Abstract

By screening approximately 10(6) plaques in a wheat DNA library with a "full-length" germin cDNA probe, two genomic clones were detected. When digested with EcoRI, one clone yielded a 2.8-kilobase pair fragment (gf-2.8) and the other yielded a 3.8-kilobase pair fragment (gf-3.8). By nucleotide sequencing, each of gf-2.8 and gf-3.8 was found to encode a complete sequence for germin and germin mRNA, and to contain appreciable amounts of 5'- and 3'-flanking sequences. The "cap" site in gf-2.8 was determined by primer extension and the corresponding site in gf-3.8 was deduced by analogy. The mRNA coding sequences in gf-2.8 and gf-3.8 are intronless and 87% homologous with one another. The 5'-flanking regions in gf-2.8 and gf-3.8 contain recognizable sites of what are probably cis-acting elements but there is otherwise little if any significant similarity between them. In addition to putative TATA and CAAT boxes in the 5'-flanking regions of gf-2.8 and gf-3.8, there are AT-rich inverted-repeats, GC boxes, long purine-rich sequences, two 19-base pair direct-repeat sequences in gf-2.8, and a remarkably long (200-base pair) inverted-repeat sequence (approximately 90% homology) in gf-3.8. An 8% difference between the mature-protein coding regions in gf-2.8 and gf-3.8 is reflected by a corresponding 7% difference between the corresponding 201-residue proteins. Most significantly, the same 8% difference between the mature-protein coding regions in gf-2.8 and gf-3.8 is allied with no change whatever in a central part (61-151) of the encoded polypeptide sequences. It seems likely that this central, strongly conserved core in the germins is of first importance in the biochemical involvements of the proteins. When an equivalence is assumed between like amino acids, the gf-2.8 and gf-3.8 germins show significant (approximately 44%) similarity to spherulins 1a and 1b of Physarum polycephalum, a similarity that increases to approximately 50% in the conserved core of germin. Near the middle (87-96) of the conserved core in the germins is a rare PH(I/T)HPRATEI decapeptide sequence which is shared by spherulins (1a and 1b) and germins (gf-2.8 and gf-3.8). These similarities are discussed in the context of evidence which can be interpreted to suggest that the biochemistry of germins and spherulins is involved with cellular, perhaps cell-wall responses to desiccation, hydration, and osmotic stress.(ABSTRACT TRUNCATED AT 400 WORDS)

Highlights

  • Was found to encode a complete sequence for germin and germin mRNA, and to contain appreciable amounts of 5’- and 3”flanking sequences

  • It is apparent that investigations of the biochemistry and molecular biology of germin have expanding consequenfcoer studies of other cereals, other organisms, and disparatebiological phenomena

  • This discussion of our current findingswill he subdivided into two parts, one that deals with thme olecular biology of cereal development, and another which deals with what appear to he germin-related processes in closely and distantly related organisms

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Summary

Family Germin Gene

A virtually full-length germin cDNA waissolated (Rahman et al, 1988) and its polynucleotide sequence was determined (Dratewka-Kos et al, 1989). 7H20,5 ml of 1M Tris chloride (pH 7.5), 0.5ml of 2% gelatin in 100 ml of water) and the diluted library (50 pl) was mixed with 300 pl of ED8767 in 10-ml Falcon tubes for incubation at 37 "C (2 h) before this study, germin cDNA has been used to detect genomic being mixed with 6.5 ml of top-agarose (0.7%) and poured over clones by screening -lo plaques in a wheat DNA library (Murray et al, 1984). The mRNA scribe single-strand templates.Full sequences were deduced from the sequence of gf-2.8 is identical with that previously determined overlaps obtained when deoxyribonucleotide sequences were deter- for a virtually full-length germin cDNA (Dratewka-Kos et ai., mined for (-70% of) each strand of the gf-2.8 and gf-3.8 clones

RESULTS
CTC A A I TCCAAG
Findings
DISCUSSION
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