The mouse Brachyury the Second (T2) gene is 15 kb away from classical
Brachyury (T). A mutation in T2 disrupts notochord development, pointi
ng to the existence of a second T/t complex gene involved in axis deve
lopment. T2 encodes a novel protein that is disrupted by an insertion
in T2(Bob) mice. Sequence analysis of T2 from several t haplotypes sho
ws that they all share the same changed stop codon, and, thus, T2 is a
candidate gene for the t complex tail interaction factor. T1, T2, and
the unlinked t-int are distinct and unrelated loci, and mutations in
these genes do not complement one another genetically. Either their pr
oducts interact in the same pathway during the genesis of the embryoni
c axis, or the T/t region itself is truly complex.