome is formed by reverse transcription of the RNA genomes. Reverse transcription is accompanied by template switching between the two RNA genome copies (copy-choice recombination).[10] From 5 to 14 recombination events per genome occur at each replication cycle.[11] This recombination exhibits HNI.[12] HNI is apparently caused by correlated template switches during minus-strand DNA synthesis.[13] Template switching recombination appears to be necessary for maintaining genome integrity and as a repair mechanism for salvaging damaged genomes.[10] [14]

Notes and References

  1. Muller, H.J. . The mechanism of crossing over . Am. Nat. . 50 . 1916.
  2. Youds JL, Mets DG, McIlwraith MJ, Martin JS, Ward JD, ONeil NJ, Rose AM, West SC, Meyer BJ, Boulton SJ . RTEL-1 enforces meiotic crossover interference and homeostasis . Science . 327 . 5970 . 1254–8 . 2010 . 20203049 . 10.1126/science.1183112 . 4770885.
  3. Kong A, Barnard J, Gudbjartsson DF, Thorleifsson G, Jonsdottir G, Sigurdardottir S, Richardsson B, Jonsdottir J, Thorgeirsson T, Frigge ML, Lamb NE, Sherman S, Gulcher JR, Stefansson K . Recombination rate and reproductive success in humans . Nat. Genet. . 36 . 11 . 1203–6 . 2004 . 15467721 . 10.1038/ng1445 . free .
  4. Campbell CL, Furlotte NA, Eriksson N, Hinds D, Auton A . Escape from crossover interference increases with maternal age . Nat Commun . 6 . 6260 . 2015 . 25695863 . 4335350 . 10.1038/ncomms7260 .
  5. Chase M, Doermann AH . High Negative Interference over Short Segments of the Genetic Structure of Bacteriophage T4 . Genetics . 43 . 3 . 332–53 . May 1958 . 17247760 . 1209884 . 10.1093/genetics/43.3.332 .
  6. Edgar RS, Steinberg CM . On the origin of high negative interference over short segments of the genetic structure of bacteriophage T4 . Virology . 6 . 1 . 115–28 . August 1958 . 13626191 . 10.1016/0042-6822(58)90063-1 .
  7. Steinberg CM, Edgar RS . A critical test of a current theory of genetic recombination in bacteriophage . Genetics . 47 . 2 . 187–208 . February 1962 . 13916671 . 1210322 . 10.1093/genetics/47.2.187 .
  8. H. . Bernstein . On the mechanism of intragenic recombination. I. The rII region of bacteriophage T4 . Journal of Theoretical Biology . 3 . 335–353 . 1962 . 10.1016/S0022-5193(62)80030-7 .
  9. Berger H, Warren AJ . Effects of deletion mutations on high negative interference in T4D bacteriophage . Genetics . 63 . 1 . 1–5 . September 1969 . 5365292 . 1212323 . 10.1093/genetics/63.1.1 .
  10. Rawson JM, Nikolaitchik OA, Keele BF, Pathak VK, Hu WS . Recombination is required for efficient HIV-1 replication and the maintenance of viral genome integrity . Nucleic Acids Res . 46 . 20 . 10535–45 . November 2018 . 30307534 . 6237782 . 10.1093/nar/gky910 .
  11. Cromer D, Grimm AJ, Schlub TE, Mak J, Davenport MP . Estimating the in-vivo HIV template switching and recombination rate . AIDS . 30 . 2 . 185–92 . January 2016 . 26691546 . 10.1097/QAD.0000000000000936 .
  12. Hu WS, Bowman EH, Delviks KA, Pathak VK . Homologous recombination occurs in a distinct retroviral subpopulation and exhibits high negative interference . J Virol . 71 . 8 . 6028–36 . August 1997 . 9223494 . 191860 . 10.1128/JVI.71.8.6028-6036.1997 .
  13. Anderson JA, Teufel RJ, Yin PD, Hu WS . Correlated template-switching events during minus-strand DNA synthesis: a mechanism for high negative interference during retroviral recombination . J Virol . 72 . 2 . 1186–94 . February 1998 . 9445017 . 124595 . 10.1128/JVI.72.2.1186-1194.1998 .
  14. Hu WS, Temin HM . Retroviral recombination and reverse transcription . Science . 250 . 4985 . 1227–33 . November 1990 . 1700865 . 10.1126/science.1700865 .