H. Hayes et al., Localization by FISH of the 31 Texas nomenclature type I markers to both Q- and R-banded bovine chromosomes, CYTOG C GEN, 90(3-4), 2000, pp. 315-320
A series of 31 marker genes (one per chromosome) were localized precisely t
o both Q- and R-banded bovine chromosomes by fluorescence in situ hybridiza
tion (FISH), as a contribution to the revised chromosome nomenclature of th
e three major domestic bovidae (cattle, sheep and goat). All marker genes e
xcept one (LDHA) are taken from the Texas Nomenclature of the cattle karyot
ype published in 1996. Homologous probes for each marker gene were obtained
by screening a bovine BAC library by PCR with specific primer pairs. After
labeling with biotin, each probe preparation was divided into two fraction
s and hybridized to bovine chromosomes identified either by Q or R banding.
Clear signals and good quality band patterns were observed in all cases. R
esults of the two series of hybridizations are totally concordant both for
Q and R band chromosome numbering and precise band localization. This work
permits an unambiguous correlation between the Q/G- and R-banded 31 bovine
chromosomes, including chromosomes 25, 27 and 29 which remained unresolved
in the Texas Nomenclature (1996). Hybridization of the chromosome 29 marker
gene to metaphase spreads from a 1;29 Robertsonian translocation bull carr
ier showed a positive signal on the short arm of this rearranged chromosome
, confirming that the numbering of this long-known translocation in cattle
is correct when referring to the Texas Nomenclature (1996). Taking into acc
ount that cattle, goat and sheep have very similar banded karyotypes, the d
ata presented here will help to establish a definite and complete reference
chromosome nomenclature for these species. Copyright (C) 2000 S. Karger AG
, Basel.