Isolation of inner cell masses from mouse blastocysts by immunosurgery or exposure to the calcium ionophore A23187.

Two techniques have been evaluated for their use in routinely isolating inner cell masses from mouse blastocysts by destroying the trophectoderm. The most efficient method of immunosurgery was a 15-min incubation in a 1:50 dilution of rabbit anti-mouse spleen antiserum followed by a 30--60-min incubation in guinea pig complement (1:10). Alternatively, inner cell masses were isolated by incubating blastocysts in 10(-5) M calcium ionophore A23187 in medium devoid of calcium and magnesium ions. Inner cell masses re-exposed to immunosurgery or the ionophore were less susceptible to lysis than the trophectoderm had been. The presence of the zona pellucida reduced trophectoderm lysis by immunosurgery in antiserum dilutions greater than 1:100, but had no effect when in the presence of ionophore. Inner cell masses were consistently isolated from expanded blastocysts which had been collected 78 h after ovulation and cultured in vitro for 24 h before exposure to ionophore or immunosurgery, whereas blastocysts which had developed for the full 102 h in vivo were frequently unaffected.     

The retinoblastoma protein is phosphorylated during specific phases of the cell cycle

p105-RB is the product of the retinoblastoma tumor suppressor gene. It is a nuclear phosphoprotein hypothesized to act as an inhibitor of cellular proliferation, yet surprisingly it is present in actively dividing cells. To look for changes in p105-RB that may regulate its activity during the cell cycle, we generated synchronized cell populations and followed their progression through the cell cycle. p105-RB is synthesized throughout the cycle, but is phosphorylated in a phase-specific manner. In the G0 and G1 phases of the cell cycle, an unphosphorylated species of the protein is the only detectable form, whereas in the S and G2/M phases, multiple phosphorylated species of p105-RB are detected.     

Ecological divergence among sympatric colour morphs in blood pythons, Python brongersmai

Blood pythons in northeastern Sumatra display a series of discrete colour morphs, even among hatchlings within a single clutch. The first step towards understanding the maintenance of this polymorphism is to test the null hypothesis that colour variation in this species has no major biological correlates. Data on >2,000 blood pythons killed for the commercial leather industry enabled us to test, and reject, this hypothesis. The four colour morphs differed significantly in most of the traits that we measured, including temporal and spatial abundances, sex ratios, age structures, mean adult body sizes, body shapes (tail length and body mass relative to snout-vent length), energy stores, numbers of gut parasites, prey types, feeding frequencies and clutch sizes. The causal basis for these associations remains unclear, but is likely to involve three processes: direct effects of colour, linkages between genes for colour and other traits, and correlated spatial heterogeneity in colour, morphology and ecology. The colour polymorphism may be maintained by frequency-dependent selection and genotype-specific habitat selection, because these sedentary ambush predators are under strong selection for effective camouflage to hide them from both predators and potential prey. In support of this hypothesis, similar colour polymorphisms have evolved independently in several other snake taxa that rely upon ambush predation. Received: 18 December 1997 / Accepted: 23 March 1998