Ovigerous-hair stripping substance (OHSS) in an estuarine crab: Purification, preliminary characterization, and appearance of the activity in the developing embryos
M. Saigusa et H. Iwasaki, Ovigerous-hair stripping substance (OHSS) in an estuarine crab: Purification, preliminary characterization, and appearance of the activity in the developing embryos, BIOL B, 197(2), 1999, pp. 174-187
Ovigerous-hair stripping substance (OHSS) is an active factor in crab hatch
water (i.e., filtered medium into which zoea larvae have been released). T
his factor participates in stripping off the egg attachment structures (i.e
., egg case, funiculus, and the coat investing ovigerous hairs) that remain
attached to the female's ovigerous hairs after larval release. Thus this a
ctivity prepares the hairs for the next clutch of embryos. OHSS activity of
an estuarine crab, Sesarma haematocheir, eluted as a single peak on molecu
lar-sieve chromatography, but this peak still showed halo protein bands at
32 kDa and 30 kDa on SDS-PAGE. The two protein bands stained with a polyclo
nal antiserum raised to the active fractions from molecular-sieve chromatog
raphy. Moreover, antibodies purified from this polyclonal OHSS antiserum al
so recognized both the 32-kDa and 30-kDa bands. OHSS immunoreactivity and b
iological activity were associated with the attachment structures that rema
ined connected to the ovigerous hairs after hatching. In developing embryos
,both protein bands could be stained immunochemically at least 10 days befo
re hatching. But OHSS biological activity appeared only 3 days before hatch
ing. The immunoreactive protein bands were nor observed in the zoea, but OH
SS bioreactivity was present, though greatly reduced. The 32-kDa protein, a
t least, is probably an active OHSS, and the 30-kDa protein band may also b
e OHSS-related. The OHSS appears to be produced and stored by the developin
g embryo. Upon hatching, most of the material may be trapped by the remnant
structures, and the remainder is released into the ambient water.