Take the 2-minute tour ×
Biology Stack Exchange is a question and answer site for biology researchers, academics, and students. It's 100% free, no registration required.

I have heard that during meiosis, homologous chromosomes from each parent "cross-over", which enables the off-spring to inherit some alleles from the mother and some alleles from the father. The picture below illustrates this "cross-over", but of course this must occur at multiple sites, rather than just the one shown in the picture.

enter image description here

Now my question is what causes the chromosomes to align perfectly during cross-over so that the loci of a particular gene will substitute for the corresponding loci on the homologous chromosome, as opposed to being substituted with a completely random locus? Does each gene have a unique non coding sequence before it specifying what gene it is to enable this process to occur?

share|improve this question
You might enjoy reading the section on crossing over from Bruce Alberts' The Cell. I love that book as it has answers to many beautiful questions that may arise regarding cell biology. –  biogirl Apr 26 '14 at 16:41

1 Answer 1

up vote 4 down vote accepted

Quite simply, because chromosome pairing is sequence specific. Holliday Junctions, which are the functional structures of a cross-over, occur through a process called "strand invasion," during which a region of one chromosome physically base-pairs with that of another. Thus one locus cannot pair with a random locus, as there is generally insufficient sequence complimentarity between two random regions to form a functional Holliday Junction. One interesting consequence of this mechanism is gene duplication and deletion in repetitious regions of the chromosome. For example, genes with large repeated regions, such as the gene responsible for Huntington's disease, can expand and contract during homologous recombination due to strand invasion occurring at non-equivalent, but still homologous, sites. Wikipedia does a nice job going over homologous recombination. I also recommend looking over the relevant sections in Molecular Biology of the Cell, available on the PubMed Bookshelf.

share|improve this answer
Most of the time sequence differences between alleles are quite small. Two genes with large changes between them are not alleles, they're homologs. Alleles tend to have one or a few Single Nucleotide Polymorphisms (SNPs) that distinguish them. For example, the gene that causes sickle cell anemia, differs from the wild type allele by only a single base change. nature.com/scitable/topicpage/genetic-mutation-441. These very small changes are irrelevant in the context of a 10 Kb cross over. –  Richard Rymer Apr 26 '14 at 13:40

Your Answer


By posting your answer, you agree to the privacy policy and terms of service.

Not the answer you're looking for? Browse other questions tagged or ask your own question.